About Exogene At Exogene, we're reimagining what's possible in cancer immunotherapy. Our mission is to engineer T-cell receptor therapies that can precisely and powerfully target solid tumours-diseases long considered out of reach for conventional immunotherapies. To do this, we've built a proprietary lab-in-the-loop platform that merges generative AI, biophysical modelling, and high-throughput TCR screening to rapidly design, test, and optimise TCRs with exceptional affinity and specificity. This convergence of computation and wet-lab experimentation allows us to go from concept to candidate molecules in record time. We're developing trispecific TCR-based T cell engagers (TCR-TriTCEs) -a new therapeutic modality designed to overcome the unique challenges of the solid tumour microenvironment. This work spans multiple disciplines, from protein engineering and AI-driven design to in vivo validation and translational development. We are looking for a dynamic senior or principal scientist who will help drive the TCR engineering processes and development. The successful candidate will leadin vivo andin vitrovalidation of TCEs. You'll get involved in purifying recombinant TCRs to perform high-throughput TCR display methods and deep sequencing. Responsibilities Lead in vivo and in vitro validation of TCEs. Collaboratively design and characterise TCRs for proprietary and partnered disease targets. Conduct a suite of protein science operations, including expression, purification, and biophysical analysis. Tackle molecular biology duties: cloning, mutagenesis, DNA isolation, and preparing libraries for deep sequencing. Manage tissue culture assignments, spanning from media prep and cell line care to cryopreservation. Join forces with founders, R&D, academia, and industrial stakeholders to fulfil ambitious R&D objectives. Draft, revise, and oversee repertoire of lab protocols. Offer essential lab support and uphold facility upkeep. Skills and Qualifications PhD in Immunology, Cell Biology, Biochemistry, or an alike field, paired with at least 1-2 years of relevant lab experience is required. For senior scientist we are looking for over 3 years industry experience. Experience in in vivo and in vitro validation of TCEs (T-cell engagers) all the way though to investigational new drug (IND) approval is critical. Knowledge of molecular biology protocols, with an emphasis on cloning and PCR is preferred. A background in protein expression, purification and biophysical characterisation is preferred. Experience in cell and immunological assays (flow cytometry, ELISA etc.) is desired. Experience in NGS analysis pipeline (specifically data analysis using software such as R) is desired. SOP documentation experience is desired. The highest standards in lab precision, record maintenance, and documentation. Excellent written and oral communication skills. Attributes Self-starter with sound analytical skills, who values scientific integrity and novelty. Collaborative spirit within the lab, open to both giving and receiving actionable feedback. Exceptional at diagnosing and overcoming unforeseen technical challenges. Adept at juggling and prioritising multiple projects to meet deadlines. Versatile and efficient within an interdisciplinary, fast-paced team setup. What We Offer Market-competitive salary and stock option package. A generous leave policy: 25 days holiday, public holidays, plus a day off for your birthday! Access to fully equipped private lab. Flexibility to work from home as project demands allow. A supportive, cross-disciplinary team fostering a highly collaborative work environment. How to apply Please send your CV and cover letter (max 400 words) to m.hasan at exogene.co.uk
Aug 14, 2025
Full time
About Exogene At Exogene, we're reimagining what's possible in cancer immunotherapy. Our mission is to engineer T-cell receptor therapies that can precisely and powerfully target solid tumours-diseases long considered out of reach for conventional immunotherapies. To do this, we've built a proprietary lab-in-the-loop platform that merges generative AI, biophysical modelling, and high-throughput TCR screening to rapidly design, test, and optimise TCRs with exceptional affinity and specificity. This convergence of computation and wet-lab experimentation allows us to go from concept to candidate molecules in record time. We're developing trispecific TCR-based T cell engagers (TCR-TriTCEs) -a new therapeutic modality designed to overcome the unique challenges of the solid tumour microenvironment. This work spans multiple disciplines, from protein engineering and AI-driven design to in vivo validation and translational development. We are looking for a dynamic senior or principal scientist who will help drive the TCR engineering processes and development. The successful candidate will leadin vivo andin vitrovalidation of TCEs. You'll get involved in purifying recombinant TCRs to perform high-throughput TCR display methods and deep sequencing. Responsibilities Lead in vivo and in vitro validation of TCEs. Collaboratively design and characterise TCRs for proprietary and partnered disease targets. Conduct a suite of protein science operations, including expression, purification, and biophysical analysis. Tackle molecular biology duties: cloning, mutagenesis, DNA isolation, and preparing libraries for deep sequencing. Manage tissue culture assignments, spanning from media prep and cell line care to cryopreservation. Join forces with founders, R&D, academia, and industrial stakeholders to fulfil ambitious R&D objectives. Draft, revise, and oversee repertoire of lab protocols. Offer essential lab support and uphold facility upkeep. Skills and Qualifications PhD in Immunology, Cell Biology, Biochemistry, or an alike field, paired with at least 1-2 years of relevant lab experience is required. For senior scientist we are looking for over 3 years industry experience. Experience in in vivo and in vitro validation of TCEs (T-cell engagers) all the way though to investigational new drug (IND) approval is critical. Knowledge of molecular biology protocols, with an emphasis on cloning and PCR is preferred. A background in protein expression, purification and biophysical characterisation is preferred. Experience in cell and immunological assays (flow cytometry, ELISA etc.) is desired. Experience in NGS analysis pipeline (specifically data analysis using software such as R) is desired. SOP documentation experience is desired. The highest standards in lab precision, record maintenance, and documentation. Excellent written and oral communication skills. Attributes Self-starter with sound analytical skills, who values scientific integrity and novelty. Collaborative spirit within the lab, open to both giving and receiving actionable feedback. Exceptional at diagnosing and overcoming unforeseen technical challenges. Adept at juggling and prioritising multiple projects to meet deadlines. Versatile and efficient within an interdisciplinary, fast-paced team setup. What We Offer Market-competitive salary and stock option package. A generous leave policy: 25 days holiday, public holidays, plus a day off for your birthday! Access to fully equipped private lab. Flexibility to work from home as project demands allow. A supportive, cross-disciplinary team fostering a highly collaborative work environment. How to apply Please send your CV and cover letter (max 400 words) to m.hasan at exogene.co.uk
Head of COA Regulatory Strategy, Patient Centered Solutions page is loaded Head of COA Regulatory Strategy, Patient Centered Solutions Apply locations Reading, Berkshire, United Kingdom time type Full time posted on Posted Yesterday job requisition id R IQVIA provides scientific services spanning clinical trials, real world evidence, and consulting in all areas of the medical product lifecycle. The Patient Centered Solutions (PCS) team leads the industry in generating data to ensure that the patient voice is incorporated into the development and commercialization of medication and other drug/non-drug interventions. We focus on understanding and meeting the needs of our customers (mostly life science/pharmaceutical companies) through the application of broad consulting expertise and technical scientific knowledge to design scientifically rigorous research to capture insights about patient priorities, needs, preferences and experiences. This research is broad and includes qualitative (e.g., interviews, focus groups), quantitative (e.g., clinical outcome assessments COAs /patient-reported outcomes PROs , preference research) and passive (e.g., digital health technology tools) approaches to understand patient, caregiver and healthcare professional experiences and expectations of disease and treatment. Individuals joining us are assured of a rewarding and progressive career in life sciences consulting. They have the opportunity to address challenging client issues, across multiple geographies with a hands-on influence in delivering solutions. We operate in a truly multi-cultural, collegial, and collaborative work environment that is rich in development and growth. Role & Responsibilities The Head of the Center of Excellence (CoE) for Regulatory Strategy sits within the COA consulting business of PCS and plays a key role in its global leadership team. This individual is a true expert in both the guidance and the practice of developing strategies to engage US FDA, the EMA and other regulatory agencies on COA endpoints and the use of Patient Experience Data (PED) in a regulatory context. This individual fulfills three key functions: 1) bringing their own expertise to bear in proposals, to project delivery, and to customers in support of business growth and impact; 2) developing the regulatory capabilities of the PCS consulting organization through training, process improvement and mentorship; and 3) maintaining an active external profile and involvement in the regulatory landscape for PED. Key responsibilities are: Customer-facing activities Develop and deliver insightful, value-added regulatory strategies that address complex client issues relating to COA endpoints and PED Support sales efforts by providing regulatory subject matter expertise to customer meetings and proposals Support delivery teams who are executing PCS projects with a regulatory component, and ensure we provide consistently high quality insights and content Support billable projects as SME and/or study lead, per study requirements, at 40% utilization or greater Capability building Support community building with activities including recruitment, coaching, management of resources and network development (both juniors and seniors) to collaborate with for regulatory delivery and/or business development purposes Directly line manage a small global team of regulatory specialists Mentor, coach, and share subject matter expertise with others to help develop individuals and capabilities delivering world-class solutions for clients Provide training, templates, and oversight to upskill team and ensure consistent high quality consulting and written deliverables Participate in annual performance review team processes Engage in recruitment and selection of new staff External profile Develop and oversee the PCS thought leadership agenda for the regulatory capability. Represent IQVIA in external working groups and consortia Lead development of IQVIA's responses to public consultation processes from FDA and other regulatory agencies relating to PED Contribute to the enhanced awareness of PCS in the marketplace, e.g., through speaking engagements, client meetings, and publications Develop and facilitate understanding of emerging regulatory practices, expectations and engagements outside of the US FDA and EMA In addition, take on other leadership responsibilities as needed, including: Member of global PCS consulting leadership team and scientific leadership team Provide regulatory subject matter expertise related to PED to the broader PCS organisation (e.g. to instrument ownership and licensing business, and to the implementation services business) About You Candidates interested this position will have: Advanced degrees and 15+ years of experience in PED research, including COA science, preference research, and regulatory engagement (US FDA essential, EMA and other regulatory agencies desirable) Experience working in a regulatory agency and/or demonstrable track record of developing and executing a COA endpoint strategy with successful outcome of COA label claim Experience preparing for, and participating in Type B and Type C meetings with FDA Experience in developing patient experience materials for regulatory consultations and submissions (e.g. COA dossier, briefing documents for Type B/C/D consultations) An understanding of the global regulatory environment as it pertains to PED Strong scientific consulting skills and track record of contributing to business development in a consulting environment Experience of medical writing for various audiences, including pharmaceutical companies, healthcare professionals, regulatory bodies and patients Publications and recognition in the field through participation in industry consortia or scientific bodies. Experienced public speaker Well-developed written and verbal communication skills including presentations, business and report writing An entrepreneurial nature and interest in developing new client offerings and solutions Demonstrable analytical, interpretative, and problem-solving skills Excellent interpersonal skills and ability to work effectively with others An ability to work in a fast-paced environment with demonstrated ability to effectively manage multiple tasks An ability to establish and maintain effective working relationships in multi-disciplinary and international teams Fluency in English (spoken and written) Willingness and ability to travel from time to time Right to live and work in the recruiting country Physical requirements: Extensive use of telephone communication requiring accurate perception of speech. Extensive use of keyboard requiring repetitive motion of fingers. Regular sitting for extended periods of time. Travel as required. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide . Learn more at Similar Jobs (3) Director, COA Management, Patient Centered Solutions locations 2 Locations time type Full time posted on Posted 20 Days Ago Global Trial Manager, Late Phase Studies, Single-Sponsor Dedicated (home-based in Europe) locations 6 Locations time type Full time posted on Posted 7 Days Ago Clinical Biospecimen Scientist - sponsor dedicated (home-based) locations 2 Locations time type Full time posted on Posted Yesterday
Aug 14, 2025
Full time
Head of COA Regulatory Strategy, Patient Centered Solutions page is loaded Head of COA Regulatory Strategy, Patient Centered Solutions Apply locations Reading, Berkshire, United Kingdom time type Full time posted on Posted Yesterday job requisition id R IQVIA provides scientific services spanning clinical trials, real world evidence, and consulting in all areas of the medical product lifecycle. The Patient Centered Solutions (PCS) team leads the industry in generating data to ensure that the patient voice is incorporated into the development and commercialization of medication and other drug/non-drug interventions. We focus on understanding and meeting the needs of our customers (mostly life science/pharmaceutical companies) through the application of broad consulting expertise and technical scientific knowledge to design scientifically rigorous research to capture insights about patient priorities, needs, preferences and experiences. This research is broad and includes qualitative (e.g., interviews, focus groups), quantitative (e.g., clinical outcome assessments COAs /patient-reported outcomes PROs , preference research) and passive (e.g., digital health technology tools) approaches to understand patient, caregiver and healthcare professional experiences and expectations of disease and treatment. Individuals joining us are assured of a rewarding and progressive career in life sciences consulting. They have the opportunity to address challenging client issues, across multiple geographies with a hands-on influence in delivering solutions. We operate in a truly multi-cultural, collegial, and collaborative work environment that is rich in development and growth. Role & Responsibilities The Head of the Center of Excellence (CoE) for Regulatory Strategy sits within the COA consulting business of PCS and plays a key role in its global leadership team. This individual is a true expert in both the guidance and the practice of developing strategies to engage US FDA, the EMA and other regulatory agencies on COA endpoints and the use of Patient Experience Data (PED) in a regulatory context. This individual fulfills three key functions: 1) bringing their own expertise to bear in proposals, to project delivery, and to customers in support of business growth and impact; 2) developing the regulatory capabilities of the PCS consulting organization through training, process improvement and mentorship; and 3) maintaining an active external profile and involvement in the regulatory landscape for PED. Key responsibilities are: Customer-facing activities Develop and deliver insightful, value-added regulatory strategies that address complex client issues relating to COA endpoints and PED Support sales efforts by providing regulatory subject matter expertise to customer meetings and proposals Support delivery teams who are executing PCS projects with a regulatory component, and ensure we provide consistently high quality insights and content Support billable projects as SME and/or study lead, per study requirements, at 40% utilization or greater Capability building Support community building with activities including recruitment, coaching, management of resources and network development (both juniors and seniors) to collaborate with for regulatory delivery and/or business development purposes Directly line manage a small global team of regulatory specialists Mentor, coach, and share subject matter expertise with others to help develop individuals and capabilities delivering world-class solutions for clients Provide training, templates, and oversight to upskill team and ensure consistent high quality consulting and written deliverables Participate in annual performance review team processes Engage in recruitment and selection of new staff External profile Develop and oversee the PCS thought leadership agenda for the regulatory capability. Represent IQVIA in external working groups and consortia Lead development of IQVIA's responses to public consultation processes from FDA and other regulatory agencies relating to PED Contribute to the enhanced awareness of PCS in the marketplace, e.g., through speaking engagements, client meetings, and publications Develop and facilitate understanding of emerging regulatory practices, expectations and engagements outside of the US FDA and EMA In addition, take on other leadership responsibilities as needed, including: Member of global PCS consulting leadership team and scientific leadership team Provide regulatory subject matter expertise related to PED to the broader PCS organisation (e.g. to instrument ownership and licensing business, and to the implementation services business) About You Candidates interested this position will have: Advanced degrees and 15+ years of experience in PED research, including COA science, preference research, and regulatory engagement (US FDA essential, EMA and other regulatory agencies desirable) Experience working in a regulatory agency and/or demonstrable track record of developing and executing a COA endpoint strategy with successful outcome of COA label claim Experience preparing for, and participating in Type B and Type C meetings with FDA Experience in developing patient experience materials for regulatory consultations and submissions (e.g. COA dossier, briefing documents for Type B/C/D consultations) An understanding of the global regulatory environment as it pertains to PED Strong scientific consulting skills and track record of contributing to business development in a consulting environment Experience of medical writing for various audiences, including pharmaceutical companies, healthcare professionals, regulatory bodies and patients Publications and recognition in the field through participation in industry consortia or scientific bodies. Experienced public speaker Well-developed written and verbal communication skills including presentations, business and report writing An entrepreneurial nature and interest in developing new client offerings and solutions Demonstrable analytical, interpretative, and problem-solving skills Excellent interpersonal skills and ability to work effectively with others An ability to work in a fast-paced environment with demonstrated ability to effectively manage multiple tasks An ability to establish and maintain effective working relationships in multi-disciplinary and international teams Fluency in English (spoken and written) Willingness and ability to travel from time to time Right to live and work in the recruiting country Physical requirements: Extensive use of telephone communication requiring accurate perception of speech. Extensive use of keyboard requiring repetitive motion of fingers. Regular sitting for extended periods of time. Travel as required. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide . Learn more at Similar Jobs (3) Director, COA Management, Patient Centered Solutions locations 2 Locations time type Full time posted on Posted 20 Days Ago Global Trial Manager, Late Phase Studies, Single-Sponsor Dedicated (home-based in Europe) locations 6 Locations time type Full time posted on Posted 7 Days Ago Clinical Biospecimen Scientist - sponsor dedicated (home-based) locations 2 Locations time type Full time posted on Posted Yesterday
Site Name: UK - London - New Oxford Street Posted Date: Jul Job Purpose T his position supports, for example, one or more of the following Therapeutic Areas: Respiratory, Infectious Diseases/HIV, Hepatitis/Fibrosis, Neurology/Dementias. Provides in-depth medical/scientific expertise in the safety evaluation and risk management of key GSK assets or in clinical development and/or the post-marketing setting. Ensures scientifically sound review and interpretation of data and management of safety issues and escalates safety issues identified through the safety review process to senior management and safety governance as appropriate. Makes recommendations for the further characterization, management, and communication of safety risks. Focus on efficiency and effectiveness to meet the needs of our Patients and HCPs. Supporting the pharmacovigilance and benefit-risk management of the assigned portfolio of GSK global assets to ensure Patient Safety globally. Key Responsibilities Scientific/Medical Knowledge PV Expertise Leads Pharmacovigilance and Risk Management Planning and develops strategy for approach to evaluation of issues in the clinical matrix. Leads the safety component of global regulatory submissions. Expert evaluation skills and analytical thinking for literature review, clinical data synthesis, analysis and interpretation. Demonstrated track record of quality decision making and creative problem resolution, based on assessment of all relevant supporting and conflicting information/factors and understanding of the wider context. Demonstrates highly developed multi-tasking skills, ability to prioritise tasks and consistently delivers on deadlines, with high performance standards for quality. Explores positions and alternatives to reach mutually beneficial agreements and solutions. Cross-functional Matrix team leadership Leads safety governance by development of safety strategy and its execution for products in clinical development and post marketing settings. Anticipates, detects and addresses product safety issues (e.g., product incidents) and ensures that risk-reduction strategies are implemented appropriately. Facilitates safety governance/SRTs in the clinical development and post marketing settings by assisting in the establishment and operation of cross-functional teams in any SERM to detect and address product safety issues and ensures that risk-reduction strategies are implemented appropriately in clinical study protocols and/or product labelling. Represents GS on cross-functional Clinical Matrix Teams and/or Project Teams. Leads cross-functional ad hoc teams to address urgent and important product safety issues. Leads or participates in cross-functional process initiatives and/or Process Workstreams to drive efforts to improve adherence to regulations, data standards, quality and efficiency. Authors/participates in written standard updates (e.g., SOPs) to ensure policies and regulations are being adhered to correctly and consistently. Accountable for the escalation of issues and communication on safety matters (e.g., GSB, CHSLC, GLC, QPPV). Builds strong working relationships and displays excellent leadership skills on safety issues whilst working in a matrix team, with a demonstrated ability to lead a team in a matrix setting. Ability to coach and mentor others. Communications (verbal, written) and Influencing (internal PV Governance and External LTs) Leads presentations on recommendations or safety issues to senior staff members at the GSK Senior Governance Committees. Has the skillset to interact with confidence, credibility, and influence at all levels of the GSK organisation. In addition, is expected to represent GSK and contribute to safety related discussions at meetings with regulatory authorities, outside consultants and other companies such as licensing partners. Leads cross-functional process improvement team within GSK. Thinks tactically/strategically and takes account of the internal and external environment when considering safety issues and changes to SERM processes or business improvements. Contributes to development of long-term strategy for clinical programs. Regularly contributes innovative ideas to address new issues or improve approaches to existing operations. Leads inspection readiness and prepared as needed to support audits/inspections. Excellent communication (verbal, written) and influencing (internally and externally) skills. Why you? Basic Qualifications: We are looking for professionals with these required skills to achieve our goals: Medical degree (for Medical Director) or PhamD/PhD for Scientist Advanced experience in the Pharmaceutical or Biotech industry working in Pharmacovigilance, or Drug Safety Significant pharmacovigilance experience relating to Safety Evaluation and Risk Management, encompassing both clinical development and post-marketing activities Experience with Signal Detection and safety surveillance Knowledge/experience of international pharmacovigilance requirements (e.g., ICH, GVP modules, CIOMS initiatives) and drug development and approval processes. Experience working in large matrix organizations Why GSK? Uniting science, technology and talent to get ahead of disease together. GSK is a global biopharma company with a special purpose - to unite science, technology and talent to get ahead of disease together - so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns - as an organisation where people can thrive. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/ immunology and oncology). Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it's also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves - feeling welcome, valued, and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together. GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law. We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are. Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on or . The helpline is available from 8.30am to 12.00 noon Monday to Friday, during bank holidays these times and days may vary. Please note should your enquiry not relate to adjustments, we will not be able to support you through these channels. However, we have created a UK Recruitment FAQ guide. Click the link and scroll to the Careers Section where you will find answers to multiple questions we receive Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at
Aug 14, 2025
Full time
Site Name: UK - London - New Oxford Street Posted Date: Jul Job Purpose T his position supports, for example, one or more of the following Therapeutic Areas: Respiratory, Infectious Diseases/HIV, Hepatitis/Fibrosis, Neurology/Dementias. Provides in-depth medical/scientific expertise in the safety evaluation and risk management of key GSK assets or in clinical development and/or the post-marketing setting. Ensures scientifically sound review and interpretation of data and management of safety issues and escalates safety issues identified through the safety review process to senior management and safety governance as appropriate. Makes recommendations for the further characterization, management, and communication of safety risks. Focus on efficiency and effectiveness to meet the needs of our Patients and HCPs. Supporting the pharmacovigilance and benefit-risk management of the assigned portfolio of GSK global assets to ensure Patient Safety globally. Key Responsibilities Scientific/Medical Knowledge PV Expertise Leads Pharmacovigilance and Risk Management Planning and develops strategy for approach to evaluation of issues in the clinical matrix. Leads the safety component of global regulatory submissions. Expert evaluation skills and analytical thinking for literature review, clinical data synthesis, analysis and interpretation. Demonstrated track record of quality decision making and creative problem resolution, based on assessment of all relevant supporting and conflicting information/factors and understanding of the wider context. Demonstrates highly developed multi-tasking skills, ability to prioritise tasks and consistently delivers on deadlines, with high performance standards for quality. Explores positions and alternatives to reach mutually beneficial agreements and solutions. Cross-functional Matrix team leadership Leads safety governance by development of safety strategy and its execution for products in clinical development and post marketing settings. Anticipates, detects and addresses product safety issues (e.g., product incidents) and ensures that risk-reduction strategies are implemented appropriately. Facilitates safety governance/SRTs in the clinical development and post marketing settings by assisting in the establishment and operation of cross-functional teams in any SERM to detect and address product safety issues and ensures that risk-reduction strategies are implemented appropriately in clinical study protocols and/or product labelling. Represents GS on cross-functional Clinical Matrix Teams and/or Project Teams. Leads cross-functional ad hoc teams to address urgent and important product safety issues. Leads or participates in cross-functional process initiatives and/or Process Workstreams to drive efforts to improve adherence to regulations, data standards, quality and efficiency. Authors/participates in written standard updates (e.g., SOPs) to ensure policies and regulations are being adhered to correctly and consistently. Accountable for the escalation of issues and communication on safety matters (e.g., GSB, CHSLC, GLC, QPPV). Builds strong working relationships and displays excellent leadership skills on safety issues whilst working in a matrix team, with a demonstrated ability to lead a team in a matrix setting. Ability to coach and mentor others. Communications (verbal, written) and Influencing (internal PV Governance and External LTs) Leads presentations on recommendations or safety issues to senior staff members at the GSK Senior Governance Committees. Has the skillset to interact with confidence, credibility, and influence at all levels of the GSK organisation. In addition, is expected to represent GSK and contribute to safety related discussions at meetings with regulatory authorities, outside consultants and other companies such as licensing partners. Leads cross-functional process improvement team within GSK. Thinks tactically/strategically and takes account of the internal and external environment when considering safety issues and changes to SERM processes or business improvements. Contributes to development of long-term strategy for clinical programs. Regularly contributes innovative ideas to address new issues or improve approaches to existing operations. Leads inspection readiness and prepared as needed to support audits/inspections. Excellent communication (verbal, written) and influencing (internally and externally) skills. Why you? Basic Qualifications: We are looking for professionals with these required skills to achieve our goals: Medical degree (for Medical Director) or PhamD/PhD for Scientist Advanced experience in the Pharmaceutical or Biotech industry working in Pharmacovigilance, or Drug Safety Significant pharmacovigilance experience relating to Safety Evaluation and Risk Management, encompassing both clinical development and post-marketing activities Experience with Signal Detection and safety surveillance Knowledge/experience of international pharmacovigilance requirements (e.g., ICH, GVP modules, CIOMS initiatives) and drug development and approval processes. Experience working in large matrix organizations Why GSK? Uniting science, technology and talent to get ahead of disease together. GSK is a global biopharma company with a special purpose - to unite science, technology and talent to get ahead of disease together - so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns - as an organisation where people can thrive. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/ immunology and oncology). Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it's also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves - feeling welcome, valued, and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together. GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law. We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are. Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on or . The helpline is available from 8.30am to 12.00 noon Monday to Friday, during bank holidays these times and days may vary. Please note should your enquiry not relate to adjustments, we will not be able to support you through these channels. However, we have created a UK Recruitment FAQ guide. Click the link and scroll to the Careers Section where you will find answers to multiple questions we receive Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at
Scientist II - Raw Material Projects page is loaded Scientist II - Raw Material Projects Apply locations UK - Pencoed time type Full time posted on Posted 30+ Days Ago job requisition id R The Opportunity QuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics, creating a world-leading in vitro diagnostics company with award-winning expertise in immunoassay and molecular testing, clinical chemistry and transfusion medicine. We are more than 6,000 strong and do business in over 130 countries, providing answers with fast, accurate and consistent testing where and when they are needed most - home to hospital, lab to clinic. Our culture puts our team members first and prioritizes actions that support happiness, inspiration and engagement. We strive to build meaningful connections with each other as we believe that employee happiness and business success are linked. Join us in our mission to transform the power of diagnostics into a healthier future for all. Scientist II (Raw Material Continuity Department) As QuidelOrtho continues to grow, we are seeking to appoint a Raw Material Scientist II to join our Raw Material Continuity department in Pencoed on a 2-year fixed term contract basis. This role will work a standard days shift pattern. About QuidelOrtho, Pencoed QuidelOrtho has been manufacturing products in South Wales for over 40 years. Our state-of-the-art manufacturing facility, based in Pencoed, employs over 600 people who are involved in the manufacture and supply of clinical laboratory and immunohematology products to sites across the globe. Our Pencoed team manufacture a large menu of immunohematology products used in transfusion medicine; in addition to a large menu of immunoassay products encompassing a range of disease categories. On site we have a range of functions operating globally & locally. All our employees are working towards one common goal, to help save and improve lives through diagnostics. Your new role: As a Scientist II within our Raw Material Continuity team, you will be accountable for the technical leadership and oversight of investigations or critical raw material projects which are owned within the technical group, employing a risk-based approach to validation, ensuring product quality and performance claims are met. What You'll Be Doing: Leadership of technical projects/investigations; this can include non-conformances (NCs), root cause investigations (RCIs), cost improvement projects (CIPs), supplier or raw material technical projects which are necessary to support uninterrupted production in Operations. Ownership/oversight of change control methods and other quality documentation in line with project timelines and business needs. Conducting scientific lab operations. Lab work will include the competent use of lab equipment such as pipettes, balances and where trained, the use of other analytical instruments and QuidelOrtho end-user equipment. Ensuring compliance to all relevant GLP, GDP and EHS standards. Performing the interpretation & analysis and documentation of scientific data. Providing conclusions and recommendations to the business, based on data extracted from the investigation/project work. Represent the technical team in cross functional teams and present data to Senior Management. What You'll Need to Succeed: Degree educated in relevant Scientific discipline, or relevant experience, or extensive experience in a similar role and industry. Proven understanding of immunoassay from industry experience. Previous experience of leading projects and a track record of leading/collaborating with cross-functional teams within a regulated operational or technical environment. Knowledge of Operations/Manufacturing environments. Assumes accountability, drives accountability in others and promotes a positive, results focused attitude. Continuous improvement driven with an understanding of Lean Manufacturing and Process Excellence skills. Team player who instils trust. Highly motivated and professional individual with an ability to drive engagement and to act as a catalyst for change. Excellent situational adaptability. Ability to assimilate and quickly comprehend complex issues. Drives self and others to set high standards for delivery of results. What we offer: Competitive Salary Yearly Salary Reviews Attractive Pension Scheme Bonus Scheme Life Assurance Private Medical (If applicable) LinkedIn Learning Cycle to Work Scheme Free Onsite Gym Subsidised Canteen 25 days Holidays + 1 QuidelOrtho Day + 8 Bank Holidays (Milestone Increases Available) Employee Assistance Programme Reward & Recognition Programmes State-Of-The-Art facilities Exceptional career developmental prospects Strong culture centred around collaboration & customer focus. Welcome QuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics, creating a world-leading in vitro diagnostics company with award-winning expertise in immunoassay and molecular testing, clinical chemistry and transfusion medicine. We are more than 6,000 strong and do business in over 130 countries, providing answers with fast, accurate and consistent testing where and when they are needed most - home to hospital, lab to clinic. Our culture puts our team members first and prioritizes actions that support happiness, inspiration and engagement. We strive to build meaningful connections with each other as we believe that employee happiness and business success are linked. Join us in our mission to transform the power of diagnostics into a healthier future for all. Important: Don't see a current job opportunity that is just right for you?Take 2 minutes and create a customjob alert which will notify you when we post a position which matches your interests. It is quick and easy and will make your career search easier. or Visit the QuidelOrtho to learn about our solutions, products, and services. QuidelOrtho believes in Equal Opportunity for all and is committed to ensuring all individuals, including individuals with disabilities, have an opportunity to apply for those positions that they are interested in and qualify for without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, age, veteran status, disability, genetic information, or any other protected characteristic. QuidelOrtho is also committed to providing reasonable accommodations to qualified individuals so that an individual can perform their job related duties. If you are interested in applying for an employment opportunity and require special assistance or an accommodation to apply due to a disability, please contact us at
Aug 14, 2025
Full time
Scientist II - Raw Material Projects page is loaded Scientist II - Raw Material Projects Apply locations UK - Pencoed time type Full time posted on Posted 30+ Days Ago job requisition id R The Opportunity QuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics, creating a world-leading in vitro diagnostics company with award-winning expertise in immunoassay and molecular testing, clinical chemistry and transfusion medicine. We are more than 6,000 strong and do business in over 130 countries, providing answers with fast, accurate and consistent testing where and when they are needed most - home to hospital, lab to clinic. Our culture puts our team members first and prioritizes actions that support happiness, inspiration and engagement. We strive to build meaningful connections with each other as we believe that employee happiness and business success are linked. Join us in our mission to transform the power of diagnostics into a healthier future for all. Scientist II (Raw Material Continuity Department) As QuidelOrtho continues to grow, we are seeking to appoint a Raw Material Scientist II to join our Raw Material Continuity department in Pencoed on a 2-year fixed term contract basis. This role will work a standard days shift pattern. About QuidelOrtho, Pencoed QuidelOrtho has been manufacturing products in South Wales for over 40 years. Our state-of-the-art manufacturing facility, based in Pencoed, employs over 600 people who are involved in the manufacture and supply of clinical laboratory and immunohematology products to sites across the globe. Our Pencoed team manufacture a large menu of immunohematology products used in transfusion medicine; in addition to a large menu of immunoassay products encompassing a range of disease categories. On site we have a range of functions operating globally & locally. All our employees are working towards one common goal, to help save and improve lives through diagnostics. Your new role: As a Scientist II within our Raw Material Continuity team, you will be accountable for the technical leadership and oversight of investigations or critical raw material projects which are owned within the technical group, employing a risk-based approach to validation, ensuring product quality and performance claims are met. What You'll Be Doing: Leadership of technical projects/investigations; this can include non-conformances (NCs), root cause investigations (RCIs), cost improvement projects (CIPs), supplier or raw material technical projects which are necessary to support uninterrupted production in Operations. Ownership/oversight of change control methods and other quality documentation in line with project timelines and business needs. Conducting scientific lab operations. Lab work will include the competent use of lab equipment such as pipettes, balances and where trained, the use of other analytical instruments and QuidelOrtho end-user equipment. Ensuring compliance to all relevant GLP, GDP and EHS standards. Performing the interpretation & analysis and documentation of scientific data. Providing conclusions and recommendations to the business, based on data extracted from the investigation/project work. Represent the technical team in cross functional teams and present data to Senior Management. What You'll Need to Succeed: Degree educated in relevant Scientific discipline, or relevant experience, or extensive experience in a similar role and industry. Proven understanding of immunoassay from industry experience. Previous experience of leading projects and a track record of leading/collaborating with cross-functional teams within a regulated operational or technical environment. Knowledge of Operations/Manufacturing environments. Assumes accountability, drives accountability in others and promotes a positive, results focused attitude. Continuous improvement driven with an understanding of Lean Manufacturing and Process Excellence skills. Team player who instils trust. Highly motivated and professional individual with an ability to drive engagement and to act as a catalyst for change. Excellent situational adaptability. Ability to assimilate and quickly comprehend complex issues. Drives self and others to set high standards for delivery of results. What we offer: Competitive Salary Yearly Salary Reviews Attractive Pension Scheme Bonus Scheme Life Assurance Private Medical (If applicable) LinkedIn Learning Cycle to Work Scheme Free Onsite Gym Subsidised Canteen 25 days Holidays + 1 QuidelOrtho Day + 8 Bank Holidays (Milestone Increases Available) Employee Assistance Programme Reward & Recognition Programmes State-Of-The-Art facilities Exceptional career developmental prospects Strong culture centred around collaboration & customer focus. Welcome QuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics, creating a world-leading in vitro diagnostics company with award-winning expertise in immunoassay and molecular testing, clinical chemistry and transfusion medicine. We are more than 6,000 strong and do business in over 130 countries, providing answers with fast, accurate and consistent testing where and when they are needed most - home to hospital, lab to clinic. Our culture puts our team members first and prioritizes actions that support happiness, inspiration and engagement. We strive to build meaningful connections with each other as we believe that employee happiness and business success are linked. Join us in our mission to transform the power of diagnostics into a healthier future for all. Important: Don't see a current job opportunity that is just right for you?Take 2 minutes and create a customjob alert which will notify you when we post a position which matches your interests. It is quick and easy and will make your career search easier. or Visit the QuidelOrtho to learn about our solutions, products, and services. QuidelOrtho believes in Equal Opportunity for all and is committed to ensuring all individuals, including individuals with disabilities, have an opportunity to apply for those positions that they are interested in and qualify for without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, age, veteran status, disability, genetic information, or any other protected characteristic. QuidelOrtho is also committed to providing reasonable accommodations to qualified individuals so that an individual can perform their job related duties. If you are interested in applying for an employment opportunity and require special assistance or an accommodation to apply due to a disability, please contact us at
Enara Bio's purpose is to shine a light on unconventional T cell targets to develop cancer immunotherapies designed to provide lasting benefit for broad patient populations. Our proprietary EDAPT platform enables us to discover and validate novel and differentiated cancer-specific targets from the genomic dark matter, which we call Dark Antigens. We are advancing a pipeline of bispecific T-cell engagers against novel Dark Antigens and other underexploited targets for the treatment of patients with solid tumours. Enara Bio was founded in 2016 and has been well funded to invest in the build out and growth of our R&D efforts and our fantastic team. The company is based in Oxford, UK. Role Overview Enara Bio has established a best-in-classpipeline for the identification of novel, previously undiscovered antigens for development of immunotherapies, using mass spectrometry (MS)-based proteomics and immunopeptidomics. We have recently broadened the application of MS to include the characterisation of biologics and are looking to increase internal capabilities in this area. We are looking for a highly motivated senior scientist to join our team who has a passion for MS-based proteomics applied to the exciting field of immuno-oncology. The successful candidate will help in the generation of proteomics data to support the characterization of Enara Bio's novel biotherapeutics as well as supporting our ongoing antigen-discovery pipeline. This role will make a major contribution in supporting our goal of delivering impactful therapies that make a meaningful difference to patients suffering from cancer. The successful candidate will work closely with key internal and external stakeholders including academic and non-academic partners in immunobiology, biochemistry, protein characterisation and LC/MS-based disciplines. Enara Bio actively promotes a multidisciplinary collaborative approach to working, therefore effective communication is essential to this role as you will be expected to effectively communicate with our collaborators about our scientific research objectives. Key Responsibilities Provide technical leadership on various proteomics analytical workflows with experiencein different LCMS based proteomic methods (DDA, DIA, P(M)RM and intact mass spec) Drive the protein characterisation pipeline by applying various LC-MSbased techniques for our lead biotherapeutic products Support the existing immunopeptidomic and proteomic activities including the discovery and validation of targets by LC-MS Provide input for continuous development of MS-based proteomics and immunopeptidomic methodologies by working cross-functionally with Enara's protein characterisation and computational biology teams Provide technical expertise supporting the maintenance and troubleshooting of the LC-MS instrumentation Analyse, interpret and clearly communicate data to various stakeholders to support discovery and validation campaigns Contribute to a vibrant and innovative working environment where improvements and new ideas are adopted and freely shared among the teams Minimum Qualifications and Capabilities Ph.D. (or equivalent experience) in a relevant scientific discipline such as MS-based proteomics In-depth technical expertise in LC-MS based proteomics and related sample preparation Experience & Key skills: A track record of working independently and with the ability to design and execute experiments supporting the characterisation of biologics (Peptide fingerprint mapping, PTM analysis, disulfide bridge mapping and host cell proteomics (HCP) analysis etc) Proven ability to develop and maintain high resolution LC-MS instrumentation and use of proteomics software tools (such as PEAKS, DIANN, Skyline etc) Experience of working with Bispecifics and/or mAb's would be advantageous Experience with developing and troubleshooting complimentary protein characterisation techniques (IEX, HIC, SEC) Experience with sample preparation for proteomics analysis from biological samples including tissues and cell lines with knowledge of different enrichment strategies Effective communication, both written and verbal, with a good attention to detail Self-motivated and enthusiastic team player with experience of working in cross-functional teams and proven ability to work to specific deadlines Desirable Experience of LC-MS based immunopeptidomics An understanding of the regulatory environment around biotherapeutics (ICH Q6B, ICH Q2 etc) Experience using R for data interrogation Cell culture experience Further information: The Enara Bio team is driven to make a meaningful difference for people affected by cancer. Our culture is defined by our behavioural ethos: Empowerment: We promote autonomy across Enara rejecting conventional hierarchy. We engage each other through transparency, collaboration and trust. We each take action with a deep sense of personal and shared accountability. Courage: We push boundaries in all that we do to deliver on our purpose. We make bold decisions, embrace risk and tackle challenges to advance our novel science. Courage is essential for everything we do. Humility: We are proud of and excited by our novel science, but we acknowledge that we cannot know everything. Our curiosity drives us to continually learn from each other & the outside world irrespective of our role or title. We give and receive feedback with no room for ego. Growth: We invest in our people, culture and community to foster belonging as a foundation for success. We embrace individual development to create deeper personal fulfilment and drive stronger collective impact. We offer a competitive salary, commensurate with qualifications and experience, and a benefits package including pension and health insurance. Applicants should be able to demonstrate proof of the right to work in United Kingdom. Enara Bio Limited is an equal opportunities employer.
Aug 14, 2025
Full time
Enara Bio's purpose is to shine a light on unconventional T cell targets to develop cancer immunotherapies designed to provide lasting benefit for broad patient populations. Our proprietary EDAPT platform enables us to discover and validate novel and differentiated cancer-specific targets from the genomic dark matter, which we call Dark Antigens. We are advancing a pipeline of bispecific T-cell engagers against novel Dark Antigens and other underexploited targets for the treatment of patients with solid tumours. Enara Bio was founded in 2016 and has been well funded to invest in the build out and growth of our R&D efforts and our fantastic team. The company is based in Oxford, UK. Role Overview Enara Bio has established a best-in-classpipeline for the identification of novel, previously undiscovered antigens for development of immunotherapies, using mass spectrometry (MS)-based proteomics and immunopeptidomics. We have recently broadened the application of MS to include the characterisation of biologics and are looking to increase internal capabilities in this area. We are looking for a highly motivated senior scientist to join our team who has a passion for MS-based proteomics applied to the exciting field of immuno-oncology. The successful candidate will help in the generation of proteomics data to support the characterization of Enara Bio's novel biotherapeutics as well as supporting our ongoing antigen-discovery pipeline. This role will make a major contribution in supporting our goal of delivering impactful therapies that make a meaningful difference to patients suffering from cancer. The successful candidate will work closely with key internal and external stakeholders including academic and non-academic partners in immunobiology, biochemistry, protein characterisation and LC/MS-based disciplines. Enara Bio actively promotes a multidisciplinary collaborative approach to working, therefore effective communication is essential to this role as you will be expected to effectively communicate with our collaborators about our scientific research objectives. Key Responsibilities Provide technical leadership on various proteomics analytical workflows with experiencein different LCMS based proteomic methods (DDA, DIA, P(M)RM and intact mass spec) Drive the protein characterisation pipeline by applying various LC-MSbased techniques for our lead biotherapeutic products Support the existing immunopeptidomic and proteomic activities including the discovery and validation of targets by LC-MS Provide input for continuous development of MS-based proteomics and immunopeptidomic methodologies by working cross-functionally with Enara's protein characterisation and computational biology teams Provide technical expertise supporting the maintenance and troubleshooting of the LC-MS instrumentation Analyse, interpret and clearly communicate data to various stakeholders to support discovery and validation campaigns Contribute to a vibrant and innovative working environment where improvements and new ideas are adopted and freely shared among the teams Minimum Qualifications and Capabilities Ph.D. (or equivalent experience) in a relevant scientific discipline such as MS-based proteomics In-depth technical expertise in LC-MS based proteomics and related sample preparation Experience & Key skills: A track record of working independently and with the ability to design and execute experiments supporting the characterisation of biologics (Peptide fingerprint mapping, PTM analysis, disulfide bridge mapping and host cell proteomics (HCP) analysis etc) Proven ability to develop and maintain high resolution LC-MS instrumentation and use of proteomics software tools (such as PEAKS, DIANN, Skyline etc) Experience of working with Bispecifics and/or mAb's would be advantageous Experience with developing and troubleshooting complimentary protein characterisation techniques (IEX, HIC, SEC) Experience with sample preparation for proteomics analysis from biological samples including tissues and cell lines with knowledge of different enrichment strategies Effective communication, both written and verbal, with a good attention to detail Self-motivated and enthusiastic team player with experience of working in cross-functional teams and proven ability to work to specific deadlines Desirable Experience of LC-MS based immunopeptidomics An understanding of the regulatory environment around biotherapeutics (ICH Q6B, ICH Q2 etc) Experience using R for data interrogation Cell culture experience Further information: The Enara Bio team is driven to make a meaningful difference for people affected by cancer. Our culture is defined by our behavioural ethos: Empowerment: We promote autonomy across Enara rejecting conventional hierarchy. We engage each other through transparency, collaboration and trust. We each take action with a deep sense of personal and shared accountability. Courage: We push boundaries in all that we do to deliver on our purpose. We make bold decisions, embrace risk and tackle challenges to advance our novel science. Courage is essential for everything we do. Humility: We are proud of and excited by our novel science, but we acknowledge that we cannot know everything. Our curiosity drives us to continually learn from each other & the outside world irrespective of our role or title. We give and receive feedback with no room for ego. Growth: We invest in our people, culture and community to foster belonging as a foundation for success. We embrace individual development to create deeper personal fulfilment and drive stronger collective impact. We offer a competitive salary, commensurate with qualifications and experience, and a benefits package including pension and health insurance. Applicants should be able to demonstrate proof of the right to work in United Kingdom. Enara Bio Limited is an equal opportunities employer.
Reporting to: Senior Manager, Analytical Sciences, MSAT Location: London Job Summary We are seeking an enthusiastic Senior Scientist to join our Analytical Science & Technology (AST) group in the Manufacturing Science and Technology (MSAT) organization, specifically within the cell gene therapy sector. The successful candidate will support the verification/validation and deployment of release and stability methods for Orchard products, as well as monitoring of methods and trends. This role includes responsibilities for deviation management and change control support. Experience with in-vitro potency and safety/microbiology methods would be a plus. Key Responsibilities Assist the Analytical Sciences team within the MSAT organization to verify, validate, deploy, and manage analytical methods to ensure product quality and compliance with applicable guidelines and regulatory requirements. Support Analytical activities at CMOs and CTOs, including defining appropriate system suitability criteria and controls for assays, performing periodic assay and data reviews, and assisting with the preparation of analytical final reports and SOPs. Aid in troubleshooting and investigations into out-of-specification/trend results for drug substances, drug products, and stability programs for raw materials, ancillary products, and plasmids. Support stability studies to ensure the consistent quality and safety of products and starting material (such as plasmids). Assist in preparing and authoring quality reports and documentation related to the development, characterization, and testing of analytical methods, as well as relevant sections of CMC documentation in support of regulatory submissions and dossier amendments. Required Knowledge Knowledge in Cell and Gene Therapy analytics, particularly in areas such as lentiviral vectors, plasmids, and cell banks. Experience with microbiology and other safety analytical techniques, and cell-based potency assays. Experience with management of quality records Understanding of the verification, validation, and trending of assay performance is desirable Basic understanding of regulatory authority inspections, including both FDA and EMA inspections is desirable. Excellent Knowledge of GMP. Skills & Abilities Strong scientific and technical proficiency with an awareness of developments in novel testing technologies within the industry. Excellent attention to detail, communication, presentation, and organizational skills. Effective troubleshooting abilities and the capacity to work independently and as part of a team. Creative problem solver with the ability to operate in a fast-paced, multi-disciplinary industrial environment. Education and Experience Minimum of a BSc in a relevant scientific discipline, such as Chemistry, Biochemistry, Molecular Biology, Cell Biology, Chemical Engineering, or another relevant field. Some experience in the biotechnology or pharma industry with a focus on the verification, validation, and application of analytical methods for product development, stability and commercial release testing is preferred.
Aug 14, 2025
Full time
Reporting to: Senior Manager, Analytical Sciences, MSAT Location: London Job Summary We are seeking an enthusiastic Senior Scientist to join our Analytical Science & Technology (AST) group in the Manufacturing Science and Technology (MSAT) organization, specifically within the cell gene therapy sector. The successful candidate will support the verification/validation and deployment of release and stability methods for Orchard products, as well as monitoring of methods and trends. This role includes responsibilities for deviation management and change control support. Experience with in-vitro potency and safety/microbiology methods would be a plus. Key Responsibilities Assist the Analytical Sciences team within the MSAT organization to verify, validate, deploy, and manage analytical methods to ensure product quality and compliance with applicable guidelines and regulatory requirements. Support Analytical activities at CMOs and CTOs, including defining appropriate system suitability criteria and controls for assays, performing periodic assay and data reviews, and assisting with the preparation of analytical final reports and SOPs. Aid in troubleshooting and investigations into out-of-specification/trend results for drug substances, drug products, and stability programs for raw materials, ancillary products, and plasmids. Support stability studies to ensure the consistent quality and safety of products and starting material (such as plasmids). Assist in preparing and authoring quality reports and documentation related to the development, characterization, and testing of analytical methods, as well as relevant sections of CMC documentation in support of regulatory submissions and dossier amendments. Required Knowledge Knowledge in Cell and Gene Therapy analytics, particularly in areas such as lentiviral vectors, plasmids, and cell banks. Experience with microbiology and other safety analytical techniques, and cell-based potency assays. Experience with management of quality records Understanding of the verification, validation, and trending of assay performance is desirable Basic understanding of regulatory authority inspections, including both FDA and EMA inspections is desirable. Excellent Knowledge of GMP. Skills & Abilities Strong scientific and technical proficiency with an awareness of developments in novel testing technologies within the industry. Excellent attention to detail, communication, presentation, and organizational skills. Effective troubleshooting abilities and the capacity to work independently and as part of a team. Creative problem solver with the ability to operate in a fast-paced, multi-disciplinary industrial environment. Education and Experience Minimum of a BSc in a relevant scientific discipline, such as Chemistry, Biochemistry, Molecular Biology, Cell Biology, Chemical Engineering, or another relevant field. Some experience in the biotechnology or pharma industry with a focus on the verification, validation, and application of analytical methods for product development, stability and commercial release testing is preferred.
Senior Applied Scientist, Prime Video Commerce Science Tech Job ID: Amazon Development Centre (London) Limited Are you interested in shaping the future of movies and television? Do you want to define the next generation of how and what Amazon customers are watching? Prime Video is one of the world's leading digital video services, and we're just getting started changing the way millions of people around the world enjoy content. Now available in more than 200 countries and territories, Prime Video offers customers the broadest selection of any on-demand video service, including our critically-acclaimed Amazon Originals Series such as The Boys, The Marvelous Mrs. Maisel, The Underground Railroad; UK-produced hit Amazon Original series like Good Omens, The Grand Tour, All or Nothing: Tottenham Hotspur and forthcoming drama series like The Power, Jungle and The Rig; exclusive TV shows like Nine Perfect Strangers and Little Fires Everywhere; and movies like Coming 2 America, Borat Subsequent Moviefilm and Without Remorse plus live sport including ATP and WTA Tour and US Open Tennis, Autumn Nations rugby and Premier League football. Amazon Studios is the movies and television development and production arm of Amazon. It is our role to produce original content and license studio programs worldwide in exclusive service of Amazon's Prime Video customers. We need your passion, innovative ideas, and creativity to help take us to new heights. Do you want to work at the intersection of Engineering, Machine Learning, Data Science, and GenAI? Do you like inventing, growing and learning from the world-class engineers and scientists? If so, we want to hear from you! We are seeking a seasoned senior scientist with expertise in causal inference, reinforcement learning. multiagent systems, agenticAI as well as LLMs to join the Amazon Studios AI Labs team. This is a hybrid applied science and engineering team that is developing bleeding edge AI solutions to enhance efficiency, elevate creativity, and ultimately redefine industry standards, ensuring that every decision is accelerated by intelligence and foresight. We need your passion, innovative ideas, and creativity to help take us to new heights. Key job responsibilities We are looking for a Senior Applied Scientist with domain expertise in causal inference, reinforcement learning. multi agent systems, agentic AI as well as LLMs who will lead development of new algorithms and E2E solutions. You will be part of a team of applied scientists and software development engineers responsible for research, design, development and deployment of algorithms into production pipelines. As a technologist, you will also drive publications of original work in top-tier conferences in Machine Learning. You will be expected to deal with ambiguity! We're looking for someone with outstanding analytical abilities and someone comfortable working with cross-functional teams and systems. You must be a self-starter and be able to learn on the go. A day in the life As a senior applied scientist at Amazon, you'll be diving deep into groundbreaking ML challenges. Your typical day involves architecting large-scale ML systems, collaborating with cross-functional teams, and mentoring junior scientists. You'll start with stand-ups, then transition to developing novel CV algorithms for product features impacting millions of customers. Afternoons often include technical deep-dives, reviewing research papers, and driving technical strategy discussions with leadership. You'll work with massive datasets, optimize model performance, and ensure production readiness. We value your ability to balance scientific innovation with practical business impact while maintaining Amazon's high technical bar. About the team This role is in a team that is building a new family of AI products for Prime Video Commerce Science Tech. This team is considered strategic and has visibility with Prime Video leadership at the highest levels. The role offers a chance to build and launch new AI services from the ground up, contribute to exceeding the state of the art in machine learning (ML) technology, and work closely with an exceptional group of product, engineering, and science leaders. BASIC QUALIFICATIONS - PhD in engineering, technology, computer science, machine learning, robotics, operations research, statistics, mathematics or equivalent quantitative field - Experience programming in Java, C++, Python or related language - Experience with neural deep learning methods and machine learning - Experience in building machine learning models for business application - Experience in applied research PREFERRED QUALIFICATIONS - Experience with modeling tools such as R, scikit-learn, Spark MLLib, MxNet, Tensorflow, numpy, scipy etc. - Experience with large scale distributed systems such as Hadoop, Spark etc. Amazon is an equal opportunities employer. We believe passionately that employing a diverse workforce is central to our success. We make recruiting decisions based on your experience and skills. We value your passion to discover, invent, simplify and build. Protecting your privacy and the security of your data is a longstanding top priority for Amazon. Please consult our Privacy Notice ( ) to know more about how we collect, use and transfer the personal data of our candidates. Amazon is an equal opportunity employer and does not discriminate on the basis of protected veteran status, disability, or other legally protected status. Our inclusive culture empowers Amazonians to deliver the best results for our customers. If you have a disability and need a workplace accommodation or adjustment during the application and hiring process, including support for the interview or onboarding process, please visit for more information. If the country/region you're applying in isn't listed, please contact your Recruiting Partner. Amazon is an equal opportunity employer and does not discriminate on the basis of protected veteran status, disability, or other legally protected status.
Aug 14, 2025
Full time
Senior Applied Scientist, Prime Video Commerce Science Tech Job ID: Amazon Development Centre (London) Limited Are you interested in shaping the future of movies and television? Do you want to define the next generation of how and what Amazon customers are watching? Prime Video is one of the world's leading digital video services, and we're just getting started changing the way millions of people around the world enjoy content. Now available in more than 200 countries and territories, Prime Video offers customers the broadest selection of any on-demand video service, including our critically-acclaimed Amazon Originals Series such as The Boys, The Marvelous Mrs. Maisel, The Underground Railroad; UK-produced hit Amazon Original series like Good Omens, The Grand Tour, All or Nothing: Tottenham Hotspur and forthcoming drama series like The Power, Jungle and The Rig; exclusive TV shows like Nine Perfect Strangers and Little Fires Everywhere; and movies like Coming 2 America, Borat Subsequent Moviefilm and Without Remorse plus live sport including ATP and WTA Tour and US Open Tennis, Autumn Nations rugby and Premier League football. Amazon Studios is the movies and television development and production arm of Amazon. It is our role to produce original content and license studio programs worldwide in exclusive service of Amazon's Prime Video customers. We need your passion, innovative ideas, and creativity to help take us to new heights. Do you want to work at the intersection of Engineering, Machine Learning, Data Science, and GenAI? Do you like inventing, growing and learning from the world-class engineers and scientists? If so, we want to hear from you! We are seeking a seasoned senior scientist with expertise in causal inference, reinforcement learning. multiagent systems, agenticAI as well as LLMs to join the Amazon Studios AI Labs team. This is a hybrid applied science and engineering team that is developing bleeding edge AI solutions to enhance efficiency, elevate creativity, and ultimately redefine industry standards, ensuring that every decision is accelerated by intelligence and foresight. We need your passion, innovative ideas, and creativity to help take us to new heights. Key job responsibilities We are looking for a Senior Applied Scientist with domain expertise in causal inference, reinforcement learning. multi agent systems, agentic AI as well as LLMs who will lead development of new algorithms and E2E solutions. You will be part of a team of applied scientists and software development engineers responsible for research, design, development and deployment of algorithms into production pipelines. As a technologist, you will also drive publications of original work in top-tier conferences in Machine Learning. You will be expected to deal with ambiguity! We're looking for someone with outstanding analytical abilities and someone comfortable working with cross-functional teams and systems. You must be a self-starter and be able to learn on the go. A day in the life As a senior applied scientist at Amazon, you'll be diving deep into groundbreaking ML challenges. Your typical day involves architecting large-scale ML systems, collaborating with cross-functional teams, and mentoring junior scientists. You'll start with stand-ups, then transition to developing novel CV algorithms for product features impacting millions of customers. Afternoons often include technical deep-dives, reviewing research papers, and driving technical strategy discussions with leadership. You'll work with massive datasets, optimize model performance, and ensure production readiness. We value your ability to balance scientific innovation with practical business impact while maintaining Amazon's high technical bar. About the team This role is in a team that is building a new family of AI products for Prime Video Commerce Science Tech. This team is considered strategic and has visibility with Prime Video leadership at the highest levels. The role offers a chance to build and launch new AI services from the ground up, contribute to exceeding the state of the art in machine learning (ML) technology, and work closely with an exceptional group of product, engineering, and science leaders. BASIC QUALIFICATIONS - PhD in engineering, technology, computer science, machine learning, robotics, operations research, statistics, mathematics or equivalent quantitative field - Experience programming in Java, C++, Python or related language - Experience with neural deep learning methods and machine learning - Experience in building machine learning models for business application - Experience in applied research PREFERRED QUALIFICATIONS - Experience with modeling tools such as R, scikit-learn, Spark MLLib, MxNet, Tensorflow, numpy, scipy etc. - Experience with large scale distributed systems such as Hadoop, Spark etc. Amazon is an equal opportunities employer. We believe passionately that employing a diverse workforce is central to our success. We make recruiting decisions based on your experience and skills. We value your passion to discover, invent, simplify and build. Protecting your privacy and the security of your data is a longstanding top priority for Amazon. Please consult our Privacy Notice ( ) to know more about how we collect, use and transfer the personal data of our candidates. Amazon is an equal opportunity employer and does not discriminate on the basis of protected veteran status, disability, or other legally protected status. Our inclusive culture empowers Amazonians to deliver the best results for our customers. If you have a disability and need a workplace accommodation or adjustment during the application and hiring process, including support for the interview or onboarding process, please visit for more information. If the country/region you're applying in isn't listed, please contact your Recruiting Partner. Amazon is an equal opportunity employer and does not discriminate on the basis of protected veteran status, disability, or other legally protected status.
Job Description Our company has a rapidly growing, interdisciplinary team of scientists in London and exciting plans to expand our London presence. This will initially be at the Francis Crick Institute as part of our 'Skylab' expansion, and from 2027 in our new 'state of art' and fully integrated Research and Discovery Centre at the hub of London's knowledge Quarter. This new building will be home to approximately 180 scientists alongside other colleagues in discovery research, clinical, regulatory and business roles, including marketing, finance and administration. We have an exciting Senior Scientist opportunity for a Biochemist/pharmacologist to join our team at the Francis Crick Institute in London on a 1-year fixed term contract. Working collaboratively with our London discovery teams you will apply your skills in biochemical/biophysical assay development, data analysis, laboratory automation and detection technologies to advance therapeutic programs across the Immunology and Neuroscience therapy areas. If you are lab-focused, scientifically curious and looking to develop your skills, we'd love for you to be part of our diverse and passionate team. In this role you will: Design and execute quantitative biochemical and biophysical assays to identify, characterize, and optimize candidates for therapeutic programs aimed at Immunology/Neuroscience related diseases. Conduct molecular mechanism of action studies to understand compound efficacy and specificity, as well as the downstream impact to biology. Apply automation to functional assays to deliver impactful data at scale. Collaborate on new technology initiatives to evaluate, implement and build internal capabilities. Collaborate with our London-based disease area and genome sciences colleagues as needed to identify our next generation of drug targets. Conceptualize and enact innovative approaches to solve program objectives and issues. Manage project-specific milestones and timelines. Interpret data and communicate science and strategy to stakeholders and management. Take on increasing responsibility within the Quantitative Biosciences group and on project teams as your skills develop. What you will need: Educated to Ph.D, or BSc/MSc level with experience in biotech/pharma; experience in Neuroscience and/or Immunology would be useful but not essential. Proven ability to independently design, implement and interpret complex biochemical/biophysical assays using fluorescence and label-free technologies and associated analytical software solutions. This may include proficiency in techniques such as SPR, thermal shift, FP, TR-FRET and luminescence & absorbance-based techniques. Practical experience in the characterisation of isolated targets, which may include but not be limited to catalytic mechanism determination, compound-inhibitor mechanism of action studies and quantitative measurement of the kinetics of drug-target interactions. An ability to propose new, innovative approaches and experimental designs as needed. Experience with medium to high throughput assay-related data analysis and an appreciation for the related quantitative and statistical concepts. A flexible and collaborative approach to working across teams, projects and departments. Effective written and oral communication skills. The ability to adapt to changing priorities with a passion for innovation and problem-solving. We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another's thinking and approach problems collectively. We are an equal opportunity employer, committed to fostering an inclusive and diverse workplace. The closing date for applications will be 11:59pm on Thursday 14th August. Current Employees apply HERE Current Contingent Workers apply HERE Search Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. Employee Status: Project Temps (Fixed Term) Relocation: VISA Sponsorship: Travel Requirements: Flexible Work Arrangements: Not Applicable Shift: Valid Driving License: Hazardous Material(s): Required Skills: Adaptability, Adaptability, Assay, Assay Development, Biochemical Assays, Cell-Based Assays, Cell Culture Techniques, Clinical Immunology, Communication, Data Analysis, Detail-Oriented, Drug Target Identification, Flow Cytometry, Fluorescence, High Content Screening, Immunoassays, Immunology, Laboratory Automation, Molecular Biology, Neuroanatomy, Oral Communications, Personal Initiative, Project Management, Protein Purifications, Quantitative Assay + 3 more Preferred Skills: Job Posting End Date: 08/15/2025 A job posting is effective until 11:59:59PM on the day BEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date. Requisition ID:R359526
Aug 14, 2025
Full time
Job Description Our company has a rapidly growing, interdisciplinary team of scientists in London and exciting plans to expand our London presence. This will initially be at the Francis Crick Institute as part of our 'Skylab' expansion, and from 2027 in our new 'state of art' and fully integrated Research and Discovery Centre at the hub of London's knowledge Quarter. This new building will be home to approximately 180 scientists alongside other colleagues in discovery research, clinical, regulatory and business roles, including marketing, finance and administration. We have an exciting Senior Scientist opportunity for a Biochemist/pharmacologist to join our team at the Francis Crick Institute in London on a 1-year fixed term contract. Working collaboratively with our London discovery teams you will apply your skills in biochemical/biophysical assay development, data analysis, laboratory automation and detection technologies to advance therapeutic programs across the Immunology and Neuroscience therapy areas. If you are lab-focused, scientifically curious and looking to develop your skills, we'd love for you to be part of our diverse and passionate team. In this role you will: Design and execute quantitative biochemical and biophysical assays to identify, characterize, and optimize candidates for therapeutic programs aimed at Immunology/Neuroscience related diseases. Conduct molecular mechanism of action studies to understand compound efficacy and specificity, as well as the downstream impact to biology. Apply automation to functional assays to deliver impactful data at scale. Collaborate on new technology initiatives to evaluate, implement and build internal capabilities. Collaborate with our London-based disease area and genome sciences colleagues as needed to identify our next generation of drug targets. Conceptualize and enact innovative approaches to solve program objectives and issues. Manage project-specific milestones and timelines. Interpret data and communicate science and strategy to stakeholders and management. Take on increasing responsibility within the Quantitative Biosciences group and on project teams as your skills develop. What you will need: Educated to Ph.D, or BSc/MSc level with experience in biotech/pharma; experience in Neuroscience and/or Immunology would be useful but not essential. Proven ability to independently design, implement and interpret complex biochemical/biophysical assays using fluorescence and label-free technologies and associated analytical software solutions. This may include proficiency in techniques such as SPR, thermal shift, FP, TR-FRET and luminescence & absorbance-based techniques. Practical experience in the characterisation of isolated targets, which may include but not be limited to catalytic mechanism determination, compound-inhibitor mechanism of action studies and quantitative measurement of the kinetics of drug-target interactions. An ability to propose new, innovative approaches and experimental designs as needed. Experience with medium to high throughput assay-related data analysis and an appreciation for the related quantitative and statistical concepts. A flexible and collaborative approach to working across teams, projects and departments. Effective written and oral communication skills. The ability to adapt to changing priorities with a passion for innovation and problem-solving. We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another's thinking and approach problems collectively. We are an equal opportunity employer, committed to fostering an inclusive and diverse workplace. The closing date for applications will be 11:59pm on Thursday 14th August. Current Employees apply HERE Current Contingent Workers apply HERE Search Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. Employee Status: Project Temps (Fixed Term) Relocation: VISA Sponsorship: Travel Requirements: Flexible Work Arrangements: Not Applicable Shift: Valid Driving License: Hazardous Material(s): Required Skills: Adaptability, Adaptability, Assay, Assay Development, Biochemical Assays, Cell-Based Assays, Cell Culture Techniques, Clinical Immunology, Communication, Data Analysis, Detail-Oriented, Drug Target Identification, Flow Cytometry, Fluorescence, High Content Screening, Immunoassays, Immunology, Laboratory Automation, Molecular Biology, Neuroanatomy, Oral Communications, Personal Initiative, Project Management, Protein Purifications, Quantitative Assay + 3 more Preferred Skills: Job Posting End Date: 08/15/2025 A job posting is effective until 11:59:59PM on the day BEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date. Requisition ID:R359526
We believe in the power of ingenuity to build a positive human future. As strategies, technologies, and innovation collide, we create opportunity from complexity. Our teams of interdisciplinary experts combine innovative thinking and breakthrough technologies to progress further, faster. Our clients adapt and transform, and together we achieve enduring results. We are over 4,000 strategists, innovators, designers, consultants, digital experts, scientists, engineers, and technologists. And we have deep expertise in consumer and manufacturing, defence and security, energy and utilities, financial services, government and public services, health and life sciences, and transport. Our teams operate globally from offices across the UK, Ireland, US, Nordics, and Netherlands. PA. Bringing Ingenuity to Life. We believe in the power of ingenuity to build a positive human future. We challenge where it matters and own the outcome. We combine strategic thinking, customer-centric service design, and agile engineering practices to accelerate innovation in a tech-driven world. Join our Digital & Data team working alongside product, design and a wide range of other experts and cross-disciplinary teams to bring ideas to life through innovative software solutions. Grow a flexible and unique career within a trust-based, inclusive environment that values excellence, innovation, and curiosity. You have the option to progress with us on a technical career track. No need to go onto the Partner career track if this doesn't align with what you want to do. Hybrid working - our approach is to be in the office or on client site minimum of 2 days per week. Work on a broad variety of projects and tech stacks for clients across seven sectors - no project is ever the same Join other experts within our supportive and collaborative tech community through knowledge-sharing and peer-level support, coaching and mentoring Deepen your expertise through our a culture of learning and growth - you'll have budget to take courses (technical and non-technical training), plus gain certifications While we advocate for using the right tech for the right task, you can expect to work with the following technologies to ensure scalable, high-performance applications: Architecture frameworks: TOGAF, Zachmann, MODAF Agile methodologies: SAFe, Scrum, Kanban Modeling tools: UML, ArchiMate, Ardoq What you can expect Create and assure key architecture artefacts (e.g., Key Design Decision, Technical Options Paper, High Level Design) Collaborate closely with Engineering teams, often taking a lead SME role to define vision and establish Architectural Guardrails. Support senior leaders in shaping their case for change, leading on cost estimation and detailed planning. Work to agile best practices and cross-functionally with multiple teams and stakeholders. You'll be using your technical skills to problem solve with our clients, as well as working on internal projects Hybrid working with the team on client site or in our office a minimum of two days per week. However, the actual time you spend and where you spend it will vary by role or assignment, including up to 5 days per week on a client site. An environment that deeply cares about its values Qualifications Essential requirements Even if you don't meet every requirement below, feel free to still apply as we are often hiring for similar roles which your background might be better suited to. Hands-on Software Engineering background with experience leading engineering teams to deliver applications and services. Clear understanding and practical application of architecture and delivery methodologies. Operate confidently across all architectural domains with a specialism in at least one: Business, Data, Application, Technology, and Security. Commitment to continuous improvement and professional development. You thrive in problem-solving and analytical thinking You enjoy collaborating with multiple stakeholders in a fast-paced environment Certifications in appropriate methodologies and cloud technologies are advantageous. We're technology agnostic, using the right tools for the job at hand, and you'll have access to our strong partnerships with AWS, Azure and GCP. We're interested to hear from Solution Architects with experience across the majority of leading vendors including Azure, AWS, Google Cloud Platform, Oracle, IBM, Salesforce and more. Additional information Quick video call with one of our Tech Recruiters - to discuss your application, the role and PA Round 1: Either a competency or technical interview (60 mins) Round 2: Either a competency or technical interview, whichever you didn't do at first round (60 mins) Final round : Meeting with a PA leader - a discussion around your client-centricity (45 mins) Life At PA encompasses our peoples' experience at PA. It's about how we enrich peoples' working lives by giving them access to unique people and growth opportunities and purpose led meaningful work. Our purpose guides how we work with our clients and our teams, and support our communities, to deliver insight and impact, solving the world's most complex challenges. We're focused on building a workplace that values human difference and diverse mindsets, and a culture of inclusion and equality that unlocks the potential in our people so everyone can be their best self. We are dedicated to supporting the physical, emotional, social and financial well-being of our people. Check out some of our extensive benefits: Health and lifestyle perks accompanying private healthcare for you and your family 25 days annual leave (plus a bonus half day on Christmas Eve) with the opportunity to buy 5 additional days Generous company pension scheme Opportunity to get involved with community and charity-based initiatives Annual performance-based bonus PA share ownership Tax efficient benefits (cycle to work, give as you earn) We're committed to advancing equality.We recruit, retain, reward and develop our people based solely on their abilities and contributions and without reference to their age, background, disability, genetic information, parental or family status, religion or belief, race, ethnicity, nationality, sex, sexual orientation, gender identity (or expression), political belief veteran status, or other by any other range of human difference brought about by identity and experience. We welcome applications from underrepresented groups. Adjustments or accommodations - Should you need any adjustments or accommodations to the recruitment process, at either application or interview, please contact us on
Aug 14, 2025
Full time
We believe in the power of ingenuity to build a positive human future. As strategies, technologies, and innovation collide, we create opportunity from complexity. Our teams of interdisciplinary experts combine innovative thinking and breakthrough technologies to progress further, faster. Our clients adapt and transform, and together we achieve enduring results. We are over 4,000 strategists, innovators, designers, consultants, digital experts, scientists, engineers, and technologists. And we have deep expertise in consumer and manufacturing, defence and security, energy and utilities, financial services, government and public services, health and life sciences, and transport. Our teams operate globally from offices across the UK, Ireland, US, Nordics, and Netherlands. PA. Bringing Ingenuity to Life. We believe in the power of ingenuity to build a positive human future. We challenge where it matters and own the outcome. We combine strategic thinking, customer-centric service design, and agile engineering practices to accelerate innovation in a tech-driven world. Join our Digital & Data team working alongside product, design and a wide range of other experts and cross-disciplinary teams to bring ideas to life through innovative software solutions. Grow a flexible and unique career within a trust-based, inclusive environment that values excellence, innovation, and curiosity. You have the option to progress with us on a technical career track. No need to go onto the Partner career track if this doesn't align with what you want to do. Hybrid working - our approach is to be in the office or on client site minimum of 2 days per week. Work on a broad variety of projects and tech stacks for clients across seven sectors - no project is ever the same Join other experts within our supportive and collaborative tech community through knowledge-sharing and peer-level support, coaching and mentoring Deepen your expertise through our a culture of learning and growth - you'll have budget to take courses (technical and non-technical training), plus gain certifications While we advocate for using the right tech for the right task, you can expect to work with the following technologies to ensure scalable, high-performance applications: Architecture frameworks: TOGAF, Zachmann, MODAF Agile methodologies: SAFe, Scrum, Kanban Modeling tools: UML, ArchiMate, Ardoq What you can expect Create and assure key architecture artefacts (e.g., Key Design Decision, Technical Options Paper, High Level Design) Collaborate closely with Engineering teams, often taking a lead SME role to define vision and establish Architectural Guardrails. Support senior leaders in shaping their case for change, leading on cost estimation and detailed planning. Work to agile best practices and cross-functionally with multiple teams and stakeholders. You'll be using your technical skills to problem solve with our clients, as well as working on internal projects Hybrid working with the team on client site or in our office a minimum of two days per week. However, the actual time you spend and where you spend it will vary by role or assignment, including up to 5 days per week on a client site. An environment that deeply cares about its values Qualifications Essential requirements Even if you don't meet every requirement below, feel free to still apply as we are often hiring for similar roles which your background might be better suited to. Hands-on Software Engineering background with experience leading engineering teams to deliver applications and services. Clear understanding and practical application of architecture and delivery methodologies. Operate confidently across all architectural domains with a specialism in at least one: Business, Data, Application, Technology, and Security. Commitment to continuous improvement and professional development. You thrive in problem-solving and analytical thinking You enjoy collaborating with multiple stakeholders in a fast-paced environment Certifications in appropriate methodologies and cloud technologies are advantageous. We're technology agnostic, using the right tools for the job at hand, and you'll have access to our strong partnerships with AWS, Azure and GCP. We're interested to hear from Solution Architects with experience across the majority of leading vendors including Azure, AWS, Google Cloud Platform, Oracle, IBM, Salesforce and more. Additional information Quick video call with one of our Tech Recruiters - to discuss your application, the role and PA Round 1: Either a competency or technical interview (60 mins) Round 2: Either a competency or technical interview, whichever you didn't do at first round (60 mins) Final round : Meeting with a PA leader - a discussion around your client-centricity (45 mins) Life At PA encompasses our peoples' experience at PA. It's about how we enrich peoples' working lives by giving them access to unique people and growth opportunities and purpose led meaningful work. Our purpose guides how we work with our clients and our teams, and support our communities, to deliver insight and impact, solving the world's most complex challenges. We're focused on building a workplace that values human difference and diverse mindsets, and a culture of inclusion and equality that unlocks the potential in our people so everyone can be their best self. We are dedicated to supporting the physical, emotional, social and financial well-being of our people. Check out some of our extensive benefits: Health and lifestyle perks accompanying private healthcare for you and your family 25 days annual leave (plus a bonus half day on Christmas Eve) with the opportunity to buy 5 additional days Generous company pension scheme Opportunity to get involved with community and charity-based initiatives Annual performance-based bonus PA share ownership Tax efficient benefits (cycle to work, give as you earn) We're committed to advancing equality.We recruit, retain, reward and develop our people based solely on their abilities and contributions and without reference to their age, background, disability, genetic information, parental or family status, religion or belief, race, ethnicity, nationality, sex, sexual orientation, gender identity (or expression), political belief veteran status, or other by any other range of human difference brought about by identity and experience. We welcome applications from underrepresented groups. Adjustments or accommodations - Should you need any adjustments or accommodations to the recruitment process, at either application or interview, please contact us on
14737 Contract £28 - £33 Per Hour Hybrid London - United Kingdom Updated on: 31-07-2025 We are recruiting a Senior Scientist to join a leading Pharmaceutical company in the Berkshire area for an initial 12 months. As the Senior Scientist, you will be offered the chance to work alongside a team of 60 experienced scientists dedicated to the characterisation of molecules and materials, and you will be focused on Biological Characterisation Projects. KEY DUTIES AND RESPONSIBILITIES: Your duties as the Senior Scientist / Biological Characterisation Lead will be varied however the key duties and responsibilities are as follows: 1. As the Senior Scientist, you will design and lead characterisation studies, including CQA (Critical Quality Attribute) assessments, and manage documentation such as protocols, reports, and risk assessments. 2. As the Senior Scientist, you will collaborate with various scientific teams, including formulation, analytical method development, and regulatory colleagues, to ensure comprehensive project support. 3. As the Senior Scientist, you will present data and findings to wider project teams, ensuring clear communication and effective project management. 4. As the Senior Scientist, you will support early phase projects preparing for INDs, with potential involvement in later phase projects. ROLE REQUIREMENTS: To be successful in your application to this exciting role as the Senior Scientist / Biological Characterisation Project Lead we are looking to identify the following on your profile and past history: 1. Relevant degree in a scientific discipline. 2. Proven industry experience in the characterisation of biologics. It would be advantage to have experience with Mass Spectrometry (LCMS), NMR (Nuclear Magnetic Resonance) and Antibodies 3. A working knowledge and practical experience with project management in a scientific setting. Key Words: Biological Characterisation / Project Lead / Senior Scientist / Mass Spectrometry / Protein Chemistry / CQA Assessments / IND Preparation / Life Sciences / Analytical Method Development / Regulatory Compliance / Scientific Collaboration / NMR / Nuclear Magnetic Resonance / Antibody Development / Antibody Characterisation / Antibodies / LCMS / Mass Spec / Senior Scientist / Research Scientist / R&D Scientist Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the Life Science sectors, combining recruitment expertise with scientific knowledge to help you advance your career. Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career. Your next opportunity is just a click away!
Aug 14, 2025
Full time
14737 Contract £28 - £33 Per Hour Hybrid London - United Kingdom Updated on: 31-07-2025 We are recruiting a Senior Scientist to join a leading Pharmaceutical company in the Berkshire area for an initial 12 months. As the Senior Scientist, you will be offered the chance to work alongside a team of 60 experienced scientists dedicated to the characterisation of molecules and materials, and you will be focused on Biological Characterisation Projects. KEY DUTIES AND RESPONSIBILITIES: Your duties as the Senior Scientist / Biological Characterisation Lead will be varied however the key duties and responsibilities are as follows: 1. As the Senior Scientist, you will design and lead characterisation studies, including CQA (Critical Quality Attribute) assessments, and manage documentation such as protocols, reports, and risk assessments. 2. As the Senior Scientist, you will collaborate with various scientific teams, including formulation, analytical method development, and regulatory colleagues, to ensure comprehensive project support. 3. As the Senior Scientist, you will present data and findings to wider project teams, ensuring clear communication and effective project management. 4. As the Senior Scientist, you will support early phase projects preparing for INDs, with potential involvement in later phase projects. ROLE REQUIREMENTS: To be successful in your application to this exciting role as the Senior Scientist / Biological Characterisation Project Lead we are looking to identify the following on your profile and past history: 1. Relevant degree in a scientific discipline. 2. Proven industry experience in the characterisation of biologics. It would be advantage to have experience with Mass Spectrometry (LCMS), NMR (Nuclear Magnetic Resonance) and Antibodies 3. A working knowledge and practical experience with project management in a scientific setting. Key Words: Biological Characterisation / Project Lead / Senior Scientist / Mass Spectrometry / Protein Chemistry / CQA Assessments / IND Preparation / Life Sciences / Analytical Method Development / Regulatory Compliance / Scientific Collaboration / NMR / Nuclear Magnetic Resonance / Antibody Development / Antibody Characterisation / Antibodies / LCMS / Mass Spec / Senior Scientist / Research Scientist / R&D Scientist Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the Life Science sectors, combining recruitment expertise with scientific knowledge to help you advance your career. Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career. Your next opportunity is just a click away!
Senior Scientist, Quantitative Biosciences (1-Year Fixed-Term Contract) page is loaded Senior Scientist, Quantitative Biosciences (1-Year Fixed-Term Contract) Apply remote type Not Applicable locations GBR - London - London (Francis Crick Institute) time type Full time posted on Posted Yesterday time left to apply End Date: August 15, 2025 (14 days left to apply) job requisition id R359526 Job Description Our company has a rapidly growing, interdisciplinary team of scientists in London and exciting plans to expand our London presence. This will initially be at the Francis Crick Institute as part of our 'Skylab' expansion, and from 2027 in our new 'state of art' and fully integrated Research and Discovery Centre at the hub of London's knowledge Quarter. This new building will be home to approximately 180 scientists alongside other colleagues in discovery research, clinical, regulatory and business roles, including marketing, finance and administration. We have an exciting Senior Scientist opportunity for a Biochemist/pharmacologist to join our team at the Francis Crick Institute in London on a 1-year fixed term contract. Working collaboratively with our London discovery teams you will apply your skills in biochemical/biophysical assay development, data analysis, laboratory automation and detection technologies to advance therapeutic programs across the Immunology and Neuroscience therapy areas. If you are lab-focused, scientifically curious and looking to develop your skills, we'd love for you to be part of our diverse and passionate team. In this role you will: Design and execute quantitative biochemical and biophysical assays to identify, characterize, and optimize candidates for therapeutic programs aimed at Immunology/Neuroscience related diseases. Conduct molecular mechanism of action studies to understand compound efficacy and specificity, as well as the downstream impact to biology. Apply automation to functional assays to deliver impactful data at scale. Collaborate on new technology initiatives to evaluate, implement and build internal capabilities. Collaborate with our London-based disease area and genome sciences colleagues as needed to identify our next generation of drug targets. Conceptualize and enact innovative approaches to solve program objectives and issues. Manage project-specific milestones and timelines. Interpret data and communicate science and strategy to stakeholders and management. Take on increasing responsibility within the Quantitative Biosciences group and on project teams as your skills develop. What you will need: Educated to Ph.D, or BSc/MSc level with experience in biotech/pharma; experience in Neuroscience and/or Immunology would be useful but not essential. Proven ability to independently design, implement and interpret complex biochemical/biophysical assays using fluorescence and label-free technologies and associated analytical software solutions. This may include proficiency in techniques such as SPR, thermal shift, FP, TR-FRET and luminescence & absorbance-based techniques. Practical experience in the characterisation of isolated targets, which may include but not be limited to catalytic mechanism determination, compound-inhibitor mechanism of action studies and quantitative measurement of the kinetics of drug-target interactions. An ability to propose new, innovative approaches and experimental designs as needed. Experience with medium to high throughput assay-related data analysis and an appreciation for the related quantitative and statistical concepts. A flexible and collaborative approach to working across teams, projects and departments. Effective written and oral communication skills. The ability to adapt to changing priorities with a passion for innovation and problem-solving. We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another's thinking and approach problems collectively. We are an equal opportunity employer, committed to fostering an inclusive and diverse workplace. The closing date for applications will be 11:59pm on Thursday 14th August. Current Employees apply HERE Current Contingent Workers apply HERE Search Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. Employee Status: Project Temps (Fixed Term) Relocation: VISA Sponsorship: Travel Requirements: Flexible Work Arrangements: Not Applicable Shift: Valid Driving License: Hazardous Material(s): Required Skills: Adaptability, Adaptability, Assay, Assay Development, Biochemical Assays, Cell-Based Assays, Cell Culture Techniques, Clinical Immunology, Communication, Data Analysis, Detail-Oriented, Drug Target Identification, Flow Cytometry, Fluorescence, High Content Screening, Immunoassays, Immunology, Laboratory Automation, Molecular Biology, Neuroanatomy, Oral Communications, Personal Initiative, Project Management, Protein Purifications, Quantitative Assay + 3 more Preferred Skills: Job Posting End Date: 08/15/2025 A job posting is effective until 11:59:59PM on the day BEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date. Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where we have codified our legacy for over a century. Our success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.
Aug 14, 2025
Full time
Senior Scientist, Quantitative Biosciences (1-Year Fixed-Term Contract) page is loaded Senior Scientist, Quantitative Biosciences (1-Year Fixed-Term Contract) Apply remote type Not Applicable locations GBR - London - London (Francis Crick Institute) time type Full time posted on Posted Yesterday time left to apply End Date: August 15, 2025 (14 days left to apply) job requisition id R359526 Job Description Our company has a rapidly growing, interdisciplinary team of scientists in London and exciting plans to expand our London presence. This will initially be at the Francis Crick Institute as part of our 'Skylab' expansion, and from 2027 in our new 'state of art' and fully integrated Research and Discovery Centre at the hub of London's knowledge Quarter. This new building will be home to approximately 180 scientists alongside other colleagues in discovery research, clinical, regulatory and business roles, including marketing, finance and administration. We have an exciting Senior Scientist opportunity for a Biochemist/pharmacologist to join our team at the Francis Crick Institute in London on a 1-year fixed term contract. Working collaboratively with our London discovery teams you will apply your skills in biochemical/biophysical assay development, data analysis, laboratory automation and detection technologies to advance therapeutic programs across the Immunology and Neuroscience therapy areas. If you are lab-focused, scientifically curious and looking to develop your skills, we'd love for you to be part of our diverse and passionate team. In this role you will: Design and execute quantitative biochemical and biophysical assays to identify, characterize, and optimize candidates for therapeutic programs aimed at Immunology/Neuroscience related diseases. Conduct molecular mechanism of action studies to understand compound efficacy and specificity, as well as the downstream impact to biology. Apply automation to functional assays to deliver impactful data at scale. Collaborate on new technology initiatives to evaluate, implement and build internal capabilities. Collaborate with our London-based disease area and genome sciences colleagues as needed to identify our next generation of drug targets. Conceptualize and enact innovative approaches to solve program objectives and issues. Manage project-specific milestones and timelines. Interpret data and communicate science and strategy to stakeholders and management. Take on increasing responsibility within the Quantitative Biosciences group and on project teams as your skills develop. What you will need: Educated to Ph.D, or BSc/MSc level with experience in biotech/pharma; experience in Neuroscience and/or Immunology would be useful but not essential. Proven ability to independently design, implement and interpret complex biochemical/biophysical assays using fluorescence and label-free technologies and associated analytical software solutions. This may include proficiency in techniques such as SPR, thermal shift, FP, TR-FRET and luminescence & absorbance-based techniques. Practical experience in the characterisation of isolated targets, which may include but not be limited to catalytic mechanism determination, compound-inhibitor mechanism of action studies and quantitative measurement of the kinetics of drug-target interactions. An ability to propose new, innovative approaches and experimental designs as needed. Experience with medium to high throughput assay-related data analysis and an appreciation for the related quantitative and statistical concepts. A flexible and collaborative approach to working across teams, projects and departments. Effective written and oral communication skills. The ability to adapt to changing priorities with a passion for innovation and problem-solving. We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another's thinking and approach problems collectively. We are an equal opportunity employer, committed to fostering an inclusive and diverse workplace. The closing date for applications will be 11:59pm on Thursday 14th August. Current Employees apply HERE Current Contingent Workers apply HERE Search Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. Employee Status: Project Temps (Fixed Term) Relocation: VISA Sponsorship: Travel Requirements: Flexible Work Arrangements: Not Applicable Shift: Valid Driving License: Hazardous Material(s): Required Skills: Adaptability, Adaptability, Assay, Assay Development, Biochemical Assays, Cell-Based Assays, Cell Culture Techniques, Clinical Immunology, Communication, Data Analysis, Detail-Oriented, Drug Target Identification, Flow Cytometry, Fluorescence, High Content Screening, Immunoassays, Immunology, Laboratory Automation, Molecular Biology, Neuroanatomy, Oral Communications, Personal Initiative, Project Management, Protein Purifications, Quantitative Assay + 3 more Preferred Skills: Job Posting End Date: 08/15/2025 A job posting is effective until 11:59:59PM on the day BEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date. Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where we have codified our legacy for over a century. Our success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.
NLP / LLM Scientist - Applied AI ML Lead - Machine Learning Centre of Excellence The Machine Learning Center of Excellence invites the successful candidate to apply sophisticated machine learning methods to a wide variety of complex tasks including natural language processing, speech analytics, time series, reinforcement learning and recommendation systems. The candidate must excel in working in a highly collaborative environment together with the business, technologists and control partners to deploy solutions into production. The candidate must also have a strong passion for machine learning and invest independent time towards learning, researching and experimenting with new innovations in the field. The candidate must have solid expertise in Deep Learning with hands-on implementation experience and possess strong analytical thinking, a deep desire to learn and be highly motivated. Job Responsibilities • Research and explore new machine learning methods through independent study, attending industry-leading conferences, experimentation and participating in our knowledge sharing community • Develop state-of-the art machine learning models to solve real-world problems and apply it to tasks such as NLP, speech recognition and analytics, time-series predictions or recommendation systems • Collaborate with multiple partner teams such as Business, Technology, Product Management, Legal, Compliance, Strategy and Business Management to deploy solutions into production • Drive Firm wide initiatives by developing large-scale frameworks to accelerate the application of machine learning models across different areas of the business Required qualifications, capabilities, and skills • Solid background in NLP or speech recognition and analytics, personalization/recommendation and hands-on experience and solid understanding of machine learning and deep learning methods • PhD in a quantitative discipline, e.g. Computer Science, Electrical Engineering, Mathematics, Operations Research, Optimization, or Data Science with reasonable industry experience, or an MS with significant industry or research experience in the field • Extensive experience with machine learning and deep learning toolkits (e.g.: TensorFlow, PyTorch, NumPy, Scikit-Learn, Pandas) • Ability to design experiments and training frameworks, and to outline and evaluate intrinsic and extrinsic metrics for model performance aligned with business goals • Experience with big data and scalable model training and solid written and spoken communication to effectively communicate technical concepts and results to both technical and business audiences. • Scientific thinking with the ability to invent and to work both independently and in highly collaborative team environments • Solid written and spoken communication to effectively communicate technical concepts and results to both technical and business audiences. Curious, hardworking and detail-oriented, and motivated by complex analytical problems Preferred qualifications, capabilities, and skills • Strong background in Mathematics and Statistics and familiarity with the financial services industries and continuous integration models and unit test development • Knowledge in search/ranking, Reinforcement Learning or Meta Learning • Experience with A/B experimentation and data/metric-driven product development, cloud-native deployment in a large scale distributed environment and ability to develop and debug production-quality code • Published research in areas of Machine Learning, Deep Learning or Reinforcement Learning at a major conference or journal About MLCOE The Machine Learning Center of Excellence (MCLOE) team partners across the firm to create and share Machine Learning Solutions for our most challenging business problems. In this role you will work and collaborate with a team comprised of a multi-disciplinary community of experts focused exclusively on Machine Learning. On this team you will work with cutting-edge techniques in disciplines such as Deep Learning and Reinforcement Learning For more information about the MLCOE, please visit To learn about how we're using AI/ML to drive transformational change, please read this blog: The Chief Data & Analytics Office (CDAO) at JPMorgan Chase is responsible for accelerating the firm's data and analytics journey. This includes ensuring the quality, integrity, and security of the company's data, as well as leveraging this data to generate insights and drive decision-making. The CDAO is also responsible for developing and implementing solutions that support the firm's commercial goals by harnessing artificial intelligence and machine learning technologies to develop new products, improve productivity, and enhance risk management effectively and responsibly. Company: Chase- Candidate Experience page Qualifications: Language requirements: Specific requirements: Educational level: Level of experience (years): Senior (5+ years of experience) Tagged as: Big Data , Industry , Natural Language Processing , NLP , Speech Recognition , United Kingdom
Aug 14, 2025
Full time
NLP / LLM Scientist - Applied AI ML Lead - Machine Learning Centre of Excellence The Machine Learning Center of Excellence invites the successful candidate to apply sophisticated machine learning methods to a wide variety of complex tasks including natural language processing, speech analytics, time series, reinforcement learning and recommendation systems. The candidate must excel in working in a highly collaborative environment together with the business, technologists and control partners to deploy solutions into production. The candidate must also have a strong passion for machine learning and invest independent time towards learning, researching and experimenting with new innovations in the field. The candidate must have solid expertise in Deep Learning with hands-on implementation experience and possess strong analytical thinking, a deep desire to learn and be highly motivated. Job Responsibilities • Research and explore new machine learning methods through independent study, attending industry-leading conferences, experimentation and participating in our knowledge sharing community • Develop state-of-the art machine learning models to solve real-world problems and apply it to tasks such as NLP, speech recognition and analytics, time-series predictions or recommendation systems • Collaborate with multiple partner teams such as Business, Technology, Product Management, Legal, Compliance, Strategy and Business Management to deploy solutions into production • Drive Firm wide initiatives by developing large-scale frameworks to accelerate the application of machine learning models across different areas of the business Required qualifications, capabilities, and skills • Solid background in NLP or speech recognition and analytics, personalization/recommendation and hands-on experience and solid understanding of machine learning and deep learning methods • PhD in a quantitative discipline, e.g. Computer Science, Electrical Engineering, Mathematics, Operations Research, Optimization, or Data Science with reasonable industry experience, or an MS with significant industry or research experience in the field • Extensive experience with machine learning and deep learning toolkits (e.g.: TensorFlow, PyTorch, NumPy, Scikit-Learn, Pandas) • Ability to design experiments and training frameworks, and to outline and evaluate intrinsic and extrinsic metrics for model performance aligned with business goals • Experience with big data and scalable model training and solid written and spoken communication to effectively communicate technical concepts and results to both technical and business audiences. • Scientific thinking with the ability to invent and to work both independently and in highly collaborative team environments • Solid written and spoken communication to effectively communicate technical concepts and results to both technical and business audiences. Curious, hardworking and detail-oriented, and motivated by complex analytical problems Preferred qualifications, capabilities, and skills • Strong background in Mathematics and Statistics and familiarity with the financial services industries and continuous integration models and unit test development • Knowledge in search/ranking, Reinforcement Learning or Meta Learning • Experience with A/B experimentation and data/metric-driven product development, cloud-native deployment in a large scale distributed environment and ability to develop and debug production-quality code • Published research in areas of Machine Learning, Deep Learning or Reinforcement Learning at a major conference or journal About MLCOE The Machine Learning Center of Excellence (MCLOE) team partners across the firm to create and share Machine Learning Solutions for our most challenging business problems. In this role you will work and collaborate with a team comprised of a multi-disciplinary community of experts focused exclusively on Machine Learning. On this team you will work with cutting-edge techniques in disciplines such as Deep Learning and Reinforcement Learning For more information about the MLCOE, please visit To learn about how we're using AI/ML to drive transformational change, please read this blog: The Chief Data & Analytics Office (CDAO) at JPMorgan Chase is responsible for accelerating the firm's data and analytics journey. This includes ensuring the quality, integrity, and security of the company's data, as well as leveraging this data to generate insights and drive decision-making. The CDAO is also responsible for developing and implementing solutions that support the firm's commercial goals by harnessing artificial intelligence and machine learning technologies to develop new products, improve productivity, and enhance risk management effectively and responsibly. Company: Chase- Candidate Experience page Qualifications: Language requirements: Specific requirements: Educational level: Level of experience (years): Senior (5+ years of experience) Tagged as: Big Data , Industry , Natural Language Processing , NLP , Speech Recognition , United Kingdom
Are you passionate about improving health and improving lives? Do you thrive in a dynamic, collaborative setting where your expertise drives innovation and regulatory excellence? Are you a seasoned ecotoxicology expert ready to lead scientific strategy and shape the future of regulatory science? We are currently looking for a visionary Principal Scientist to join our Ecotoxicology team based in Shardlow, Derbyshire , where you will be at the forefront of ecotoxicological testing, shaping strategies, mentoring teams, and delivering high-impact solutions. Your work will influence regulatory decisions and contribute to environmental sustainability. As a senior scientific leader, you will oversee and advance our ecotoxicology initiatives. You'll be the go-to expert for technical excellence, guideline compliance and scientific innovation. Ensuring our services meet the highest standards and support long-term strategic growth. Job Responsibilities will include: Lead scientific development and excellence in ecotoxicology Deliver robust regulatory science aligned with global standards Provide expert consultation and mentorship to scientific teams Interpret complex data and ensure high-quality reporting Collaborate with analytical and operational leaders to optimize outcomes Evaluate and implement new technologies and assay capabilities Represent the organization in client meetings, conferences, and scientific forums Support business development through technical consultation and client engagement What Labcorp can offer you: Competitive salary and a comprehensive benefits package, including health coverage and contributory pension Clearly defined career development opportunities An opportunity to work in a rapidly expanding department A chance to effect positive change within a global organization Skills and experience Extensive experience in ecotoxicology or a related scientific field Proven expertise in regulatory ecotoxicology and scientific reporting Experience with OECD guideline-based method development and validation Strong background in research, data interpretation, and technical process development Excellent communication and presentation skills Proficiency in laboratory systems, Microsoft applications, and statistics Sponsorship and relocation assistance may be available for this role as will a degree of flexible working. Labcorp is proud to be an Equal Opportunity Employer: Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. A dditionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. We encourage all to apply If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at Labcorp Accessibility. Formore information about how we collect and store your personal data, please see our Privacy Statement .
Aug 14, 2025
Full time
Are you passionate about improving health and improving lives? Do you thrive in a dynamic, collaborative setting where your expertise drives innovation and regulatory excellence? Are you a seasoned ecotoxicology expert ready to lead scientific strategy and shape the future of regulatory science? We are currently looking for a visionary Principal Scientist to join our Ecotoxicology team based in Shardlow, Derbyshire , where you will be at the forefront of ecotoxicological testing, shaping strategies, mentoring teams, and delivering high-impact solutions. Your work will influence regulatory decisions and contribute to environmental sustainability. As a senior scientific leader, you will oversee and advance our ecotoxicology initiatives. You'll be the go-to expert for technical excellence, guideline compliance and scientific innovation. Ensuring our services meet the highest standards and support long-term strategic growth. Job Responsibilities will include: Lead scientific development and excellence in ecotoxicology Deliver robust regulatory science aligned with global standards Provide expert consultation and mentorship to scientific teams Interpret complex data and ensure high-quality reporting Collaborate with analytical and operational leaders to optimize outcomes Evaluate and implement new technologies and assay capabilities Represent the organization in client meetings, conferences, and scientific forums Support business development through technical consultation and client engagement What Labcorp can offer you: Competitive salary and a comprehensive benefits package, including health coverage and contributory pension Clearly defined career development opportunities An opportunity to work in a rapidly expanding department A chance to effect positive change within a global organization Skills and experience Extensive experience in ecotoxicology or a related scientific field Proven expertise in regulatory ecotoxicology and scientific reporting Experience with OECD guideline-based method development and validation Strong background in research, data interpretation, and technical process development Excellent communication and presentation skills Proficiency in laboratory systems, Microsoft applications, and statistics Sponsorship and relocation assistance may be available for this role as will a degree of flexible working. Labcorp is proud to be an Equal Opportunity Employer: Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. A dditionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. We encourage all to apply If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at Labcorp Accessibility. Formore information about how we collect and store your personal data, please see our Privacy Statement .
Senior Scientist CRISPR R&D - Functional Genomics London About Relation Relation is an end-to-end biotech developing transformational medicines, with technology at our core. Our ambition is to understand human biology in unprecedented ways, discovering therapies to treat some of life's most devastating diseases. We leverage single-cell multi-omics directly from patient tissue, functional assays, and machine learning to drive disease understanding, from cause to cure. This year, we've embarked on an exciting double collaboration with GSK to tackle fibrosis and osteoarthritis, alongside advancing our own internal osteoporosis programme. By combining our cutting-edge ML capabilities with their deep expertise in drug discovery, this partnership underscores our commitment to pioneering science and delivering impactful therapies to patients. We are rapidly scaling our technology and discovery teams, offering a unique opportunity to join one of the most innovative TechBio companies. Be part of our dynamic, interdisciplinary teams, collaborating closely to redefine the boundaries of possibility in drug discovery. Our state-of-the-art wet and dry laboratories, located in the heart of London, provide an exceptional environment to foster interdisciplinarity and turn groundbreaking ideas into positive impact for patients. We are committed to building diverse and inclusive teams. Relation is an equal opportunities employer and does not discriminate on the grounds of gender, sexual orientation, marital or civil partner status, gender reassignment, race, colour, nationality, ethnic or national origin, religion or belief, disability, or age. We cultivate innovation through collaboration, empowering every team member to do their best work and develop to their highest potential. By joining Relation, you will be part of an exceptionally talented team, with extraordinary leverage to advance the field of drug discovery. Your work will shape our culture, strategic direction, and, most importantly, impact patients' lives. The Opportunity Relation has an excellent opportunity for a Senior Scientist to join an interdisciplinary, highly collaborative team of experimental and computational drug discovery researchers in our newly built, state-of-the-art functional genomics lab in London. Large-scale genetic studies, including genome-wide association studies (GWAS), have identified thousands of variants and loci associated with complex diseases. However, the vast majority of these loci lie in non-coding regions of the genome with unknown functions, making it challenging to draw disease insights. At Relation, we generate proprietary large-scale datasets to accelerate the prediction of disease genes from these loci using state-of-the-art machine learning methods. We identify the key effector genes, cells, and pathways involved in disease pathophysiology to build disease-relevant assays and validate ML platform predictions, identifying candidate targets for further validation. We have an exciting opportunity for a talented Senior Scientist to contribute intellectually and experimentally to this endeavour. By joining Relation, you will be part of an exceptionally talented team, gain exposure to a broad range of skills beyond your area of expertise, help shape our culture and strategic direction, and ultimately, make a positive impact on patients' lives. As the company grows rapidly, there may be opportunities to supervise a small team. Professionally, you have A PhD with at least 3 years of experience and an outstanding track record in academia, biotech or pharma. At least 2 years' hands-on experience with all aspects of CRISPR technology (including CRISPRn, CRISPRi, CRISPRa, Cas9 and derivatives, Cas13). Extensive experience with mammalian cell transduction using lentiviral particles, cell transfection, lipofection, and nucleofection. Extensive experience with molecular cloning and mammalian cell engineering (TOPO, Gateway, Gibson, Golden Gate, reporter systems). Experience with flow cytometry and cell sorting. Broad experience with standard molecular biology techniques. A proven ability to deliver to tight timelines. Desirable knowledge or experiences Experience with siRNA, ASO, and other interventions for protein function modulation. Experience with assay development, screening, and liquid handling. Experience of interdisciplinary team-working, especially with computational scientists. Personally, you have A willingness to operate within start-up environments, including delivering to tight timelines, the ability to react to changing priorities or plans, and to help with laboratory operations. Excellent attention to detail, analytical, and critical thinking skills An ability to build effective working relationships with proven team-working skills An ability to communicate effectively with scientists from multiple disciplines An inquisitive nature, are self-motivated, and eager to learn A desire to work within a fast-paced, data science-first environment. Join Us This is an exciting opportunity to be part of a company that is redefining how we understand genetics and disease risk. Your contributions will directly impact the development of transformative medicines for patients. Together, we're not just conducting research-we're setting new standards in machine learning and genetics. The patient is waiting. Relation is a committed equal opportunities employer. Recruitment Agencies Please note that Relation does not accept unsolicited resumes from agencies. Resumes should not be forwarded to our job aliases or employees. Relation will not be liable for any fees associated with unsolicited CVs.
Aug 14, 2025
Full time
Senior Scientist CRISPR R&D - Functional Genomics London About Relation Relation is an end-to-end biotech developing transformational medicines, with technology at our core. Our ambition is to understand human biology in unprecedented ways, discovering therapies to treat some of life's most devastating diseases. We leverage single-cell multi-omics directly from patient tissue, functional assays, and machine learning to drive disease understanding, from cause to cure. This year, we've embarked on an exciting double collaboration with GSK to tackle fibrosis and osteoarthritis, alongside advancing our own internal osteoporosis programme. By combining our cutting-edge ML capabilities with their deep expertise in drug discovery, this partnership underscores our commitment to pioneering science and delivering impactful therapies to patients. We are rapidly scaling our technology and discovery teams, offering a unique opportunity to join one of the most innovative TechBio companies. Be part of our dynamic, interdisciplinary teams, collaborating closely to redefine the boundaries of possibility in drug discovery. Our state-of-the-art wet and dry laboratories, located in the heart of London, provide an exceptional environment to foster interdisciplinarity and turn groundbreaking ideas into positive impact for patients. We are committed to building diverse and inclusive teams. Relation is an equal opportunities employer and does not discriminate on the grounds of gender, sexual orientation, marital or civil partner status, gender reassignment, race, colour, nationality, ethnic or national origin, religion or belief, disability, or age. We cultivate innovation through collaboration, empowering every team member to do their best work and develop to their highest potential. By joining Relation, you will be part of an exceptionally talented team, with extraordinary leverage to advance the field of drug discovery. Your work will shape our culture, strategic direction, and, most importantly, impact patients' lives. The Opportunity Relation has an excellent opportunity for a Senior Scientist to join an interdisciplinary, highly collaborative team of experimental and computational drug discovery researchers in our newly built, state-of-the-art functional genomics lab in London. Large-scale genetic studies, including genome-wide association studies (GWAS), have identified thousands of variants and loci associated with complex diseases. However, the vast majority of these loci lie in non-coding regions of the genome with unknown functions, making it challenging to draw disease insights. At Relation, we generate proprietary large-scale datasets to accelerate the prediction of disease genes from these loci using state-of-the-art machine learning methods. We identify the key effector genes, cells, and pathways involved in disease pathophysiology to build disease-relevant assays and validate ML platform predictions, identifying candidate targets for further validation. We have an exciting opportunity for a talented Senior Scientist to contribute intellectually and experimentally to this endeavour. By joining Relation, you will be part of an exceptionally talented team, gain exposure to a broad range of skills beyond your area of expertise, help shape our culture and strategic direction, and ultimately, make a positive impact on patients' lives. As the company grows rapidly, there may be opportunities to supervise a small team. Professionally, you have A PhD with at least 3 years of experience and an outstanding track record in academia, biotech or pharma. At least 2 years' hands-on experience with all aspects of CRISPR technology (including CRISPRn, CRISPRi, CRISPRa, Cas9 and derivatives, Cas13). Extensive experience with mammalian cell transduction using lentiviral particles, cell transfection, lipofection, and nucleofection. Extensive experience with molecular cloning and mammalian cell engineering (TOPO, Gateway, Gibson, Golden Gate, reporter systems). Experience with flow cytometry and cell sorting. Broad experience with standard molecular biology techniques. A proven ability to deliver to tight timelines. Desirable knowledge or experiences Experience with siRNA, ASO, and other interventions for protein function modulation. Experience with assay development, screening, and liquid handling. Experience of interdisciplinary team-working, especially with computational scientists. Personally, you have A willingness to operate within start-up environments, including delivering to tight timelines, the ability to react to changing priorities or plans, and to help with laboratory operations. Excellent attention to detail, analytical, and critical thinking skills An ability to build effective working relationships with proven team-working skills An ability to communicate effectively with scientists from multiple disciplines An inquisitive nature, are self-motivated, and eager to learn A desire to work within a fast-paced, data science-first environment. Join Us This is an exciting opportunity to be part of a company that is redefining how we understand genetics and disease risk. Your contributions will directly impact the development of transformative medicines for patients. Together, we're not just conducting research-we're setting new standards in machine learning and genetics. The patient is waiting. Relation is a committed equal opportunities employer. Recruitment Agencies Please note that Relation does not accept unsolicited resumes from agencies. Resumes should not be forwarded to our job aliases or employees. Relation will not be liable for any fees associated with unsolicited CVs.
Are you a data visionary? Don't miss this opportunity to make a significant impact. Unlock the power of your data. Our client is seeking a highly skilled senior data science consultant to join their team. This is an exciting opportunity to work on challenging projects and drive business growth through data-driven insights. You'll be instrumental in driving data-driven solutions for their clients across various industries. Why This Role: Work on exciting projects: Be part of shaping the future of business and technology. Continuous learning: Access to cutting-edge training and development opportunities. Flexible work: Enjoy a balanced work-life with flexible work arrangements. Make a difference: Contribute to projects with a positive social impact. What You'll Do: Spearhead and deliver high-impact data science projects from conception to deployment, driving business value through data-driven insights. Develop and implement advanced data science models and algorithms to extract actionable insights from complex datasets. Master and apply cutting-edge AI and machine learning techniques to solve complex business challenges. Collaborate effectively with cross-functional teams to create innovative data solutions and drive business growth. Mentor and develop junior data scientists to build a high-performing data team and foster a data-driven culture. What You'll Need: Proven expertise in data science with a focus on delivering business value. With a preference for experience in a consulting role. Strong foundation in statistical modelling, machine learning, and data mining. Proficiency in Python, R, or similar programming languages. Experience with cloud platforms (AWS, GCP, Azure) is a plus. A passion for solving complex problems and a desire to make a lasting impact. Please note - this client is unable to offer sponsorship. Company: Graduate Recruitment Bureau (Hiring for client) Jobs related to Senior Consultant - Data Science: Elevate Your Data Strategy Our client, a global leader in the technology and consulting industry, is view job Shape the Future with Data A leading global technology and consulting firm is seeking a talented view job The Company An boutique firm who provides analytically-driven consumer insight services to a broad spectrum of view job
Aug 14, 2025
Full time
Are you a data visionary? Don't miss this opportunity to make a significant impact. Unlock the power of your data. Our client is seeking a highly skilled senior data science consultant to join their team. This is an exciting opportunity to work on challenging projects and drive business growth through data-driven insights. You'll be instrumental in driving data-driven solutions for their clients across various industries. Why This Role: Work on exciting projects: Be part of shaping the future of business and technology. Continuous learning: Access to cutting-edge training and development opportunities. Flexible work: Enjoy a balanced work-life with flexible work arrangements. Make a difference: Contribute to projects with a positive social impact. What You'll Do: Spearhead and deliver high-impact data science projects from conception to deployment, driving business value through data-driven insights. Develop and implement advanced data science models and algorithms to extract actionable insights from complex datasets. Master and apply cutting-edge AI and machine learning techniques to solve complex business challenges. Collaborate effectively with cross-functional teams to create innovative data solutions and drive business growth. Mentor and develop junior data scientists to build a high-performing data team and foster a data-driven culture. What You'll Need: Proven expertise in data science with a focus on delivering business value. With a preference for experience in a consulting role. Strong foundation in statistical modelling, machine learning, and data mining. Proficiency in Python, R, or similar programming languages. Experience with cloud platforms (AWS, GCP, Azure) is a plus. A passion for solving complex problems and a desire to make a lasting impact. Please note - this client is unable to offer sponsorship. Company: Graduate Recruitment Bureau (Hiring for client) Jobs related to Senior Consultant - Data Science: Elevate Your Data Strategy Our client, a global leader in the technology and consulting industry, is view job Shape the Future with Data A leading global technology and consulting firm is seeking a talented view job The Company An boutique firm who provides analytically-driven consumer insight services to a broad spectrum of view job
Exciting Opportunity: Join a rapidly growing Environmental Management and Assessment Team! Are you ready to take your career to new heights? My client's Environmental Management and Assessment Team is expanding, and hence on the lookout for passionate individuals at Principal and Senior levels to join their team across multiple locations in the UK. From Exeter to London, Luton to Birmingham, Wakefield to Manchester, this is your chance to be part of a dynamic team making a real difference. As a key member of the team, you'll have the opportunity to work on exciting projects spanning various sectors. From coordinating Environmental Impact Assessments to preparing Environmental Statements and Risk Assessments, you'll play a crucial role in delivering objective-led solutions that drive our business forward. Location Across the UK - Exeter, London, Luton, Birmingham, Wakefield, Manchester Responsibilities & Tasks Lead the coordination of Environmental Impact Assessments, ensuring high standards of safety, quality, and environmental responsibility. Prepare Environmental Statements, Management Plans, and Risk Assessments, demonstrating your expertise in environmental science and legislation. Collaborate with internal teams and partner companies to deliver exceptional outcomes for our clients. Drive business development initiatives, advocating for our services and contributing to bid preparation. Foster strong relationships with clients and third parties, enhancing our reputation and securing new opportunities. Champion our company's capabilities internally and externally, promoting my client's services to current and prospective clients. Ideal Candidate Profile Hold a degree in Environmental Science or related field. Membership of relevant professional bodies such as IEMA, with Chartered Environmentalist or Chartered Scientist status preferred. Proven experience in coordinating Environmental Impact Assessments across different sectors. Sound knowledge of the UK planning system and consents processes, with practical experience in assembling Environmental Statements. Strong analytical, communication, and leadership skills, with the ability to work collaboratively in multidisciplinary teams. Commercial acumen and a track record of success in environmental consultancy procurement. Rewards & Benefits In return for your hard work and dedication, my client offers a highly competitive salary and a comprehensive benefits package. This is an exceptional opportunity to join a forward-thinking organization with ambitious growth plans. You'll receive extensive training, ample opportunities for career advancement, and the chance to shape the future of the business. If you're ready to take the next step in your sustainability career, we encourage you to reach out for a confidential discussion about this exciting opportunity. Let's explore how you can contribute to my client's growth and make a meaningful impact on the world around us. This is one of a number of exciting positions currently available via JSM Associates. JSM offers an extensive range of jobs in the areas of Environmental and Sustainability, including ESG, EIA and Ecology, Contaminated Land, Environmental Planning, Air Quality and Noise. Phone - Email - Website - Twitter LinkedIn
Aug 14, 2025
Full time
Exciting Opportunity: Join a rapidly growing Environmental Management and Assessment Team! Are you ready to take your career to new heights? My client's Environmental Management and Assessment Team is expanding, and hence on the lookout for passionate individuals at Principal and Senior levels to join their team across multiple locations in the UK. From Exeter to London, Luton to Birmingham, Wakefield to Manchester, this is your chance to be part of a dynamic team making a real difference. As a key member of the team, you'll have the opportunity to work on exciting projects spanning various sectors. From coordinating Environmental Impact Assessments to preparing Environmental Statements and Risk Assessments, you'll play a crucial role in delivering objective-led solutions that drive our business forward. Location Across the UK - Exeter, London, Luton, Birmingham, Wakefield, Manchester Responsibilities & Tasks Lead the coordination of Environmental Impact Assessments, ensuring high standards of safety, quality, and environmental responsibility. Prepare Environmental Statements, Management Plans, and Risk Assessments, demonstrating your expertise in environmental science and legislation. Collaborate with internal teams and partner companies to deliver exceptional outcomes for our clients. Drive business development initiatives, advocating for our services and contributing to bid preparation. Foster strong relationships with clients and third parties, enhancing our reputation and securing new opportunities. Champion our company's capabilities internally and externally, promoting my client's services to current and prospective clients. Ideal Candidate Profile Hold a degree in Environmental Science or related field. Membership of relevant professional bodies such as IEMA, with Chartered Environmentalist or Chartered Scientist status preferred. Proven experience in coordinating Environmental Impact Assessments across different sectors. Sound knowledge of the UK planning system and consents processes, with practical experience in assembling Environmental Statements. Strong analytical, communication, and leadership skills, with the ability to work collaboratively in multidisciplinary teams. Commercial acumen and a track record of success in environmental consultancy procurement. Rewards & Benefits In return for your hard work and dedication, my client offers a highly competitive salary and a comprehensive benefits package. This is an exceptional opportunity to join a forward-thinking organization with ambitious growth plans. You'll receive extensive training, ample opportunities for career advancement, and the chance to shape the future of the business. If you're ready to take the next step in your sustainability career, we encourage you to reach out for a confidential discussion about this exciting opportunity. Let's explore how you can contribute to my client's growth and make a meaningful impact on the world around us. This is one of a number of exciting positions currently available via JSM Associates. JSM offers an extensive range of jobs in the areas of Environmental and Sustainability, including ESG, EIA and Ecology, Contaminated Land, Environmental Planning, Air Quality and Noise. Phone - Email - Website - Twitter LinkedIn
Life and Pensions Technology Principal Consultant We believe in the power of ingenuity to build a positive human future. As strategies, technologies, and innovation collide, we create opportunity from complexity. Our teams of interdisciplinary experts combine innovative thinking and breakthrough technologies to progress further, faster. Our clients adapt and transform, and together we achieve enduring results. We are over 4,000 strategists, innovators, designers, consultants, digital experts, scientists, engineers, and technologists. And we have deep expertise in consumer and manufacturing, defence and security, energy and utilities, financial services, government and public services, health and life sciences, and transport. Our teams operate globally from offices across the UK, Ireland, US, Nordics, and Netherlands. PA. Bringing Ingenuity to Life. Hybrid working - our approach is to be in the office or on client site a minimum of 2 days per week. However, the actual time you spend and where you spend it will vary by role or assignment, including up to 5 days per week on a client site. Travel to client site will be necessary as and when the client requires We operate in a hybrid working environment where we come into a client site or office, at least 2-3 days per week. This role will be aligned to our London Victoria office Do you want to be part of an explosive growth journey? Would you like to work in a high performing team where your role involves combining strategy, change, implementation, and technical skills? We are looking for an exceptional Principal Consultant to join our IT Sourcing & Corporate Services capability. You will be instrumental in supporting the continued growth our Life and Pensions business, delivering high-impact consulting projects, and shaping the future of our practice. You will work closely with clients across the L&P sector to understand their needs and challenges, develop innovative strategies, and implement solutions that drive real business value. You'll work across a variety of transformation focused engagements, from taking new products and propositions to market, optimising operating models and technology platforms, and leveraging data to create impactful solutions. You will have opportunity to: Lead and deliver large-scale (IT) transformation programmes within the L&P sector. Collaborate with a high-performing team to create and implement innovative solutions. Develop new business opportunities and contribute to the growth of our L&P practice. Engage with senior stakeholders to understand their strategic objectives and provide expert advice. Stay ahead of industry trends and continuously develop your own expertise. Qualifications Strong management consulting background Extensive experience and comprehensive knowledge in Life and Pension Sector Broad knowledge of the L&P third-party and technology services marketplace and experience across the outsourcing lifecycle, including business cases and cost models (strategy, delivery, transition, service optimisation and remediation); Ability to lead definition business and IT services, requirements and SLAs; Proven track record of delivering transformation in areas such as new products and propositions, operating models, sourcing, platform and data modernisation, post-merger integration. Strong analytical and problem-solving skills, with the ability to develop creative solutions. Excellent communication and stakeholder management skills. Ability to work collaboratively in a fast-paced and dynamic environment. We know the skill-gap and 'somewhat need to tick every box' can get in the way of meeting brilliant candidates, so please don't hesitate to apply - we'd love to hear from you. Apply today by completing our online application Additional information Life At PA encompasses our peoples' experience at PA. It's about how we enrich peoples' working lives by giving them access to unique people and growth opportunities and purpose led meaningful work. Our purpose guides how we work with our clients and our teams, and support our communities, to deliver insight and impact, solving the world's most complex challenges. We're focused on building a workplace that values human difference and diverse mindsets, and a culture of inclusion and equality that unlocks the potential in our people so everyone can be their best self. We are dedicated to supporting the physical, emotional, social and financial well-being of our people. Check out some of our extensive benefits: Health and lifestyle perks accompanying private healthcare for you and your family 25 days annual leave (plus a bonus half day on Christmas Eve) with the opportunity to buy 5 additional days Generous company pension scheme Opportunity to get involved with community and charity-based initiatives Annual performance-based bonus PA share ownership Tax efficient benefits (cycle to work, give as you earn) We're committed to advancing equality.We recruit, retain, reward and develop our people based solely on their abilities and contributions and without reference to their age, background, disability, genetic information, parental or family status, religion or belief, race, ethnicity, nationality, sex, sexual orientation, gender identity (or expression), political belief, veteran status, or by any other range of human difference brought about by identity and experience. We welcome applications from underrepresented groups. Adjustments or accommodations - Should you need any adjustments or accommodations to the recruitment process, at either application or interview, please contact us on
Aug 14, 2025
Full time
Life and Pensions Technology Principal Consultant We believe in the power of ingenuity to build a positive human future. As strategies, technologies, and innovation collide, we create opportunity from complexity. Our teams of interdisciplinary experts combine innovative thinking and breakthrough technologies to progress further, faster. Our clients adapt and transform, and together we achieve enduring results. We are over 4,000 strategists, innovators, designers, consultants, digital experts, scientists, engineers, and technologists. And we have deep expertise in consumer and manufacturing, defence and security, energy and utilities, financial services, government and public services, health and life sciences, and transport. Our teams operate globally from offices across the UK, Ireland, US, Nordics, and Netherlands. PA. Bringing Ingenuity to Life. Hybrid working - our approach is to be in the office or on client site a minimum of 2 days per week. However, the actual time you spend and where you spend it will vary by role or assignment, including up to 5 days per week on a client site. Travel to client site will be necessary as and when the client requires We operate in a hybrid working environment where we come into a client site or office, at least 2-3 days per week. This role will be aligned to our London Victoria office Do you want to be part of an explosive growth journey? Would you like to work in a high performing team where your role involves combining strategy, change, implementation, and technical skills? We are looking for an exceptional Principal Consultant to join our IT Sourcing & Corporate Services capability. You will be instrumental in supporting the continued growth our Life and Pensions business, delivering high-impact consulting projects, and shaping the future of our practice. You will work closely with clients across the L&P sector to understand their needs and challenges, develop innovative strategies, and implement solutions that drive real business value. You'll work across a variety of transformation focused engagements, from taking new products and propositions to market, optimising operating models and technology platforms, and leveraging data to create impactful solutions. You will have opportunity to: Lead and deliver large-scale (IT) transformation programmes within the L&P sector. Collaborate with a high-performing team to create and implement innovative solutions. Develop new business opportunities and contribute to the growth of our L&P practice. Engage with senior stakeholders to understand their strategic objectives and provide expert advice. Stay ahead of industry trends and continuously develop your own expertise. Qualifications Strong management consulting background Extensive experience and comprehensive knowledge in Life and Pension Sector Broad knowledge of the L&P third-party and technology services marketplace and experience across the outsourcing lifecycle, including business cases and cost models (strategy, delivery, transition, service optimisation and remediation); Ability to lead definition business and IT services, requirements and SLAs; Proven track record of delivering transformation in areas such as new products and propositions, operating models, sourcing, platform and data modernisation, post-merger integration. Strong analytical and problem-solving skills, with the ability to develop creative solutions. Excellent communication and stakeholder management skills. Ability to work collaboratively in a fast-paced and dynamic environment. We know the skill-gap and 'somewhat need to tick every box' can get in the way of meeting brilliant candidates, so please don't hesitate to apply - we'd love to hear from you. Apply today by completing our online application Additional information Life At PA encompasses our peoples' experience at PA. It's about how we enrich peoples' working lives by giving them access to unique people and growth opportunities and purpose led meaningful work. Our purpose guides how we work with our clients and our teams, and support our communities, to deliver insight and impact, solving the world's most complex challenges. We're focused on building a workplace that values human difference and diverse mindsets, and a culture of inclusion and equality that unlocks the potential in our people so everyone can be their best self. We are dedicated to supporting the physical, emotional, social and financial well-being of our people. Check out some of our extensive benefits: Health and lifestyle perks accompanying private healthcare for you and your family 25 days annual leave (plus a bonus half day on Christmas Eve) with the opportunity to buy 5 additional days Generous company pension scheme Opportunity to get involved with community and charity-based initiatives Annual performance-based bonus PA share ownership Tax efficient benefits (cycle to work, give as you earn) We're committed to advancing equality.We recruit, retain, reward and develop our people based solely on their abilities and contributions and without reference to their age, background, disability, genetic information, parental or family status, religion or belief, race, ethnicity, nationality, sex, sexual orientation, gender identity (or expression), political belief, veteran status, or by any other range of human difference brought about by identity and experience. We welcome applications from underrepresented groups. Adjustments or accommodations - Should you need any adjustments or accommodations to the recruitment process, at either application or interview, please contact us on
Associate Principal Scientist Material Sciences page is loaded Associate Principal Scientist Material Sciences Apply locations Reading, United Kingdom time type Full time posted on Posted Yesterday job requisition id R-145178 Job Description Are You Ready to Make an Impact at RSSL? Join Our Mission to Transform Lives Through Science, Innovation and Collaboration At Reading Scientific Services Ltd (RSSL), we lead the way in scientific analysis, research, consultancy, and training. We provide services to the food, pharmaceutical, and consumer goods industries, as well as our parent company, Mondelez International. RSSL is dedicated to delivering world-class scientific solutions and outstanding customer service. Recognised for our excellence, we were awarded CRO of the Year at the 2023 OBN Awards, adding to our previous accolades Employer of the Year, Enlightened Employer and Women in Business. If you are passionate about driving innovation and making a real impact, RSSL is the place for you! Purpose: This role will provide expert technical guidance in the area of physical sciences to support Mondelez /RSSL's business objectives . This will require evaluation of emerging technologies to drive new / improved service offerings (e.g. manufacturing processes, NPD, analytical methodology ) and provide expert scientific consultancy . Responsibilities will include complex analytical investigative projects, keeping abreast of scientific developments in the physical sciences area and representing the business externally, e.g. at relevant scientific symposia and expert working groups. In-depth scientific understanding as well as practical experience in key analytical techniques will be required , to include specifically rheology, texture, and thermal analysis, with additional working knowledge of particle size analysis and low resolution NMR. Complex data/result interpretation and presentation to stakeholders will also be undertaken. The position holder will be member of the RSSL team and primarily based in Reading, UK. However, some travel may be required either within the UK or overseas. This role is a key contributor for the ongoing financial, operational and analytical success of the businesses Primary Accountabilities / Responsibilities: Functional/Technical Provide expert consultancy both internally & externally . Actively guide portfolio of analytical techniques globally to ensure delivery of world-class material Sciences capabilities. Significantly impact direction of work done by others in area of expertise . Be a "point person" for rheology, texture, and thermal analysis at Reading. Liaise across the business to undertake a range of specialist projects . Guide complex analysis & interpretation of data for both standard and emergency analysis. Ensure timely delivery of high quality data against project timelines. Independently propose solutions to time conflicts. Liaise with line management, business development managers and clients to ensure effective communication of incoming requests as well as results and actionable next steps. Work with clients to help solve problems. Upskill others in the team to deliver complex projects in area of expertise Leadership, Communication & Influence Strong influencing, networking and stakeholder management Provide expert advice and lead client and stake holders meetings as required . Make an authoritative and expert scientific contribution to business strategy, research and analysis Deliver presentations of data & strategy to senior technical stakeholders e.g. directors, vice - presidents . Present complex scientific data as dictated by the business needs at RSSL, at clients' facilities, or at external meetings/ seminars to raise your own profile and RSSL's reputation in the industry. Represent and exert influence on behalf of RSSL/ Mondelēz through involvement in external scientific institutions, government bodies & industry relevant committees Closely monitor scientific developments within the field of expertise through e.g. involvement in external scientific institutions, government bodies & industry relevant committees. To evaluate emerging scientific and sustainability trends & make recommendations to ensure Mondelēz / RSSL remain at the forefront Q uality, Environment, Health & Safety Work to the highest standards of safety and quality by ensuring that appropriate COSHHs , risk assessments and SOPs are understood and followed. To proactively identify and resolve Quality issues in area of expertise T o complete assigned quality actions on a timely manner, including review and approval Understand and provide technical regulatory leadership in client audits To promote the maintenance of a clean, tidy and safe wo r king environment To understand and work to the requirements of GMP and UKAS Ensure training records are accurate . Knowledge, Skills, Experience and Language Requirements: Educated to Degree or PhD in a relevant scientific discipline or equivalent relevant experience in a laboratory. Proven track record (10 yrs+)of relevant laboratory experience, scientific/technical achievements & developing methods in rheology/ texture/ thermal analysis. In-depth knowledge of both technical area of expertise & business environment including regulatory requirements Good knowledge of laboratory quality and accreditation systems (GMP/UKAS) Strong written and spoken communication skills, with the ability to influence, network and manage internal/external relationships. Excellent organisational skills including time management and priority setting. Ability to deliver projects/work within tight timescales and ability to motivate and mentor junior scientific staff. Technical credibility to develop good working relationships with internal and external clients.Ability to direct complex analytical problem solving High levels of business acumen with strong ability to interpret, deliver and create new business opportunities. Proven experience of strategic planning and delivery Computer literate in standard MS office applications Visionary Leadership, evidence of inspiring a team to achieve excellence in the delivery of projects Recognised specialist - through Fellow / Member of relevant professional body, History of published work in relevant scientific journals. The individual in this position is a recognized expert in their discipline and has a demonstrated track record of applying their knowledge across different business areas. Proven experience of authoring technical reports and presenting findings at relevant symposia. Career evidence of report publication, with a track record of success. Experience of working for, or with, a CRO English fluency (written and spoken) More about this role In return for your commitment, drive and enthusiasm, we offer an attractive benefits package within a highly successful international business that offers financial rewards and resources, including: Opportunities to learn and develop Performance Related Bonus scheme Contributory pension (between 8% to 11% employer contribution) Life assurance Private Medical (Self) 27 days holiday allowance (possibility to buy 5 extra days) + bank holidays Employee Assistance Programme (EAP) A flexible benefits programme (Gym discounts, private health insurance, restaurant discounts, etc). No Relocation support available Business Unit Summary Reading Scientific Services Ltd (RSSL) is a cutting-edge contract research organisation (CRO), providing research, analysis and consultancy to the food, consumer goods and life science sectors. Whether we are creating new products, validating medicines or solving investigations, we take pride in being a leader in our field, serving clients from across 70 countries.Enriched by our parent company, Mondelēz International, our team are committed to transforming lives through science, innovation and collaboration. Curious about us and want to learn more? Please explore: Website YouTube LinkedIn Glassdoor RSSL is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, colour, religion, gender, sexual orientation or preference, gender identity, national origin, disability status, protected veteran status, or any other characteristic protected by law. Job Type RegularAnalytical ScienceScience & Engineering About us RSSL is a leading UK Contract Research Organisation, trusted by the world's most innovative Life Sciences and Food companies to deliver innovative solutions to real world problems to help make our world safer, healthier and more sustainable. Our fast-growing, diverse team of more than 350 scientists, consultants and technical experts work on cutting-edge drug development and food formulation projects to ensure the foods we love, and the medicines we trust, are safe, effective and of the highest quality. We are proud of who we are, the work we do and the impact we make. We're excited about the future. We see opportunity in change, possibility in science and the potential to transform lives for the better. If you feel the same way, take your next step with us and let's make a positive impact together.
Aug 14, 2025
Full time
Associate Principal Scientist Material Sciences page is loaded Associate Principal Scientist Material Sciences Apply locations Reading, United Kingdom time type Full time posted on Posted Yesterday job requisition id R-145178 Job Description Are You Ready to Make an Impact at RSSL? Join Our Mission to Transform Lives Through Science, Innovation and Collaboration At Reading Scientific Services Ltd (RSSL), we lead the way in scientific analysis, research, consultancy, and training. We provide services to the food, pharmaceutical, and consumer goods industries, as well as our parent company, Mondelez International. RSSL is dedicated to delivering world-class scientific solutions and outstanding customer service. Recognised for our excellence, we were awarded CRO of the Year at the 2023 OBN Awards, adding to our previous accolades Employer of the Year, Enlightened Employer and Women in Business. If you are passionate about driving innovation and making a real impact, RSSL is the place for you! Purpose: This role will provide expert technical guidance in the area of physical sciences to support Mondelez /RSSL's business objectives . This will require evaluation of emerging technologies to drive new / improved service offerings (e.g. manufacturing processes, NPD, analytical methodology ) and provide expert scientific consultancy . Responsibilities will include complex analytical investigative projects, keeping abreast of scientific developments in the physical sciences area and representing the business externally, e.g. at relevant scientific symposia and expert working groups. In-depth scientific understanding as well as practical experience in key analytical techniques will be required , to include specifically rheology, texture, and thermal analysis, with additional working knowledge of particle size analysis and low resolution NMR. Complex data/result interpretation and presentation to stakeholders will also be undertaken. The position holder will be member of the RSSL team and primarily based in Reading, UK. However, some travel may be required either within the UK or overseas. This role is a key contributor for the ongoing financial, operational and analytical success of the businesses Primary Accountabilities / Responsibilities: Functional/Technical Provide expert consultancy both internally & externally . Actively guide portfolio of analytical techniques globally to ensure delivery of world-class material Sciences capabilities. Significantly impact direction of work done by others in area of expertise . Be a "point person" for rheology, texture, and thermal analysis at Reading. Liaise across the business to undertake a range of specialist projects . Guide complex analysis & interpretation of data for both standard and emergency analysis. Ensure timely delivery of high quality data against project timelines. Independently propose solutions to time conflicts. Liaise with line management, business development managers and clients to ensure effective communication of incoming requests as well as results and actionable next steps. Work with clients to help solve problems. Upskill others in the team to deliver complex projects in area of expertise Leadership, Communication & Influence Strong influencing, networking and stakeholder management Provide expert advice and lead client and stake holders meetings as required . Make an authoritative and expert scientific contribution to business strategy, research and analysis Deliver presentations of data & strategy to senior technical stakeholders e.g. directors, vice - presidents . Present complex scientific data as dictated by the business needs at RSSL, at clients' facilities, or at external meetings/ seminars to raise your own profile and RSSL's reputation in the industry. Represent and exert influence on behalf of RSSL/ Mondelēz through involvement in external scientific institutions, government bodies & industry relevant committees Closely monitor scientific developments within the field of expertise through e.g. involvement in external scientific institutions, government bodies & industry relevant committees. To evaluate emerging scientific and sustainability trends & make recommendations to ensure Mondelēz / RSSL remain at the forefront Q uality, Environment, Health & Safety Work to the highest standards of safety and quality by ensuring that appropriate COSHHs , risk assessments and SOPs are understood and followed. To proactively identify and resolve Quality issues in area of expertise T o complete assigned quality actions on a timely manner, including review and approval Understand and provide technical regulatory leadership in client audits To promote the maintenance of a clean, tidy and safe wo r king environment To understand and work to the requirements of GMP and UKAS Ensure training records are accurate . Knowledge, Skills, Experience and Language Requirements: Educated to Degree or PhD in a relevant scientific discipline or equivalent relevant experience in a laboratory. Proven track record (10 yrs+)of relevant laboratory experience, scientific/technical achievements & developing methods in rheology/ texture/ thermal analysis. In-depth knowledge of both technical area of expertise & business environment including regulatory requirements Good knowledge of laboratory quality and accreditation systems (GMP/UKAS) Strong written and spoken communication skills, with the ability to influence, network and manage internal/external relationships. Excellent organisational skills including time management and priority setting. Ability to deliver projects/work within tight timescales and ability to motivate and mentor junior scientific staff. Technical credibility to develop good working relationships with internal and external clients.Ability to direct complex analytical problem solving High levels of business acumen with strong ability to interpret, deliver and create new business opportunities. Proven experience of strategic planning and delivery Computer literate in standard MS office applications Visionary Leadership, evidence of inspiring a team to achieve excellence in the delivery of projects Recognised specialist - through Fellow / Member of relevant professional body, History of published work in relevant scientific journals. The individual in this position is a recognized expert in their discipline and has a demonstrated track record of applying their knowledge across different business areas. Proven experience of authoring technical reports and presenting findings at relevant symposia. Career evidence of report publication, with a track record of success. Experience of working for, or with, a CRO English fluency (written and spoken) More about this role In return for your commitment, drive and enthusiasm, we offer an attractive benefits package within a highly successful international business that offers financial rewards and resources, including: Opportunities to learn and develop Performance Related Bonus scheme Contributory pension (between 8% to 11% employer contribution) Life assurance Private Medical (Self) 27 days holiday allowance (possibility to buy 5 extra days) + bank holidays Employee Assistance Programme (EAP) A flexible benefits programme (Gym discounts, private health insurance, restaurant discounts, etc). No Relocation support available Business Unit Summary Reading Scientific Services Ltd (RSSL) is a cutting-edge contract research organisation (CRO), providing research, analysis and consultancy to the food, consumer goods and life science sectors. Whether we are creating new products, validating medicines or solving investigations, we take pride in being a leader in our field, serving clients from across 70 countries.Enriched by our parent company, Mondelēz International, our team are committed to transforming lives through science, innovation and collaboration. Curious about us and want to learn more? Please explore: Website YouTube LinkedIn Glassdoor RSSL is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, colour, religion, gender, sexual orientation or preference, gender identity, national origin, disability status, protected veteran status, or any other characteristic protected by law. Job Type RegularAnalytical ScienceScience & Engineering About us RSSL is a leading UK Contract Research Organisation, trusted by the world's most innovative Life Sciences and Food companies to deliver innovative solutions to real world problems to help make our world safer, healthier and more sustainable. Our fast-growing, diverse team of more than 350 scientists, consultants and technical experts work on cutting-edge drug development and food formulation projects to ensure the foods we love, and the medicines we trust, are safe, effective and of the highest quality. We are proud of who we are, the work we do and the impact we make. We're excited about the future. We see opportunity in change, possibility in science and the potential to transform lives for the better. If you feel the same way, take your next step with us and let's make a positive impact together.
Mondelez España Galletas Production SLU
Reading, Berkshire
Associate Principal Scientist Material Sciences Are You Ready to Make an Impact at RSSL? Join Our Mission to Transform Lives Through Science, Innovation and Collaboration At Reading Scientific Services Ltd (RSSL), we lead the way in scientific analysis, research, consultancy, and training. We provide services to the food, pharmaceutical, and consumer goods industries, as well as our parent company, Mondelez International. RSSL is dedicated to delivering world-class scientific solutions and outstanding customer service. Recognised for our excellence, we were awarded CRO of the Year at the 2023 OBN Awards, adding to our previous accolades Employer of the Year, Enlightened Employer and Women in Business. If you are passionate about driving innovation and making a real impact, RSSL is the place for you! Purpose: This role will provide expert technical guidance in the area of physical sciences to support Mondelez /RSSL's business objectives . This will require evaluation of emerging technologies to drive new / improved service offerings (e.g. manufacturing processes, NPD, analytical methodology ) and provide expert scientific consultancy . Responsibilities will include complex analytical investigative projects, keeping abreast of scientific developments in the physical sciences area and representing the business externally, e.g. at relevant scientific symposia and expert working groups. In-depth scientific understanding as well as practical experience in key analytical techniques will be required , to include specifically rheology, texture, and thermal analysis, with additional working knowledge of particle size analysis and low resolution NMR. Complex data/result interpretation and presentation to stakeholders will also be undertaken. The position holder will be member of the RSSL team and primarily based in Reading, UK. However, some travel may be required either within the UK or overseas. This role is a key contributor for the ongoing financial, operational and analytical success of the businesses Primary Accountabilities / Responsibilities: Functional/Technical Provide expert consultancy both internally & externally . Actively guide portfolio of analytical techniques globally to ensure delivery of world-class material Sciences capabilities. Significantly impact direction of work done by others in area of expertise . Be a "point person" for rheology, texture, and thermal analysis at Reading. Liaise across the business to undertake a range of specialist projects . Guide complex analysis & interpretation of data for both standard and emergency analysis. Ensure timely delivery of high quality data against project timelines. Independently propose solutions to time conflicts. Liaise with line management, business development managers and clients to ensure effective communication of incoming requests as well as results and actionable next steps. Work with clients to help solve problems. Upskill others in the team to deliver complex projects in area of expertise Leadership, Communication & Influence Strong influencing, networking and stakeholder management Provide expert advice and lead client and stake holders meetings as required . Make an authoritative and expert scientific contribution to business strategy, research and analysis Deliver presentations of data & strategy to senior technical stakeholders e.g. directors, vice - presidents . Present complex scientific data as dictated by the business needs at RSSL, at clients' facilities, or at external meetings/ seminars to raise your own profile and RSSL's reputation in the industry. Represent and exert influence on behalf of RSSL/ Mondelēz through involvement in external scientific institutions, government bodies & industry relevant committees Closely monitor scientific developments within the field of expertise through e.g. involvement in external scientific institutions, government bodies & industry relevant committees. To evaluate emerging scientific and sustainability trends & make recommendations to ensure Mondelēz / RSSL remain at the forefront Work to the highest standards of safety and quality by ensuring that appropriate COSHHs , risk assessments and SOPs are understood and followed. To proactively identify and resolve Quality issues in area of expertise T o complete assigned quality actions on a timely manner, including review and approval Understand and provide technical regulatory leadership in client audits To promote the maintenance of a clean, tidy and safe wo r king environment To understand and work to the requirements of GMP and UKAS Ensure training records are accurate . Knowledge, Skills, Experience and Language Requirements: Educated to Degree or PhD in a relevant scientific discipline or equivalent relevant experience in a laboratory. Proven track record (10 yrs+)of relevant laboratory experience, scientific/technical achievements & developing methods in rheology/ texture/ thermal analysis. In-depth knowledge of both technical area of expertise & business environment including regulatory requirements Good knowledge of laboratory quality and accreditation systems (GMP/UKAS) Strong written and spoken communication skills, with the ability to influence, network and manage internal/external relationships. Excellent organisational skills including time management and priority setting. Ability to deliver projects/work within tight timescales and ability to motivate and mentor junior scientific staff. Technical credibility to develop good working relationships with internal and external clients.Ability to direct complex analytical problem solving High levels of business acumen with strong ability to interpret, deliver and create new business opportunities. Proven experience of strategic planning and delivery Computer literate in standard MS office applications Visionary Leadership, evidence of inspiring a team to achieve excellence in the delivery of projects Recognised specialist - through Fellow / Member of relevant professional body, History of published work in relevant scientific journals. The individual in this position is a recognized expert in their discipline and has a demonstrated track record of applying their knowledge across different business areas. Proven experience of authoring technical reports and presenting findings at relevant symposia. Career evidence of report publication, with a track record of success. Experience of working for, or with, a CRO English fluency (written and spoken) More about this role In return for your commitment, drive and enthusiasm, we offer an attractive benefits package within a highly successful international business that offers financial rewards and resources, including: Opportunities to learn and develop Performance Related Bonus scheme Contributory pension (between 8% to 11% employer contribution) Life assurance Private Medical (Self) 27 days holiday allowance (possibility to buy 5 extra days) + bank holidays Employee Assistance Programme (EAP) Business Unit Summary Reading Scientific Services Ltd (RSSL) is a cutting-edge contract research organisation (CRO), providing research, analysis and consultancy to the food, consumer goods and life science sectors. Whether we are creating new products, validating medicines or solving investigations, we take pride in being a leader in our field, serving clients from across 70 countries.Enriched by our parent company, Mondelēz International, our team are committed to transforming lives through science, innovation and collaboration. Curious about us and want to learn more? RSSL is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, colour, religion, gender, sexual orientation or preference, gender identity, national origin, disability status, protected veteran status, or any other characteristic protected by law. Job Type RegularAnalytical ScienceScience & Engineering Job Description Are You Ready to Make an Impact at RSSL? Join Our Mission to Transform Lives Through Science, Innovation and Collaboration At Reading Scientific Services Ltd (RSSL), we lead the way in scientific analysis, research, consultancy, and training. We provide services to the food, pharmaceutical, and consumer goods industries, as well as our parent company, Mondelez International. RSSL is dedicated to delivering world-class scientific solutions and outstanding customer service. Recognised for our excellence, we were awarded CRO of the Year at the 2023 OBN Awards, adding to our previous accolades Employer of the Year, Enlightened Employer and Women in Business. If you are passionate about driving innovation and making a real impact, RSSL is the place for you! Purpose: This role will provide expert technical guidance in the area of physical sciences to support Mondelez /RSSL's business objectives . This will require evaluation of emerging technologies to drive new / improved service offerings (e.g. manufacturing processes, NPD, analytical methodology ) and provide expert scientific consultancy . Responsibilities will include complex analytical investigative projects, keeping abreast of scientific developments in the physical sciences area and representing the business externally, e.g . click apply for full job details
Aug 14, 2025
Full time
Associate Principal Scientist Material Sciences Are You Ready to Make an Impact at RSSL? Join Our Mission to Transform Lives Through Science, Innovation and Collaboration At Reading Scientific Services Ltd (RSSL), we lead the way in scientific analysis, research, consultancy, and training. We provide services to the food, pharmaceutical, and consumer goods industries, as well as our parent company, Mondelez International. RSSL is dedicated to delivering world-class scientific solutions and outstanding customer service. Recognised for our excellence, we were awarded CRO of the Year at the 2023 OBN Awards, adding to our previous accolades Employer of the Year, Enlightened Employer and Women in Business. If you are passionate about driving innovation and making a real impact, RSSL is the place for you! Purpose: This role will provide expert technical guidance in the area of physical sciences to support Mondelez /RSSL's business objectives . This will require evaluation of emerging technologies to drive new / improved service offerings (e.g. manufacturing processes, NPD, analytical methodology ) and provide expert scientific consultancy . Responsibilities will include complex analytical investigative projects, keeping abreast of scientific developments in the physical sciences area and representing the business externally, e.g. at relevant scientific symposia and expert working groups. In-depth scientific understanding as well as practical experience in key analytical techniques will be required , to include specifically rheology, texture, and thermal analysis, with additional working knowledge of particle size analysis and low resolution NMR. Complex data/result interpretation and presentation to stakeholders will also be undertaken. The position holder will be member of the RSSL team and primarily based in Reading, UK. However, some travel may be required either within the UK or overseas. This role is a key contributor for the ongoing financial, operational and analytical success of the businesses Primary Accountabilities / Responsibilities: Functional/Technical Provide expert consultancy both internally & externally . Actively guide portfolio of analytical techniques globally to ensure delivery of world-class material Sciences capabilities. Significantly impact direction of work done by others in area of expertise . Be a "point person" for rheology, texture, and thermal analysis at Reading. Liaise across the business to undertake a range of specialist projects . Guide complex analysis & interpretation of data for both standard and emergency analysis. Ensure timely delivery of high quality data against project timelines. Independently propose solutions to time conflicts. Liaise with line management, business development managers and clients to ensure effective communication of incoming requests as well as results and actionable next steps. Work with clients to help solve problems. Upskill others in the team to deliver complex projects in area of expertise Leadership, Communication & Influence Strong influencing, networking and stakeholder management Provide expert advice and lead client and stake holders meetings as required . Make an authoritative and expert scientific contribution to business strategy, research and analysis Deliver presentations of data & strategy to senior technical stakeholders e.g. directors, vice - presidents . Present complex scientific data as dictated by the business needs at RSSL, at clients' facilities, or at external meetings/ seminars to raise your own profile and RSSL's reputation in the industry. Represent and exert influence on behalf of RSSL/ Mondelēz through involvement in external scientific institutions, government bodies & industry relevant committees Closely monitor scientific developments within the field of expertise through e.g. involvement in external scientific institutions, government bodies & industry relevant committees. To evaluate emerging scientific and sustainability trends & make recommendations to ensure Mondelēz / RSSL remain at the forefront Work to the highest standards of safety and quality by ensuring that appropriate COSHHs , risk assessments and SOPs are understood and followed. To proactively identify and resolve Quality issues in area of expertise T o complete assigned quality actions on a timely manner, including review and approval Understand and provide technical regulatory leadership in client audits To promote the maintenance of a clean, tidy and safe wo r king environment To understand and work to the requirements of GMP and UKAS Ensure training records are accurate . Knowledge, Skills, Experience and Language Requirements: Educated to Degree or PhD in a relevant scientific discipline or equivalent relevant experience in a laboratory. Proven track record (10 yrs+)of relevant laboratory experience, scientific/technical achievements & developing methods in rheology/ texture/ thermal analysis. In-depth knowledge of both technical area of expertise & business environment including regulatory requirements Good knowledge of laboratory quality and accreditation systems (GMP/UKAS) Strong written and spoken communication skills, with the ability to influence, network and manage internal/external relationships. Excellent organisational skills including time management and priority setting. Ability to deliver projects/work within tight timescales and ability to motivate and mentor junior scientific staff. Technical credibility to develop good working relationships with internal and external clients.Ability to direct complex analytical problem solving High levels of business acumen with strong ability to interpret, deliver and create new business opportunities. Proven experience of strategic planning and delivery Computer literate in standard MS office applications Visionary Leadership, evidence of inspiring a team to achieve excellence in the delivery of projects Recognised specialist - through Fellow / Member of relevant professional body, History of published work in relevant scientific journals. The individual in this position is a recognized expert in their discipline and has a demonstrated track record of applying their knowledge across different business areas. Proven experience of authoring technical reports and presenting findings at relevant symposia. Career evidence of report publication, with a track record of success. Experience of working for, or with, a CRO English fluency (written and spoken) More about this role In return for your commitment, drive and enthusiasm, we offer an attractive benefits package within a highly successful international business that offers financial rewards and resources, including: Opportunities to learn and develop Performance Related Bonus scheme Contributory pension (between 8% to 11% employer contribution) Life assurance Private Medical (Self) 27 days holiday allowance (possibility to buy 5 extra days) + bank holidays Employee Assistance Programme (EAP) Business Unit Summary Reading Scientific Services Ltd (RSSL) is a cutting-edge contract research organisation (CRO), providing research, analysis and consultancy to the food, consumer goods and life science sectors. Whether we are creating new products, validating medicines or solving investigations, we take pride in being a leader in our field, serving clients from across 70 countries.Enriched by our parent company, Mondelēz International, our team are committed to transforming lives through science, innovation and collaboration. Curious about us and want to learn more? RSSL is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, colour, religion, gender, sexual orientation or preference, gender identity, national origin, disability status, protected veteran status, or any other characteristic protected by law. Job Type RegularAnalytical ScienceScience & Engineering Job Description Are You Ready to Make an Impact at RSSL? Join Our Mission to Transform Lives Through Science, Innovation and Collaboration At Reading Scientific Services Ltd (RSSL), we lead the way in scientific analysis, research, consultancy, and training. We provide services to the food, pharmaceutical, and consumer goods industries, as well as our parent company, Mondelez International. RSSL is dedicated to delivering world-class scientific solutions and outstanding customer service. Recognised for our excellence, we were awarded CRO of the Year at the 2023 OBN Awards, adding to our previous accolades Employer of the Year, Enlightened Employer and Women in Business. If you are passionate about driving innovation and making a real impact, RSSL is the place for you! Purpose: This role will provide expert technical guidance in the area of physical sciences to support Mondelez /RSSL's business objectives . This will require evaluation of emerging technologies to drive new / improved service offerings (e.g. manufacturing processes, NPD, analytical methodology ) and provide expert scientific consultancy . Responsibilities will include complex analytical investigative projects, keeping abreast of scientific developments in the physical sciences area and representing the business externally, e.g . click apply for full job details
About TalentNeuron TalentNeuron is the world's leading provider of labor market analytics, delivering high-fidelity talent data on an unmatched global scale. TalentNeuron delivers actionable talent insight for every region of the world covering countries that collectively represent more than 90% of the world's GDP. Through deep investments in machine learning and artificial intelligence, our technology platform ingests and normalizes hundreds of millions of structured and unstructured data points each day, delivering critical talent insights in support of workforce planning, strategic skills analysis, location optimization, DEI tactics, and sourcing strategies for local, regional, and global talent. These insights can be delivered to clients via software as a service, data as a service, or fully custom research efforts from our team of expert data scientists and advisors. Reporting to the Chief Revenue Officer, the VP of Customer Experience will lead the post-sale customer journey from contract signing through renewal and expansion. This commercially focused leader will have responsibility to coach, mentor and train functional leaders to identify white space, cadence and value driven customer engagement, create and measure against mutually agreed upon north stars, develop and deploy outcome driven success plans and accurately forecast renewal and growth metrics. Our Core Values Humanity First: We lead with humanity. We foster empathy, kindness, respect, and inclusiveness in all contexts and support one another. Customers at the Core: We engage in meaningful and constant dialogue with clients to deeply understand and anticipate their needs, and consistently deliver exceptional value. We operate with integrity and do what's right for our clients, no matter how difficult. Diverse Minds, One Team: We are curious and seek different perspectives and find common ground, but we act, succeed, fail, and celebrate as one. We openly collaborate, communicate, debate, and compromise across groups. Pioneering Innovation: We take risks, fail fast, and learn from our experiments. We champion change and evolution without fear and inspire a culture where innovation thrives. Resilient Perseverance: We think creatively and pragmatically to find solutions, remove barriers, and overcome obstacles. We are equally accountable for the results of the whole team and for our individual commitments, and we find a way to get things done by embracing a "yes we can" attitude. What you will do: Own the post sale customer retention commercial strategy to retain and expand current customers. Develop and implement a company-wide customer experience strategy aligned with business goals. Lead and mentor teams across Account Management, Professional Services and Support Establish and maintain KPIs and metrics to measure gross and net retention, customer satisfaction, Utilizationand Net Promoter Score (NPS). Collaborate with Product, Product Marketing, Support and Revenue Operationsto ensure customer feedback informs decision-making. Champion a culture of data driven customer-centricity across all departments. Own the design and optimization of customer journeys across digital and physical channels. Drive innovation in customer engagement through technology, personalization, and proactive service. Present insights and strategic recommendations to executive leadership and the board. What You Will Bring: A commercial mindset, focused on retaining and expanding TN customer base. A role up your sleeve's mentality with a bias toward action 10+ years of experience in customer experience, customer success, or related fields, with at least 5 years in a senior leadership role. Proven track record of improving customer satisfaction and retention metrics. Strong analytical skills and experience with CX tools and platforms (e.g., Zendesk, Salesforce, Qualtrics). Exceptional communication and leadership abilities. Experience in architecting and rebuilding customer experience organizations through value creation Bachelor's degree required; MBA or equivalent preferred. £200,000 - £210,000 a year If you're a Customer Experience professional who's ready to take on a challenging yet rewarding role, we encourage you to apply. At TalentNeuron, you'll have the opportunity to work with top-tier professionals, manage diverse relationships, and make a significant impact. We believe in nurturing talent, fostering a collaborative environment, and recognizing the achievements of our team. Join us, exceed your sales goals, and be a part of our success story. Apply now and let's shape the future of TalentNeuron together. We're an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.
Aug 13, 2025
Full time
About TalentNeuron TalentNeuron is the world's leading provider of labor market analytics, delivering high-fidelity talent data on an unmatched global scale. TalentNeuron delivers actionable talent insight for every region of the world covering countries that collectively represent more than 90% of the world's GDP. Through deep investments in machine learning and artificial intelligence, our technology platform ingests and normalizes hundreds of millions of structured and unstructured data points each day, delivering critical talent insights in support of workforce planning, strategic skills analysis, location optimization, DEI tactics, and sourcing strategies for local, regional, and global talent. These insights can be delivered to clients via software as a service, data as a service, or fully custom research efforts from our team of expert data scientists and advisors. Reporting to the Chief Revenue Officer, the VP of Customer Experience will lead the post-sale customer journey from contract signing through renewal and expansion. This commercially focused leader will have responsibility to coach, mentor and train functional leaders to identify white space, cadence and value driven customer engagement, create and measure against mutually agreed upon north stars, develop and deploy outcome driven success plans and accurately forecast renewal and growth metrics. Our Core Values Humanity First: We lead with humanity. We foster empathy, kindness, respect, and inclusiveness in all contexts and support one another. Customers at the Core: We engage in meaningful and constant dialogue with clients to deeply understand and anticipate their needs, and consistently deliver exceptional value. We operate with integrity and do what's right for our clients, no matter how difficult. Diverse Minds, One Team: We are curious and seek different perspectives and find common ground, but we act, succeed, fail, and celebrate as one. We openly collaborate, communicate, debate, and compromise across groups. Pioneering Innovation: We take risks, fail fast, and learn from our experiments. We champion change and evolution without fear and inspire a culture where innovation thrives. Resilient Perseverance: We think creatively and pragmatically to find solutions, remove barriers, and overcome obstacles. We are equally accountable for the results of the whole team and for our individual commitments, and we find a way to get things done by embracing a "yes we can" attitude. What you will do: Own the post sale customer retention commercial strategy to retain and expand current customers. Develop and implement a company-wide customer experience strategy aligned with business goals. Lead and mentor teams across Account Management, Professional Services and Support Establish and maintain KPIs and metrics to measure gross and net retention, customer satisfaction, Utilizationand Net Promoter Score (NPS). Collaborate with Product, Product Marketing, Support and Revenue Operationsto ensure customer feedback informs decision-making. Champion a culture of data driven customer-centricity across all departments. Own the design and optimization of customer journeys across digital and physical channels. Drive innovation in customer engagement through technology, personalization, and proactive service. Present insights and strategic recommendations to executive leadership and the board. What You Will Bring: A commercial mindset, focused on retaining and expanding TN customer base. A role up your sleeve's mentality with a bias toward action 10+ years of experience in customer experience, customer success, or related fields, with at least 5 years in a senior leadership role. Proven track record of improving customer satisfaction and retention metrics. Strong analytical skills and experience with CX tools and platforms (e.g., Zendesk, Salesforce, Qualtrics). Exceptional communication and leadership abilities. Experience in architecting and rebuilding customer experience organizations through value creation Bachelor's degree required; MBA or equivalent preferred. £200,000 - £210,000 a year If you're a Customer Experience professional who's ready to take on a challenging yet rewarding role, we encourage you to apply. At TalentNeuron, you'll have the opportunity to work with top-tier professionals, manage diverse relationships, and make a significant impact. We believe in nurturing talent, fostering a collaborative environment, and recognizing the achievements of our team. Join us, exceed your sales goals, and be a part of our success story. Apply now and let's shape the future of TalentNeuron together. We're an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.
