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CK GROUP
Principal Scientist
CK GROUP Oxford, Oxfordshire
CK Group are recruiting for an experienced and dynamic Scientist, at either Senior/ Principal level, to join an early-stage biotechnology start-up, based in Oxford, on a permanent basis. Th e Company: Our client is an early-stage biotechnology start up, combining artificial intelligence (AI), and advanced high-throughput TCR screening techniques to revolutionise the treatment of solid cancers. Location : Oxford. The Role: To lead the in vivo and in vitro validation of T-cell engagers, and help drive forward the development of TCR engineering and processes. Responsibilities : To perform high-throughput TCR display methods by purifying recombinant TCRs. Carry out protein characterisation (expression, purification and biophysical analysis). Design and characterise TCRs for disease targets. Oversee lab protocols and technical documents. To be hands-on in the lab and manage tissue culture preparations. Skills in data analysis (using software R) for Next Gen Sequencing analysis - desirable. Your Background: PhD qualified (biochemistry, immunology, cell biology) plus strong laboratory experience (academia and industry). Experience in in vivo and in vitro validation of T-cell engagers (TCEs). Experience in Investigational New Drug (IND-enabling/ approval) - ESSENTIAL. Expertise in cell and immunological assays (flow cytometry, ELISA) with knowledge around cloning and PCR. Strong background in protein characterisation and biophysical characterisation. Benefits : Competitive salary, option for home working (as per project demands), stock options. Apply: It is essential that applicants hold entitlement to work in the UK. Please quote job reference in all correspondence. If this position isn't suitable but you are looking for a new role, or if you are interested in seeing what opportunities are out there, head over to our LinkedIn page (cka-group) and follow us to see our latest jobs and company news. INDCP
Jul 03, 2025
Full time
CK Group are recruiting for an experienced and dynamic Scientist, at either Senior/ Principal level, to join an early-stage biotechnology start-up, based in Oxford, on a permanent basis. Th e Company: Our client is an early-stage biotechnology start up, combining artificial intelligence (AI), and advanced high-throughput TCR screening techniques to revolutionise the treatment of solid cancers. Location : Oxford. The Role: To lead the in vivo and in vitro validation of T-cell engagers, and help drive forward the development of TCR engineering and processes. Responsibilities : To perform high-throughput TCR display methods by purifying recombinant TCRs. Carry out protein characterisation (expression, purification and biophysical analysis). Design and characterise TCRs for disease targets. Oversee lab protocols and technical documents. To be hands-on in the lab and manage tissue culture preparations. Skills in data analysis (using software R) for Next Gen Sequencing analysis - desirable. Your Background: PhD qualified (biochemistry, immunology, cell biology) plus strong laboratory experience (academia and industry). Experience in in vivo and in vitro validation of T-cell engagers (TCEs). Experience in Investigational New Drug (IND-enabling/ approval) - ESSENTIAL. Expertise in cell and immunological assays (flow cytometry, ELISA) with knowledge around cloning and PCR. Strong background in protein characterisation and biophysical characterisation. Benefits : Competitive salary, option for home working (as per project demands), stock options. Apply: It is essential that applicants hold entitlement to work in the UK. Please quote job reference in all correspondence. If this position isn't suitable but you are looking for a new role, or if you are interested in seeing what opportunities are out there, head over to our LinkedIn page (cka-group) and follow us to see our latest jobs and company news. INDCP
WuXi AppTec
Senior Manager/Associate Director, CMC Project Management
WuXi AppTec
The Senior Manager/Associate Director Project Manager will be responsible for managing projects within STA, WuXi's API and Drug Product development and manufacturing division. Leads the orderly progression of projects from the proposal stage through project completion by interacting with the client, technical team and business development team. The incumbent will also participate in business development activities such as visiting existing or new clients and promoting STA's services in conferences/trade shows. Please note this is a remote (work from home) position within the UK. Lead all project initiation and planning efforts. Participate in the implementation and execution of a given project. Establishes project objectives, timelines and deliverables. Defines project tasks and resource requirements. Closely monitor/control project progression to ensure project is completed on schedule and within budget. Reports project progress to all key stakeholders. Supports the technical team to investigate any project challenges by necessary risk assessment tools & techniques, then implements corrective measures. Serves as liaison with client contacts, manages day-to-day communications and organizes project team meetings. Represents company in project meetings, prepares meeting agenda and minutes, and follows up on action items. Evaluates and assesses project results and provides recommendations for future improvements. Provides support to the business development team joining customer visits, conferences or tradeshows. Prepare Quotations/Proposals/Change Orders with inputs from key stakeholders for existing relationships. Education and Experience: Master's (MS) or PhD in life sciences; chemistry preferred A minimum of 10 years pharmaceutical or CRO/CMO industry experience, preferably in API process R&D and manufacturing and/or Drug Product R&D and manufacturing. Prior experience in project management or managing external research collaborations, with PMP certification desired. Candidate should possess strong and effective project management, problem-solving solving and interpersonal skills and have a proven track record working cross-functionally across a wide variety of technical, business, and operational areas. Demonstrates good understanding of the pharmaceutical industry and small molecule drug development. Minimum of 5 years of relevant pharmaceutical or biotech industry experience in CMC process development and/or GMP manufacturing. Working knowledge and understanding of current regulations and industry trends for small molecule, manufacturing, and testing. Oligonucleotide and Solid State Peptide experience a plus. Experience in a Contract Research Organization (CRO) or Contract Manufacturing Organization (CMO) is preferred, but not required. Must have working knowledge of MS Office products, especially MS Project. Independence/Accountability: Must be a self-starter, self-motivated, and highly flexible in this home-based position with 25% travel. Must be organized and detail-oriented. Problem Solving: Proven experience creating and carrying out successful plans and processes to solve complex problems. Leadership Activities: Work closely with team members across all CMC-related business units and with the STA management team to ensure coordination of all efforts and real-time communication with all stakeholders. Communication Skills: Proficiency in English is required. Mandarin is a plus Excellent communication skills (verbal, written, and presentation skills).
Jul 03, 2025
Full time
The Senior Manager/Associate Director Project Manager will be responsible for managing projects within STA, WuXi's API and Drug Product development and manufacturing division. Leads the orderly progression of projects from the proposal stage through project completion by interacting with the client, technical team and business development team. The incumbent will also participate in business development activities such as visiting existing or new clients and promoting STA's services in conferences/trade shows. Please note this is a remote (work from home) position within the UK. Lead all project initiation and planning efforts. Participate in the implementation and execution of a given project. Establishes project objectives, timelines and deliverables. Defines project tasks and resource requirements. Closely monitor/control project progression to ensure project is completed on schedule and within budget. Reports project progress to all key stakeholders. Supports the technical team to investigate any project challenges by necessary risk assessment tools & techniques, then implements corrective measures. Serves as liaison with client contacts, manages day-to-day communications and organizes project team meetings. Represents company in project meetings, prepares meeting agenda and minutes, and follows up on action items. Evaluates and assesses project results and provides recommendations for future improvements. Provides support to the business development team joining customer visits, conferences or tradeshows. Prepare Quotations/Proposals/Change Orders with inputs from key stakeholders for existing relationships. Education and Experience: Master's (MS) or PhD in life sciences; chemistry preferred A minimum of 10 years pharmaceutical or CRO/CMO industry experience, preferably in API process R&D and manufacturing and/or Drug Product R&D and manufacturing. Prior experience in project management or managing external research collaborations, with PMP certification desired. Candidate should possess strong and effective project management, problem-solving solving and interpersonal skills and have a proven track record working cross-functionally across a wide variety of technical, business, and operational areas. Demonstrates good understanding of the pharmaceutical industry and small molecule drug development. Minimum of 5 years of relevant pharmaceutical or biotech industry experience in CMC process development and/or GMP manufacturing. Working knowledge and understanding of current regulations and industry trends for small molecule, manufacturing, and testing. Oligonucleotide and Solid State Peptide experience a plus. Experience in a Contract Research Organization (CRO) or Contract Manufacturing Organization (CMO) is preferred, but not required. Must have working knowledge of MS Office products, especially MS Project. Independence/Accountability: Must be a self-starter, self-motivated, and highly flexible in this home-based position with 25% travel. Must be organized and detail-oriented. Problem Solving: Proven experience creating and carrying out successful plans and processes to solve complex problems. Leadership Activities: Work closely with team members across all CMC-related business units and with the STA management team to ensure coordination of all efforts and real-time communication with all stakeholders. Communication Skills: Proficiency in English is required. Mandarin is a plus Excellent communication skills (verbal, written, and presentation skills).
Research Scientist - Formulation and Lyophilization
FUJIFILM Holdings America Corporation Warminster, Wiltshire
Position Overview We are hiring a Research Scientist - Formulation and Lyophilization. The Research Scientist - Formulation and Lyophilization will be responsible for leading formulation development studies to improve solubility, stability, and bioactivity of recombinant cytokines and growth factors, design and execute lyophilization cycles with a focus on reducing moisture content, improving cake appearance, and maintaining activity. They will evaluate excipients and delivery system compatibility for liquid and lyophilized formats (vials, bags, etc.), and provide scientific guidance to junior team members and support troubleshooting of formulation-related challenges. Company Overview FUJIFILM Irvine Scientific, Inc. is a global leader in the innovation and manufacture of cell culture solutions for Life Science and Medical markets, providing products and services that assistcustomers in advancing healthcare initiatives. Working across discovery research, cell and gene therapy, reproductive medicineand cytogenetics, as well as the large-scale production of biotherapeutics and vaccines, the Company istrusted by researchers, manufacturers, and cliniciansworldwide.For over 50 years, FUJIFILM Irvine Scientific'sMission has been to empower all who bring medicines and treatments to life with unmatched quality and responsiveness in itsproducts and custom solutions, providing customers with the vital resources needed to enrich human lives through innovative, accessible therapies. The Company'sfacilities adhere to both ISO and FDA regulations, with manufacturing facilities that follow cGMP guidelines in the USA, Japan, and the Netherlands, and a media optimization centerin China. All sites prioritize strategies that adhere to the FUJIFILM Sustainability ValuePlan 2030 for sustainable growth. FUJIFILM Irvine Scientific, Inc. is a subsidiary of FUJIFILM Holdings America Corporation reporting to FUJIFILM Holdings Corporation. Job Description Responsibilities Lead formulation development studies to improve solubility, stability, and bioactivity of recombinant cytokines and growth factors. Work closely with downstream scientists Design and execute lyophilization cycles with a focus on reducing moisture content, improving cake appearance, and maintaining activity. Evaluate excipients and delivery system compatibility for liquid and lyophilized formats (vials, bags etc.). Author technical reports, batch records, and development protocols. Collaborate with analytical teams for stability studies and characterization. Support scale-up of formulation and lyophilization processes for pilot and GMP manufacturing. Present formulation data to cross-functional teams and contribute to regulatory documentation. Provide scientific guidance to junior team members and support troubleshooting of formulation-related challenges. Required Skills/Education B.S. with more than 8 years, M.S. with 3-5 years, or Ph.D. with less than 2 years of relevant working experience in Biochemistry, Pharmaceutical Sciences, or a related field. Relevant work experience with proteins and purification techniques are required. Able to troubleshoot equipment and experimental problems independently. Perform advanced data analysis, use of statistical software and generate summary data reports & presentations (creation understandable graphical representations of data). Able to prepare formal reports and presentations independently with review/ very minor edits from supervisor. Able to interpret scientific literature, apply knowledge to projects (e.g. experimental design information, concentration ranges, etc.), use information to develop new and novel ideas/concepts/product development. Able to design scientifically sound experimental designs with minimal guidance. Strong experience in protein formulation development, particularly for biologics or therapeutic proteins. Proven hands-on experience with lyophilization cycle development and thermal characterization techniques. Familiarity with delivery system development for liquid and lyophilized formats Knowledge of protein stability, aggregation, and degradation pathways. Experience with analytical tools such as SEC-HPLC, DLS, UV, and CD preferred. Excellent data interpretation and scientific communication skills. General knowledge and application of project management skills. General understanding of the NPD/ phase gating process and function, able to apply this knowledge and support projects independently (i.e. completing check list items, participation in project timeline setting with other departments). Intermediate business acumen, learning/ understanding fundamental business concepts (i.e. general understanding of concepts and the ability to apply them to NPD). Desired Skills Strong understanding of the functions of other departments and able to work interdepartmentally/ cross functionally. Strong creative/ innovating thinking skills, intermediate level application of thoughts to process/ workflow improvements & product development. Actively participates in scientific discussion (e.g. meetings) demonstrating complex scientific/ critical thinking. Able to interact with upper management/ executive officers in a professional manner, expressing ideas and opinions clearly and concisely. Ability to speak, read and write English proficiently. Good oral and written communication skills Benefits Medical, Dental, Vision Life Insurance 401k Paid Time Off EEO Information Fujifilm is committedto providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc. ADA Information If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department ().
Jul 03, 2025
Full time
Position Overview We are hiring a Research Scientist - Formulation and Lyophilization. The Research Scientist - Formulation and Lyophilization will be responsible for leading formulation development studies to improve solubility, stability, and bioactivity of recombinant cytokines and growth factors, design and execute lyophilization cycles with a focus on reducing moisture content, improving cake appearance, and maintaining activity. They will evaluate excipients and delivery system compatibility for liquid and lyophilized formats (vials, bags, etc.), and provide scientific guidance to junior team members and support troubleshooting of formulation-related challenges. Company Overview FUJIFILM Irvine Scientific, Inc. is a global leader in the innovation and manufacture of cell culture solutions for Life Science and Medical markets, providing products and services that assistcustomers in advancing healthcare initiatives. Working across discovery research, cell and gene therapy, reproductive medicineand cytogenetics, as well as the large-scale production of biotherapeutics and vaccines, the Company istrusted by researchers, manufacturers, and cliniciansworldwide.For over 50 years, FUJIFILM Irvine Scientific'sMission has been to empower all who bring medicines and treatments to life with unmatched quality and responsiveness in itsproducts and custom solutions, providing customers with the vital resources needed to enrich human lives through innovative, accessible therapies. The Company'sfacilities adhere to both ISO and FDA regulations, with manufacturing facilities that follow cGMP guidelines in the USA, Japan, and the Netherlands, and a media optimization centerin China. All sites prioritize strategies that adhere to the FUJIFILM Sustainability ValuePlan 2030 for sustainable growth. FUJIFILM Irvine Scientific, Inc. is a subsidiary of FUJIFILM Holdings America Corporation reporting to FUJIFILM Holdings Corporation. Job Description Responsibilities Lead formulation development studies to improve solubility, stability, and bioactivity of recombinant cytokines and growth factors. Work closely with downstream scientists Design and execute lyophilization cycles with a focus on reducing moisture content, improving cake appearance, and maintaining activity. Evaluate excipients and delivery system compatibility for liquid and lyophilized formats (vials, bags etc.). Author technical reports, batch records, and development protocols. Collaborate with analytical teams for stability studies and characterization. Support scale-up of formulation and lyophilization processes for pilot and GMP manufacturing. Present formulation data to cross-functional teams and contribute to regulatory documentation. Provide scientific guidance to junior team members and support troubleshooting of formulation-related challenges. Required Skills/Education B.S. with more than 8 years, M.S. with 3-5 years, or Ph.D. with less than 2 years of relevant working experience in Biochemistry, Pharmaceutical Sciences, or a related field. Relevant work experience with proteins and purification techniques are required. Able to troubleshoot equipment and experimental problems independently. Perform advanced data analysis, use of statistical software and generate summary data reports & presentations (creation understandable graphical representations of data). Able to prepare formal reports and presentations independently with review/ very minor edits from supervisor. Able to interpret scientific literature, apply knowledge to projects (e.g. experimental design information, concentration ranges, etc.), use information to develop new and novel ideas/concepts/product development. Able to design scientifically sound experimental designs with minimal guidance. Strong experience in protein formulation development, particularly for biologics or therapeutic proteins. Proven hands-on experience with lyophilization cycle development and thermal characterization techniques. Familiarity with delivery system development for liquid and lyophilized formats Knowledge of protein stability, aggregation, and degradation pathways. Experience with analytical tools such as SEC-HPLC, DLS, UV, and CD preferred. Excellent data interpretation and scientific communication skills. General knowledge and application of project management skills. General understanding of the NPD/ phase gating process and function, able to apply this knowledge and support projects independently (i.e. completing check list items, participation in project timeline setting with other departments). Intermediate business acumen, learning/ understanding fundamental business concepts (i.e. general understanding of concepts and the ability to apply them to NPD). Desired Skills Strong understanding of the functions of other departments and able to work interdepartmentally/ cross functionally. Strong creative/ innovating thinking skills, intermediate level application of thoughts to process/ workflow improvements & product development. Actively participates in scientific discussion (e.g. meetings) demonstrating complex scientific/ critical thinking. Able to interact with upper management/ executive officers in a professional manner, expressing ideas and opinions clearly and concisely. Ability to speak, read and write English proficiently. Good oral and written communication skills Benefits Medical, Dental, Vision Life Insurance 401k Paid Time Off EEO Information Fujifilm is committedto providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc. ADA Information If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department ().
Principal Scientist
Griffith Foods Limited
Griffith Foods Ltd., Somercotes, Derbyshire, United Kingdom Job Description Posted Sunday, May 11, 2025 at 11:00 PM We blend care and creativity to nourish the world. Griffith Foods is global product development partner, we specialize in high-quality food ingredients. We serve global food companies and regional food companies worldwide. As a family business, we've valued people above all else for 100 years. Griffith is renowned for true, collaborative innovation. Our people care. We're committed to helping our customers create better products - and a better, more sustainable world. Learn more about Griffith Foods on The purpose of the role Executes R&D initiatives for the Product Category Team, with a primary focus on breakthrough and proactive innovation. Responsible for innovation project management. Enables product leadership in the product category to align with the overall business strategy and long-range plan. Provides technical expertise for the product category. Provides guidance and support to internal (regional) teams in relevant technical aspects for the product category. Responsibilities • Hands on Scientist with a passion to drive technical excellence, conduct innovative research, and independently plan, design, and execute experiments to develop disruptive solutions in alignment with innovation plan. • Responsible for the management, coordination and prioritization of the tasks, activities and duties of existing or future R&D Technicians or Technologists reporting into this role. • As part of the Innovation Process Management, understands and considers complex customer requirements across different regions (ingredients availability, product design, and legislative restrictions) as well as their operational processes and their technical requirements. • Leads the exploration, evaluation and implementation of new and novel ingredients and processing techniques at bench or commercial scale as needed. • Competent user of the Innovation Process Management system (IPM). • Participates in global related technical taskforces in conjunction with Global R&D, Marketing, Culinary and Business Development. • Maintains GLP's, GMP's, and all required laboratory records, using electronic systems and written protocols, to ensure data integrity and compliance. • Ensures the security and confidentiality of all information regarding Griffith Innovation or Client product formulas and related data. Requirements • Minimum Education o BSc in Food Science, Food Technology, Food Chemistry, Chemistry or related science • Preferred Education: o MSc in Food or related Science • Minimum Experience o 10 years. • Preferred Experience: o >12 years. Working at Griffith Foods We are a caring family company where everyone has the opportunity to grow, follow their own personal Purpose and find fulfillment in their work. We support each other, demonstrate mutual respect and nourish people's well-being. We believe in doing the right thing, especially when it is hard to do and recognize that our success depends on our customers' success consequently, we work together, leveraging our skills, knowledge and ideas to create exceptional products and solutions. We value diversity at our company and celebrate our cultural and personal differences, knowing that together, we create a unique source of strength. All qualified applicants will receive consideration for employment without regard to race, colour, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, or age. If you need assistance or an accommodation due to disability you may contact us at Griffith Foods Ltd., Somercotes, Derbyshire, United Kingdom
Jul 03, 2025
Full time
Griffith Foods Ltd., Somercotes, Derbyshire, United Kingdom Job Description Posted Sunday, May 11, 2025 at 11:00 PM We blend care and creativity to nourish the world. Griffith Foods is global product development partner, we specialize in high-quality food ingredients. We serve global food companies and regional food companies worldwide. As a family business, we've valued people above all else for 100 years. Griffith is renowned for true, collaborative innovation. Our people care. We're committed to helping our customers create better products - and a better, more sustainable world. Learn more about Griffith Foods on The purpose of the role Executes R&D initiatives for the Product Category Team, with a primary focus on breakthrough and proactive innovation. Responsible for innovation project management. Enables product leadership in the product category to align with the overall business strategy and long-range plan. Provides technical expertise for the product category. Provides guidance and support to internal (regional) teams in relevant technical aspects for the product category. Responsibilities • Hands on Scientist with a passion to drive technical excellence, conduct innovative research, and independently plan, design, and execute experiments to develop disruptive solutions in alignment with innovation plan. • Responsible for the management, coordination and prioritization of the tasks, activities and duties of existing or future R&D Technicians or Technologists reporting into this role. • As part of the Innovation Process Management, understands and considers complex customer requirements across different regions (ingredients availability, product design, and legislative restrictions) as well as their operational processes and their technical requirements. • Leads the exploration, evaluation and implementation of new and novel ingredients and processing techniques at bench or commercial scale as needed. • Competent user of the Innovation Process Management system (IPM). • Participates in global related technical taskforces in conjunction with Global R&D, Marketing, Culinary and Business Development. • Maintains GLP's, GMP's, and all required laboratory records, using electronic systems and written protocols, to ensure data integrity and compliance. • Ensures the security and confidentiality of all information regarding Griffith Innovation or Client product formulas and related data. Requirements • Minimum Education o BSc in Food Science, Food Technology, Food Chemistry, Chemistry or related science • Preferred Education: o MSc in Food or related Science • Minimum Experience o 10 years. • Preferred Experience: o >12 years. Working at Griffith Foods We are a caring family company where everyone has the opportunity to grow, follow their own personal Purpose and find fulfillment in their work. We support each other, demonstrate mutual respect and nourish people's well-being. We believe in doing the right thing, especially when it is hard to do and recognize that our success depends on our customers' success consequently, we work together, leveraging our skills, knowledge and ideas to create exceptional products and solutions. We value diversity at our company and celebrate our cultural and personal differences, knowing that together, we create a unique source of strength. All qualified applicants will receive consideration for employment without regard to race, colour, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, or age. If you need assistance or an accommodation due to disability you may contact us at Griffith Foods Ltd., Somercotes, Derbyshire, United Kingdom
Postdoctoral Researcher
EURAXESS Czech Republic
Organisation/Company John Innes Centre Research Field Biological sciences " Biology Researcher Profile First Stage Researcher (R1) Positions PhD Positions Country United Kingdom Application Deadline 2 Aug 2025 - 23:59 (Europe/London) Type of Contract Temporary Job Status Full-time Hours Per Week 37 Is the job funded through the EU Research Framework Programme? Not funded by a EU programme Is the Job related to staff position within a Research Infrastructure? No Offer Description An exciting opportunity has arisen for a Postdoctoral Researcher to join the Howard Group at the John Innes Centre, working on cutting-edge science in the field of Computational and Systems Biology. About the John Innes Centre: The John Innes Centre is an independent, international centre of excellence in plant and microbial sciences. We nurture a creative, curiosity-led approach to answering fundamental questions in bioscience, and translate that knowledge into societal benefits. Our strategic vision, Healthy Plants, Healthy People, Healthy Planet , sets out our ambitious long-term goals for the game changing impact of our science globally. Our employees enjoy access to state-of-the-art technology and a diverse range of specialist training opportunities, including support for leadership and management. Click here to find out more about working at the John Innes Centre. About the Howard Group: The Howard group combines simple, predictive mathematical and biophysical modelling with long-lasting experimental collaborations to dissect biological mechanisms too complex to unravel by experiments alone. In many cases we are able to rationalise complex biological dynamics into simple underlying mechanisms, with few components and interactions. Our approach is highly interdisciplinary and relies heavily on the techniques of statistical physics and applied mathematics, as well as on close collaboration with experimental groups. At present there are two main research areas in the group: probing how epigenetic memory states are set up and then stably maintained, and understanding patterning dynamics in sub-cellular biological systems. For epigenetics, we work on both histone modification memory systems, particularly the Polycomb silencing system, as well as on DNA methylation. For patterning, the main application at present is to the dynamics of crossover positioning in meiosis. The group regularly publishes in the most prominent multidisciplinary journals, with recent papers in Nature, Science, Cell Systems, eLife, Molecular Cell and PNAS. Several previous members of the Howard group now hold independent faculty positions of their own, including in Warwick, Glasgow, Sydney, Amsterdam and Munich. The role: The main purpose of the position is to develop predictive computational models of epigenetic dynamics, collaborating particularly with the experimental group of Prof Rob Klose in the Dept of Biochemistry, Oxford University. The models will enhance our understanding of how the Polycomb system silences gene expression and how such a silenced memory state can be stably maintained through many cell cycles. Theposition is funded by Wellcome and would suit an individual with a high degree of independence and vision, able to advance the project independently. The successful candidate will have a rare opportunity to work on fundamental biological processes in a truly interdisciplinary environment, with seamless collaboration with a leading experimental group. The ideal candidate: The ideal candidate will possess (or soon complete) a PhD in Theoretical Physics, Bio-Mathematics or Computational Biology. They will possess a strong interest in biological problems and have achieved demonstrable scientific success in previous roles. Prior experience of biological modelling is desirable but not essential. Additional information: This role meets the criteria for a visa application, and we encourage all qualified candidates to apply. Where the successful applicant requires a visa, we will fund the costs for their visa and the Immigration Health Surcharge. Please contact the Human Resources Team if you have any questions regarding your application or visa options. We are an equal opportunities employer, actively supporting inclusivity and diversity. As a Disability Confident organisation, we guarantee to offer an interview to all disabled applicants who meet the essential criteria for this vacancy. We are proud to hold a prestigious Gold Athena SWAN award in recognition of our inclusive culture, commitment and good practices towards advancing of gender equality. We offer an exciting, stimulating, diverse research environment and actively promote a family friendly workplace. The Institute is also a member of Stonewall's Diversity Champions programme. The John Innes Centre is a registered charity (No. 223852) grant-aided by the Biotechnology and Biological Sciences Research Council.
Jul 03, 2025
Full time
Organisation/Company John Innes Centre Research Field Biological sciences " Biology Researcher Profile First Stage Researcher (R1) Positions PhD Positions Country United Kingdom Application Deadline 2 Aug 2025 - 23:59 (Europe/London) Type of Contract Temporary Job Status Full-time Hours Per Week 37 Is the job funded through the EU Research Framework Programme? Not funded by a EU programme Is the Job related to staff position within a Research Infrastructure? No Offer Description An exciting opportunity has arisen for a Postdoctoral Researcher to join the Howard Group at the John Innes Centre, working on cutting-edge science in the field of Computational and Systems Biology. About the John Innes Centre: The John Innes Centre is an independent, international centre of excellence in plant and microbial sciences. We nurture a creative, curiosity-led approach to answering fundamental questions in bioscience, and translate that knowledge into societal benefits. Our strategic vision, Healthy Plants, Healthy People, Healthy Planet , sets out our ambitious long-term goals for the game changing impact of our science globally. Our employees enjoy access to state-of-the-art technology and a diverse range of specialist training opportunities, including support for leadership and management. Click here to find out more about working at the John Innes Centre. About the Howard Group: The Howard group combines simple, predictive mathematical and biophysical modelling with long-lasting experimental collaborations to dissect biological mechanisms too complex to unravel by experiments alone. In many cases we are able to rationalise complex biological dynamics into simple underlying mechanisms, with few components and interactions. Our approach is highly interdisciplinary and relies heavily on the techniques of statistical physics and applied mathematics, as well as on close collaboration with experimental groups. At present there are two main research areas in the group: probing how epigenetic memory states are set up and then stably maintained, and understanding patterning dynamics in sub-cellular biological systems. For epigenetics, we work on both histone modification memory systems, particularly the Polycomb silencing system, as well as on DNA methylation. For patterning, the main application at present is to the dynamics of crossover positioning in meiosis. The group regularly publishes in the most prominent multidisciplinary journals, with recent papers in Nature, Science, Cell Systems, eLife, Molecular Cell and PNAS. Several previous members of the Howard group now hold independent faculty positions of their own, including in Warwick, Glasgow, Sydney, Amsterdam and Munich. The role: The main purpose of the position is to develop predictive computational models of epigenetic dynamics, collaborating particularly with the experimental group of Prof Rob Klose in the Dept of Biochemistry, Oxford University. The models will enhance our understanding of how the Polycomb system silences gene expression and how such a silenced memory state can be stably maintained through many cell cycles. Theposition is funded by Wellcome and would suit an individual with a high degree of independence and vision, able to advance the project independently. The successful candidate will have a rare opportunity to work on fundamental biological processes in a truly interdisciplinary environment, with seamless collaboration with a leading experimental group. The ideal candidate: The ideal candidate will possess (or soon complete) a PhD in Theoretical Physics, Bio-Mathematics or Computational Biology. They will possess a strong interest in biological problems and have achieved demonstrable scientific success in previous roles. Prior experience of biological modelling is desirable but not essential. Additional information: This role meets the criteria for a visa application, and we encourage all qualified candidates to apply. Where the successful applicant requires a visa, we will fund the costs for their visa and the Immigration Health Surcharge. Please contact the Human Resources Team if you have any questions regarding your application or visa options. We are an equal opportunities employer, actively supporting inclusivity and diversity. As a Disability Confident organisation, we guarantee to offer an interview to all disabled applicants who meet the essential criteria for this vacancy. We are proud to hold a prestigious Gold Athena SWAN award in recognition of our inclusive culture, commitment and good practices towards advancing of gender equality. We offer an exciting, stimulating, diverse research environment and actively promote a family friendly workplace. The Institute is also a member of Stonewall's Diversity Champions programme. The John Innes Centre is a registered charity (No. 223852) grant-aided by the Biotechnology and Biological Sciences Research Council.
Structural Bioinformatics Lead Scientist
Lonza Group Ltd. Cambridge, Cambridgeshire
Structural Bioinformatics Lead Scientist Apply locations UK - Cambridge time type Full time posted on Posted Today job requisition id R67018 Today Lonza is a global leader in life sciences. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of. We are seeking a highly motivated and skilled Lead Scientist with experience in Structure-based Protein Engineering and Bioinformatics to join Lonza's EDS Bioinformatics team based in Cambridge, UK. Key responsibilities: The successful candidate will work on multiple customer projects focusing on in silico assessments and providing computational design for Antibody based & recombinant protein therapeutics. You will utilise our proprietary platforms for antibody humanisation and deimmunisation, immunogenicity (Epibase) and manufacturability risk assessments to improve the developability of potential bio-therapeutics of customers ranging from small biotech to big pharma. Additionally, you will contribute to the development of innovative technologies to support companies in their R&D programs and optimize proteins for the manufacturing processes. Key requirements: PhD or equivalent experience in Computational Chemistry, Structural Biology, Physics or Structural Bioinformatics preferably with proven experience. Highly experienced in protein structural analysis with emphasis on homology modeling and protein structure-based design. Strong understanding of molecular interactions is essential. Experienced working in Linux environment and scripting (knowledge of Python is essential). Experience in designing/developing ADCs would be an advantage. Ability to generate high quality reports and promote effective communication with the customer. Advanced analytical and critical problem-solving skills, combined with scientific creativity. Interest in continuous improvements of processes by integrating innovative solutions. Ability to work as a team member, as well as independently with minimal direction. Fluency in written and oral English, and strong written and oral communication skills. We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, colour, national origin, sex, gender, gender expression, sexual orientation, age, marital status, veteran status, or disability status. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. Every day, Lonza's products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically. People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.
Jul 03, 2025
Full time
Structural Bioinformatics Lead Scientist Apply locations UK - Cambridge time type Full time posted on Posted Today job requisition id R67018 Today Lonza is a global leader in life sciences. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of. We are seeking a highly motivated and skilled Lead Scientist with experience in Structure-based Protein Engineering and Bioinformatics to join Lonza's EDS Bioinformatics team based in Cambridge, UK. Key responsibilities: The successful candidate will work on multiple customer projects focusing on in silico assessments and providing computational design for Antibody based & recombinant protein therapeutics. You will utilise our proprietary platforms for antibody humanisation and deimmunisation, immunogenicity (Epibase) and manufacturability risk assessments to improve the developability of potential bio-therapeutics of customers ranging from small biotech to big pharma. Additionally, you will contribute to the development of innovative technologies to support companies in their R&D programs and optimize proteins for the manufacturing processes. Key requirements: PhD or equivalent experience in Computational Chemistry, Structural Biology, Physics or Structural Bioinformatics preferably with proven experience. Highly experienced in protein structural analysis with emphasis on homology modeling and protein structure-based design. Strong understanding of molecular interactions is essential. Experienced working in Linux environment and scripting (knowledge of Python is essential). Experience in designing/developing ADCs would be an advantage. Ability to generate high quality reports and promote effective communication with the customer. Advanced analytical and critical problem-solving skills, combined with scientific creativity. Interest in continuous improvements of processes by integrating innovative solutions. Ability to work as a team member, as well as independently with minimal direction. Fluency in written and oral English, and strong written and oral communication skills. We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, colour, national origin, sex, gender, gender expression, sexual orientation, age, marital status, veteran status, or disability status. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. Every day, Lonza's products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically. People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.
Scientific Associate 1
Charles River Laboratories, Research Models and Services, Germany GmbH
For 75years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we'll help you build a career that you can feel passionate about. IMPORTANT: In order to be considered for this position, a resume/CV must be uploaded and submitted during the application process. Please make sure work history and education are added correctly. Job Summary We are currently seeking a Scientific Associate 1 within the department of Immunology, Bioanalysis & Biomarkers located at our site at Clearwater House in Riccarton, Edinburgh. This is a 12 month fixed term contract opportunity. The Immunology, Bioanalysis and Biomarker team consists of a dynamic group of approximately 80 researchers that support our clients as they endeavour to bring novel treatments coving a wide range of therapeutic areas to patients. This multifunctional team ensures that clients are provided with accurate and reliable data in order to satisfy the regulatory expectations associated with bringing new treatments to the market. This is accomplished using a wide variety of scientific techniques across the fields of Immunochemistry, Immunology, Cell Based Assays and Molecular Biology. The successful applicant will be involved in the development, validation, and implementation of immunoassays to support PK/TK and Biomarker assessments (including those considered Safety; Pharmacodynamic; Surrogate; Predictive/Prognostic; Monitoring and Susceptibility). Key responsibilities include, but are not limited to: • Processing of samples • Operation of state-of-the-art analytical equipment • Recording and reporting of data. Profile and Requirements We are looking for applicants with excellent organisational skills with an eye for detail and quality. In addition to the following skills and experience, the candidate should have a BSc or MSc degree in a relevant discipline with good understanding of Immunology and Cell biology or drug development. Specific criteria that you are required to meet include: • Strong team player with good communication skills • Interest in working with sophisticated laboratory equipment • Understanding of core laboratory skills and techniques • Ability to perform well and thrive in a high-pressure environment • Basic understanding of GLP and GCP The salary for this role is £27,951.22 per annum. Following initial training and onboarding at our site based in Elphinstone, Tranent, the successful candidate will be based at our site in Clearwater House, Riccarton. Profile and Requirements IMPORTANT: A resume is required to be considered for this position. If you have not uploaded your resume in your candidate profile, please return to upload field and attach your resume/CV. About Safety Assessment Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 120 investigational new drug (IND) programs are conducted in our Safety Assessment facilities. About Charles River Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients' clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market. With over 20,000 employees within 110 facilities in 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client's unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. At Charles River, we are passionate about our role in improving the quality of people's lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of 86% of the drugs approved by the FDA in 2021. At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to the principle of diversity and inclusion and work daily in this direction. For more information, please visit . 228714
Jul 03, 2025
Full time
For 75years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we'll help you build a career that you can feel passionate about. IMPORTANT: In order to be considered for this position, a resume/CV must be uploaded and submitted during the application process. Please make sure work history and education are added correctly. Job Summary We are currently seeking a Scientific Associate 1 within the department of Immunology, Bioanalysis & Biomarkers located at our site at Clearwater House in Riccarton, Edinburgh. This is a 12 month fixed term contract opportunity. The Immunology, Bioanalysis and Biomarker team consists of a dynamic group of approximately 80 researchers that support our clients as they endeavour to bring novel treatments coving a wide range of therapeutic areas to patients. This multifunctional team ensures that clients are provided with accurate and reliable data in order to satisfy the regulatory expectations associated with bringing new treatments to the market. This is accomplished using a wide variety of scientific techniques across the fields of Immunochemistry, Immunology, Cell Based Assays and Molecular Biology. The successful applicant will be involved in the development, validation, and implementation of immunoassays to support PK/TK and Biomarker assessments (including those considered Safety; Pharmacodynamic; Surrogate; Predictive/Prognostic; Monitoring and Susceptibility). Key responsibilities include, but are not limited to: • Processing of samples • Operation of state-of-the-art analytical equipment • Recording and reporting of data. Profile and Requirements We are looking for applicants with excellent organisational skills with an eye for detail and quality. In addition to the following skills and experience, the candidate should have a BSc or MSc degree in a relevant discipline with good understanding of Immunology and Cell biology or drug development. Specific criteria that you are required to meet include: • Strong team player with good communication skills • Interest in working with sophisticated laboratory equipment • Understanding of core laboratory skills and techniques • Ability to perform well and thrive in a high-pressure environment • Basic understanding of GLP and GCP The salary for this role is £27,951.22 per annum. Following initial training and onboarding at our site based in Elphinstone, Tranent, the successful candidate will be based at our site in Clearwater House, Riccarton. Profile and Requirements IMPORTANT: A resume is required to be considered for this position. If you have not uploaded your resume in your candidate profile, please return to upload field and attach your resume/CV. About Safety Assessment Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 120 investigational new drug (IND) programs are conducted in our Safety Assessment facilities. About Charles River Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients' clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market. With over 20,000 employees within 110 facilities in 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client's unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. At Charles River, we are passionate about our role in improving the quality of people's lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of 86% of the drugs approved by the FDA in 2021. At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to the principle of diversity and inclusion and work daily in this direction. For more information, please visit . 228714
Team Leader - Molecular Biology
Cpl Healthcare
Job Title: Team Leader - Molecular Biology Location: London Pay rate: Up to £50 per hour Contract Duration: 12-month contract Cpl Life Sciences is working exclusively with a biotech company committed to advancing human health and scientific discovery. They are seeking an accomplished Team Leader in Molecular Biology to drive cutting-edge research and innovation within their advanced biopharmaceutical division. This role is crucial in shaping and integrating strategies, guiding high-impact projects, and mentoring a team of industry-leading scientists. Key Responsibilities: Define and execute the molecular biology strategy, aligning with business goals to accelerate therapeutic development. Lead, mentor, and grow a high-performing team of scientists, fostering innovation, technical excellence, and career progression. Oversee the development and validation of novel molecular biology methodologies, ensuring scientific proficiency and industry-leading innovation. Drive automation, data-driven approaches, and next-generation sequencing (NGS) to enhance molecular biology capabilities. Work closely with departments including Bioinformatics, Process Development, and Clinical Research to drive integrated solutions. Ensure all molecular biology processes align with GMP, GLP, and regulatory expectations from the FDA, EMA, and other governing bodies. Represent the company in scientific conferences, regulatory discussions, and strategic partnerships to advance molecular research impact. Essential Skills & Experience: PhD in Molecular Biology, Biochemistry, Biotechnology, or a related field. Over 6-8 years of experience in molecular biology R&D, with a strong track record in senior roles within biotech or pharmaceutical organizations. Deep expertise in gene editing, synthetic biology, CRISPR, mRNA technology, plasmid DNA manufacturing, and cell-based assays. Experience in working within GMP/GLP-regulated environments and knowledge of global regulatory frameworks. Strong leadership and people management skills with experience building and leading large scientific teams. Proven ability to translate research into commercial and clinical applications. Excellent communication, stakeholder engagement, and project management skills. If you are interested, please apply now or send your CV to .
Jul 03, 2025
Full time
Job Title: Team Leader - Molecular Biology Location: London Pay rate: Up to £50 per hour Contract Duration: 12-month contract Cpl Life Sciences is working exclusively with a biotech company committed to advancing human health and scientific discovery. They are seeking an accomplished Team Leader in Molecular Biology to drive cutting-edge research and innovation within their advanced biopharmaceutical division. This role is crucial in shaping and integrating strategies, guiding high-impact projects, and mentoring a team of industry-leading scientists. Key Responsibilities: Define and execute the molecular biology strategy, aligning with business goals to accelerate therapeutic development. Lead, mentor, and grow a high-performing team of scientists, fostering innovation, technical excellence, and career progression. Oversee the development and validation of novel molecular biology methodologies, ensuring scientific proficiency and industry-leading innovation. Drive automation, data-driven approaches, and next-generation sequencing (NGS) to enhance molecular biology capabilities. Work closely with departments including Bioinformatics, Process Development, and Clinical Research to drive integrated solutions. Ensure all molecular biology processes align with GMP, GLP, and regulatory expectations from the FDA, EMA, and other governing bodies. Represent the company in scientific conferences, regulatory discussions, and strategic partnerships to advance molecular research impact. Essential Skills & Experience: PhD in Molecular Biology, Biochemistry, Biotechnology, or a related field. Over 6-8 years of experience in molecular biology R&D, with a strong track record in senior roles within biotech or pharmaceutical organizations. Deep expertise in gene editing, synthetic biology, CRISPR, mRNA technology, plasmid DNA manufacturing, and cell-based assays. Experience in working within GMP/GLP-regulated environments and knowledge of global regulatory frameworks. Strong leadership and people management skills with experience building and leading large scientific teams. Proven ability to translate research into commercial and clinical applications. Excellent communication, stakeholder engagement, and project management skills. If you are interested, please apply now or send your CV to .
Principal Scientist I - Protein Analysis
Syngenta AG
We are seeking a highly skilled and independent proteomics expert to join our Bioscience Crop Protection R&D function at Syngenta. This critical role is required to deliver multidisciplinary collaborative work programmes linked to lead discovery and safer-by-design initiatives within our Target Identification group. The successful candidate will leverage advanced proteomic techniques (including activity-based protein profiling, affinity-based methods, stability-based proteome profiling) to drive target identification and characterisation, which are essential for the development of innovative pest control solutions and enhance our understanding of molecular toxicological mechanisms to improve assessments of human safety. Responsibilities will include the implementation and optimisation of these techniques, managing complex proteomic data analysis and fostering strong collaboration across multi-disciplinary teams. Company Description Syngenta is a leading science based ag-tech company helping to improve global food security by enabling millions of farmers to make better use of available resources. Through world class science and innovative crop solutions, our 30,000 people in over 100 countries are working to transform how crops are grown.We are committed to rescuing land from degradation, enhancing biodiversity and revitalizing rural communities. Syngenta Crop Protection is a leader in agricultural innovation, bringing breakthrough technologies and solutions that enable farmers to grow healthy and nutritious food while taking care of the planet. We offer a leading portfolio of crop protection solutions for plant and soil health, as well as digital solutions that transform the decision-making capabilities of farmers. Our 17,900 employees serve to advance agriculture in more than 90 countries around the world. Syngenta Crop Protection is headquartered in Basel, Switzerland, and is part of the Syngenta Group. Our employees reflect the diversity of our customers, the markets where we operate and the communities which we serve. Regardless of your position, you will have a vital role in safely feeding an ever-increasing population while taking care of our planet. Join us and help shape the future of agriculture. Qualifications What are we looking for? Ph.D. in Proteomics, Biochemistry, Molecular biology, or a related field. Extensive experience with quantitative mass spectrometry-based proteomic workflows and technologies to understand complex biological questions in the domains of target identification and toxicology. Proficiency in bioinformatics and statistical tools to process and interpret quantitative proteomic data, identifying trends, patterns, and meaningful biological insights. Hands on experience of instrument set-up and data-acquisition. Ability and desire to work as part of a team and to work without technical supervision. Experience mentoring and training scientific colleagues in proteomic methodologies and data analysis Strong critical thinking and communication skills for collaboration and reporting. Additional Information Our site Jealott's Hill International Research Centre UK is situated in pleasant semi-rural surroundings between Bracknell and Maidenhead and is the place of work for approximately 800 Syngenta scientists and support staff. Jealott's Hill is one of the main global research and development sites and key activities include research into discovery of new active ingredients, new formulation technologies, product safety and technical support of our product range. What we offer Extensive benefits package including a generous pension scheme, bonus scheme, private medical & life insurance. Up to 31.5 days annual holiday. The chance to work as part of a team to address the current and future needs of the agricultural sector and help feed an ever-increasing population. A vibrant growth and learning culture and wide range of training options. We offer a position which contributes to valuable and impactful work in a stimulating and international environment. An open, supportive, and collaborative working culture. Syngenta has been ranked as a top 5 employer and number 1 in agriculture by Science Journal. Syngenta is an Equal Opportunity Employer and does not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. Learn more about our D&I initiatives here: Jealott's Hill has Disability Confident certification. We are committed to making all stages of our recruitment process accessible to all candidates and our Jealott's Hill site are a Disability Confident Level 2 Employer. Please let us know if you need any assistance or reasonable adjustments throughout your application and we will do everything we can to support you.
Jul 03, 2025
Full time
We are seeking a highly skilled and independent proteomics expert to join our Bioscience Crop Protection R&D function at Syngenta. This critical role is required to deliver multidisciplinary collaborative work programmes linked to lead discovery and safer-by-design initiatives within our Target Identification group. The successful candidate will leverage advanced proteomic techniques (including activity-based protein profiling, affinity-based methods, stability-based proteome profiling) to drive target identification and characterisation, which are essential for the development of innovative pest control solutions and enhance our understanding of molecular toxicological mechanisms to improve assessments of human safety. Responsibilities will include the implementation and optimisation of these techniques, managing complex proteomic data analysis and fostering strong collaboration across multi-disciplinary teams. Company Description Syngenta is a leading science based ag-tech company helping to improve global food security by enabling millions of farmers to make better use of available resources. Through world class science and innovative crop solutions, our 30,000 people in over 100 countries are working to transform how crops are grown.We are committed to rescuing land from degradation, enhancing biodiversity and revitalizing rural communities. Syngenta Crop Protection is a leader in agricultural innovation, bringing breakthrough technologies and solutions that enable farmers to grow healthy and nutritious food while taking care of the planet. We offer a leading portfolio of crop protection solutions for plant and soil health, as well as digital solutions that transform the decision-making capabilities of farmers. Our 17,900 employees serve to advance agriculture in more than 90 countries around the world. Syngenta Crop Protection is headquartered in Basel, Switzerland, and is part of the Syngenta Group. Our employees reflect the diversity of our customers, the markets where we operate and the communities which we serve. Regardless of your position, you will have a vital role in safely feeding an ever-increasing population while taking care of our planet. Join us and help shape the future of agriculture. Qualifications What are we looking for? Ph.D. in Proteomics, Biochemistry, Molecular biology, or a related field. Extensive experience with quantitative mass spectrometry-based proteomic workflows and technologies to understand complex biological questions in the domains of target identification and toxicology. Proficiency in bioinformatics and statistical tools to process and interpret quantitative proteomic data, identifying trends, patterns, and meaningful biological insights. Hands on experience of instrument set-up and data-acquisition. Ability and desire to work as part of a team and to work without technical supervision. Experience mentoring and training scientific colleagues in proteomic methodologies and data analysis Strong critical thinking and communication skills for collaboration and reporting. Additional Information Our site Jealott's Hill International Research Centre UK is situated in pleasant semi-rural surroundings between Bracknell and Maidenhead and is the place of work for approximately 800 Syngenta scientists and support staff. Jealott's Hill is one of the main global research and development sites and key activities include research into discovery of new active ingredients, new formulation technologies, product safety and technical support of our product range. What we offer Extensive benefits package including a generous pension scheme, bonus scheme, private medical & life insurance. Up to 31.5 days annual holiday. The chance to work as part of a team to address the current and future needs of the agricultural sector and help feed an ever-increasing population. A vibrant growth and learning culture and wide range of training options. We offer a position which contributes to valuable and impactful work in a stimulating and international environment. An open, supportive, and collaborative working culture. Syngenta has been ranked as a top 5 employer and number 1 in agriculture by Science Journal. Syngenta is an Equal Opportunity Employer and does not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. Learn more about our D&I initiatives here: Jealott's Hill has Disability Confident certification. We are committed to making all stages of our recruitment process accessible to all candidates and our Jealott's Hill site are a Disability Confident Level 2 Employer. Please let us know if you need any assistance or reasonable adjustments throughout your application and we will do everything we can to support you.
Principal Scientist - Biokinetics
Syngenta AG
About the role We have an exciting opportunity for a a talented and versatile Principal Scientist to join our Bioperformance group opportunity to grow and lead in a dynamic, matrix organization focused on developing innovative insecticides. You will not only contribute your scientific expertise but also play a crucial leadership role, while being responsible for managing and developing team members, setting priorities, providing feedback, and offering development coaching. Key responsibilities will include: Leading and contributing to various stages of the insecticide discovery pipeline, with a focus on enhancing the Bioperformance profile of insect control products. Fostering a positive team culture that prioritizes HSE, effective data management, and innovative thinking in insect control research. Applying entomological knowledge to develop and optimize novel insecticides, considering insect biology, behaviour, and resistance mechanisms. Develop expertise in ADME (Absorption, Distribution, Metabolism, and Excretion) and metabolism studies, focusing on understanding the pharmacokinetics and metabolism of novel insecticides in target insects, beneficial insects, plants, and other relevant matrices to improve biological performance. Design and conduct bioassays to evaluate the efficacy of potential insecticides against various insect pests, including resistant populations. Collaborating with analytical teams on method development for insecticide detection and quantification in various samples, and interpret complex data to optimize insecticide candidates for enhanced Bioperformance. Working within a matrix structure, managing multiple projects and reporting lines, while fostering collaboration with cross-functional teams to achieve insect control research goals. Company Description Syngenta Crop Protection is a leader in agricultural innovation, bringing breakthrough technologies and solutions that enable farmers to grow healthy and nutritious food while taking care of the planet. We offer a leading portfolio of crop protection solutions for plant and soil health, as well as digital solutions that transform the decision-making capabilities of farmers. Our 17,900 employees serve to advance agriculture in more than 90 countries around the world. Syngenta Crop Protection is headquartered in Basel, Switzerland, and is part of the Syngenta Group. Our employees reflect the diversity of our customers, the markets where we operate and the communities which we serve. Regardless of your position, you will have a vital role in safely feeding an ever-increasing population while taking care of our planet. Join us and help shape the future of agriculture. Qualifications What we are looking for? Ph.D. in Entomology, Agricultural Sciences, Biology, Biochemistry, Chemistry, or a related field relevant to insect control research and Bioperformance. Extensive experience in insecticide research or a related field, with the ability to manage and develop team members, while fostering a positive team culture. Strong understanding of insect biology, physiology, and behaviour, as well as crop protection discovery pipelines and factors influencing insecticide bioperformance. Experience in designing and conducting insect bioassays and interpreting results. Proven track record of scientific publications and presentations in fields related to entomology, insect control, and bioperformance. Proficiency in data analysis and interpretation, with experience in using relevant software tools. Proven ability to thrive in a matrix organization, managing multiple insecticide discovery projects, with the ability to influence across diverse functional areas. Desired skills Experience with analytical techniques such as LC-MS/MS or HPLC. Familiarity with ADME concepts and their application in insecticide research and Bioperformance optimization. Experience in studies involving multiple biological matrices (e.g., insects, plants, soil, mammals) relevant to insecticide development. Knowledge of insecticide modes of action, resistance mechanisms, environmental fate, and factors affecting Bioperformance. Familiarity with computational tools, modelling techniques and the mindset to enable them. Strong project management skills and ability to navigate complex organizational structures in the context of insecticide development programs. Additional Information Our site Jealott's Hill International Research Centre UK is situated in pleasant semi-rural surroundings between Bracknell and Maidenhead and is the place of work for approximately 800 Syngenta scientists and support staff. Jealott's Hill is one of the main global research and development sites and key activities include research into discovery of new active ingredients, new formulation technologies, product safety and technical support of our product range. What we offer Extensive benefits package including a generous pension scheme, bonus scheme, private medical & life insurance. Up to 31.5 days annual holiday. We offer a position which contributes to valuable and impactful work in a stimulating and international environment. The chance to work as part of a global team to address the current and future needs of the agricultural sector and help feed an ever-increasing population. A vibrant growth and learning culture and wide range of training options. Syngenta has been ranked as a top 5 employer and number 1 in agriculture by Science Journal. Syngenta is an Equal Opportunity Employer and does not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. Learn more about our D&I initiatives here: Jealott's Hill has Disability Confident certification. We are committed to making all stages of our recruitment process accessible to all candidates and our Jealott's Hill site are a Disability Confident Level 2 Employer. Please let us know if you need any assistance or reasonable adjustments throughout your application and we will do everything we can to support you.
Jul 03, 2025
Full time
About the role We have an exciting opportunity for a a talented and versatile Principal Scientist to join our Bioperformance group opportunity to grow and lead in a dynamic, matrix organization focused on developing innovative insecticides. You will not only contribute your scientific expertise but also play a crucial leadership role, while being responsible for managing and developing team members, setting priorities, providing feedback, and offering development coaching. Key responsibilities will include: Leading and contributing to various stages of the insecticide discovery pipeline, with a focus on enhancing the Bioperformance profile of insect control products. Fostering a positive team culture that prioritizes HSE, effective data management, and innovative thinking in insect control research. Applying entomological knowledge to develop and optimize novel insecticides, considering insect biology, behaviour, and resistance mechanisms. Develop expertise in ADME (Absorption, Distribution, Metabolism, and Excretion) and metabolism studies, focusing on understanding the pharmacokinetics and metabolism of novel insecticides in target insects, beneficial insects, plants, and other relevant matrices to improve biological performance. Design and conduct bioassays to evaluate the efficacy of potential insecticides against various insect pests, including resistant populations. Collaborating with analytical teams on method development for insecticide detection and quantification in various samples, and interpret complex data to optimize insecticide candidates for enhanced Bioperformance. Working within a matrix structure, managing multiple projects and reporting lines, while fostering collaboration with cross-functional teams to achieve insect control research goals. Company Description Syngenta Crop Protection is a leader in agricultural innovation, bringing breakthrough technologies and solutions that enable farmers to grow healthy and nutritious food while taking care of the planet. We offer a leading portfolio of crop protection solutions for plant and soil health, as well as digital solutions that transform the decision-making capabilities of farmers. Our 17,900 employees serve to advance agriculture in more than 90 countries around the world. Syngenta Crop Protection is headquartered in Basel, Switzerland, and is part of the Syngenta Group. Our employees reflect the diversity of our customers, the markets where we operate and the communities which we serve. Regardless of your position, you will have a vital role in safely feeding an ever-increasing population while taking care of our planet. Join us and help shape the future of agriculture. Qualifications What we are looking for? Ph.D. in Entomology, Agricultural Sciences, Biology, Biochemistry, Chemistry, or a related field relevant to insect control research and Bioperformance. Extensive experience in insecticide research or a related field, with the ability to manage and develop team members, while fostering a positive team culture. Strong understanding of insect biology, physiology, and behaviour, as well as crop protection discovery pipelines and factors influencing insecticide bioperformance. Experience in designing and conducting insect bioassays and interpreting results. Proven track record of scientific publications and presentations in fields related to entomology, insect control, and bioperformance. Proficiency in data analysis and interpretation, with experience in using relevant software tools. Proven ability to thrive in a matrix organization, managing multiple insecticide discovery projects, with the ability to influence across diverse functional areas. Desired skills Experience with analytical techniques such as LC-MS/MS or HPLC. Familiarity with ADME concepts and their application in insecticide research and Bioperformance optimization. Experience in studies involving multiple biological matrices (e.g., insects, plants, soil, mammals) relevant to insecticide development. Knowledge of insecticide modes of action, resistance mechanisms, environmental fate, and factors affecting Bioperformance. Familiarity with computational tools, modelling techniques and the mindset to enable them. Strong project management skills and ability to navigate complex organizational structures in the context of insecticide development programs. Additional Information Our site Jealott's Hill International Research Centre UK is situated in pleasant semi-rural surroundings between Bracknell and Maidenhead and is the place of work for approximately 800 Syngenta scientists and support staff. Jealott's Hill is one of the main global research and development sites and key activities include research into discovery of new active ingredients, new formulation technologies, product safety and technical support of our product range. What we offer Extensive benefits package including a generous pension scheme, bonus scheme, private medical & life insurance. Up to 31.5 days annual holiday. We offer a position which contributes to valuable and impactful work in a stimulating and international environment. The chance to work as part of a global team to address the current and future needs of the agricultural sector and help feed an ever-increasing population. A vibrant growth and learning culture and wide range of training options. Syngenta has been ranked as a top 5 employer and number 1 in agriculture by Science Journal. Syngenta is an Equal Opportunity Employer and does not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. Learn more about our D&I initiatives here: Jealott's Hill has Disability Confident certification. We are committed to making all stages of our recruitment process accessible to all candidates and our Jealott's Hill site are a Disability Confident Level 2 Employer. Please let us know if you need any assistance or reasonable adjustments throughout your application and we will do everything we can to support you.
DataAnnotation
Research Scientist (Chemistry) - AI Trainer
DataAnnotation Wakefield, Yorkshire
We are looking for an advanced chemist to join our team to train AI models. You will measure the progress of these AI chatbots, evaluate their logic, and solve problems to improve the quality of each model. In this role you will need to hold an expert understanding of chemistry- a completed or in progress Masters/PhD is preferred but not required. Other related fields include, but are not limited to: Formulation Scientist, Development Chemist, Analytical Chemist, Chemical Engineer, Medicinal Chemist, Biochemist, Process Development Chemist. Benefits: This is a full-time or part-time REMOTE position You'll be able to choose which projects you want to work on You can work on your own schedule Projects are paid hourly starting at $40+ USD per hour, with bonuses on high-quality and high-volume work Responsibilities: Give AI chatbots diverse and complex chemistry problems and evaluate their outputs Evaluate the quality produced by AI models for correctness and performance Qualifications: A current, in progress, or completed Masters and/or PhD is preferred but not required Fluency in English (native or bilingual level) Detail-oriented Proficient in chemistry and inductive/deductive reasoning, physical/temporal/ spatial reasoning Note: Payment is made via PayPal. We will never ask for any money from you. PayPal will handle any currency conversions from USD. Job Types: Full-time, Part-time Pay: From £29.06 per hour Work Location: Remote
Jul 03, 2025
Full time
We are looking for an advanced chemist to join our team to train AI models. You will measure the progress of these AI chatbots, evaluate their logic, and solve problems to improve the quality of each model. In this role you will need to hold an expert understanding of chemistry- a completed or in progress Masters/PhD is preferred but not required. Other related fields include, but are not limited to: Formulation Scientist, Development Chemist, Analytical Chemist, Chemical Engineer, Medicinal Chemist, Biochemist, Process Development Chemist. Benefits: This is a full-time or part-time REMOTE position You'll be able to choose which projects you want to work on You can work on your own schedule Projects are paid hourly starting at $40+ USD per hour, with bonuses on high-quality and high-volume work Responsibilities: Give AI chatbots diverse and complex chemistry problems and evaluate their outputs Evaluate the quality produced by AI models for correctness and performance Qualifications: A current, in progress, or completed Masters and/or PhD is preferred but not required Fluency in English (native or bilingual level) Detail-oriented Proficient in chemistry and inductive/deductive reasoning, physical/temporal/ spatial reasoning Note: Payment is made via PayPal. We will never ask for any money from you. PayPal will handle any currency conversions from USD. Job Types: Full-time, Part-time Pay: From £29.06 per hour Work Location: Remote
DataAnnotation
Process Development Chemist - AI Trainer
DataAnnotation Edinburgh, Midlothian
We are looking for an advanced chemist to join our team to train AI models. You will measure the progress of these AI chatbots, evaluate their logic, and solve problems to improve the quality of each model. In this role you will need to hold an expert understanding of chemistry- a completed or in progress Masters/PhD is preferred but not required. Other related fields include, but are not limited to: Formulation Scientist, Development Chemist, Analytical Chemist, Chemical Engineer, Medicinal Chemist, Biochemist, Process Development Chemist. Benefits: This is a full-time or part-time REMOTE position You'll be able to choose which projects you want to work on You can work on your own schedule Projects are paid hourly starting at $40+ USD per hour, with bonuses on high-quality and high-volume work Responsibilities: Give AI chatbots diverse and complex chemistry problems and evaluate their outputs Evaluate the quality produced by AI models for correctness and performance Qualifications: A current, in progress, or completed Masters and/or PhD is preferred but not required Fluency in English (native or bilingual level) Detail-oriented Proficient in chemistry and inductive/deductive reasoning, physical/temporal/ spatial reasoning Note: Payment is made via PayPal. We will never ask for any money from you. PayPal will handle any currency conversions from USD. Job Types: Full-time, Part-time Pay: From £29.06 per hour Expected hours: 1 - 40 per week Work Location: Remote
Jul 03, 2025
Full time
We are looking for an advanced chemist to join our team to train AI models. You will measure the progress of these AI chatbots, evaluate their logic, and solve problems to improve the quality of each model. In this role you will need to hold an expert understanding of chemistry- a completed or in progress Masters/PhD is preferred but not required. Other related fields include, but are not limited to: Formulation Scientist, Development Chemist, Analytical Chemist, Chemical Engineer, Medicinal Chemist, Biochemist, Process Development Chemist. Benefits: This is a full-time or part-time REMOTE position You'll be able to choose which projects you want to work on You can work on your own schedule Projects are paid hourly starting at $40+ USD per hour, with bonuses on high-quality and high-volume work Responsibilities: Give AI chatbots diverse and complex chemistry problems and evaluate their outputs Evaluate the quality produced by AI models for correctness and performance Qualifications: A current, in progress, or completed Masters and/or PhD is preferred but not required Fluency in English (native or bilingual level) Detail-oriented Proficient in chemistry and inductive/deductive reasoning, physical/temporal/ spatial reasoning Note: Payment is made via PayPal. We will never ask for any money from you. PayPal will handle any currency conversions from USD. Job Types: Full-time, Part-time Pay: From £29.06 per hour Expected hours: 1 - 40 per week Work Location: Remote
DataAnnotation
Content Developer (Chemistry) - AI Trainer
DataAnnotation Stoke-on-trent, Staffordshire
We are looking for an advanced chemist to join our team to train AI models. You will measure the progress of these AI chatbots, evaluate their logic, and solve problems to improve the quality of each model. In this role you will need to hold an expert understanding of chemistry- a completed or in progress Masters/PhD is preferred but not required. Other related fields include, but are not limited to: Formulation Scientist, Development Chemist, Analytical Chemist, Chemical Engineer, Medicinal Chemist, Biochemist, Process Development Chemist. Benefits: This is a full-time or part-time REMOTE position You'll be able to choose which projects you want to work on You can work on your own schedule Projects are paid hourly starting at $40+ USD per hour, with bonuses on high-quality and high-volume work Responsibilities: Give AI chatbots diverse and complex chemistry problems and evaluate their outputs Evaluate the quality produced by AI models for correctness and performance Qualifications: A current, in progress, or completed Masters and/or PhD is preferred but not required Fluency in English (native or bilingual level) Detail-oriented Proficient in chemistry and inductive/deductive reasoning, physical/temporal/ spatial reasoning Note: Payment is made via PayPal. We will never ask for any money from you. PayPal will handle any currency conversions from USD. Job Types: Full-time, Part-time Pay: From £29.06 per hour Work Location: Remote
Jul 03, 2025
Full time
We are looking for an advanced chemist to join our team to train AI models. You will measure the progress of these AI chatbots, evaluate their logic, and solve problems to improve the quality of each model. In this role you will need to hold an expert understanding of chemistry- a completed or in progress Masters/PhD is preferred but not required. Other related fields include, but are not limited to: Formulation Scientist, Development Chemist, Analytical Chemist, Chemical Engineer, Medicinal Chemist, Biochemist, Process Development Chemist. Benefits: This is a full-time or part-time REMOTE position You'll be able to choose which projects you want to work on You can work on your own schedule Projects are paid hourly starting at $40+ USD per hour, with bonuses on high-quality and high-volume work Responsibilities: Give AI chatbots diverse and complex chemistry problems and evaluate their outputs Evaluate the quality produced by AI models for correctness and performance Qualifications: A current, in progress, or completed Masters and/or PhD is preferred but not required Fluency in English (native or bilingual level) Detail-oriented Proficient in chemistry and inductive/deductive reasoning, physical/temporal/ spatial reasoning Note: Payment is made via PayPal. We will never ask for any money from you. PayPal will handle any currency conversions from USD. Job Types: Full-time, Part-time Pay: From £29.06 per hour Work Location: Remote
HAVAS
New Business and Marketing Manager
HAVAS
Agency : Havas Media Group Job Description : The Business Consultant is responsible for the day-to-day relationships management of a client portfolio and for the delivery of the (Mx) Media Experience services by facilitating the connection between Business client teams and Intelligence / Media Development / Measurement teams. The Havas Media Network Growth Team have been the driving force behind high profile pitch wins including Ocado, Abercrombie & Kent, ULaw and Red Bull, and several industry awards nominations and wins. We're a fast-paced, nurturing team looking for an ambitious new business and marketing manager to support the agency's growth function. The Role We are looking for an experienced New Business and Marketing Manager to join the Havas Media Growth team. This is a mid-level role, expected to create strong working relationships with employees across all levels, especially senior stakeholders. The new business and marketing manager should be highly organised and process-driven, with a clear desire to learn and progress. This person will be required to manage multiple workstreams and projects at one time, whilst continually maintaining a high work standard. They will be an excellent communicator, who values honesty, transparency and is able to ask for help. Necessary skills include the ability to display a positive attitude whilst under pressure, and successfully manage upwards to ensure workload to completed on time. They will have a keen desire, willingness and curiosity to learn about agency marketing, overall running of the business, the clients we work with, the capabilities we deliver and the wider industry. Staying abreast of new innovations, and competitors within the industry, to be able to contribute effectively to successful growth and running of the agencies. This is a great opportunity for someone with 2-5 years' experience in creative or media agencies, working in similar new business and marketing roles. Responsibilities The role has three primary areas of focus: Managing key New Biz opportunities through the full end-to-end process Delivering impactful, consistent marketing Collaborating with the wider growth function to deliver Havas Media's growth plan and ambition New Business Reviewing and sharing inbound opportunities with the New Business leadership team - New Business Director & Chief Growth Officer Support across all new business requirements such as pitch management, pitch theatre, RFI's, RFP's and creds decks Manage team communication / diarising / own research and prep / client profiles & background info Support New Business Director on all new business opportunities, including pitch management, pitch theatre, RFIs, Chemistry and Tissue meetings Tracking relevant new business external tender sites Ensure team processes and communications are run smoothly Organise and manage case study library and creation of assets Management of New Business & Marketing Team assets Marketing Own creation of marketing materials, inc management of content calendar, social, email campaigns - draft copy, plan ahead, evaluate (monthly report) Management of agency social channels, website and intermediary profiles Collaborating with the comms team to amplify our trade content Collaborate with the wider team on event management, including comms, logistics and evaluation Collaborating with strategy team on annual awards planning and entries Case study library and asset management Reporting/coordination Management and tracking of the new business pipeline and CRM reporting (agency, network and village level) Compiling competitor and industry reviews Completing ad hoc requests from the wider Havas Media Network We are looking for: Adaptability and the ability to juggle changing priorities Meticulously organised and with a keen eye for detail Natural collaborator A 'growth mindset' - hand-raising, listens to and incorporates feedback, keen to learn An individual who brings passion and energy to the team and is always looking for ways to improve what we do Someone who is accountable, reliable and honest Ability to work to tight deadlines and under pressure Demonstrable experience at senior executive/manager level in a new business, client or investment role Confidence to be able to deal with the most senior level stakeholders Strong writing skills are important Strong PowerPoint, Microsoft Outlook, Microsoft Teams, email marketing skills Havas Media Boilerplate We believe brands mean more by bringing them closer to people - and that's why our ambition is to be the most customer-centric media agency in the UK. With origins in 1987, we have decades of experience in giving a competitive edge to the likes of Domino's, British Red Cross, Homebase, Starbucks, BBC, KIA, Hyundai, Dreams and EDF, building people-first media experiences from deep audience insights and curated data threads - all backed by the scale and data power of Havas Media Network UK. Havas is an equal opportunities employer and welcomes everyone to our team. We strongly encourage people of colour, lesbian, gay, bisexual, transgender, queer and non-binary people, veterans, parents, and individuals with disabilities to apply. If you need reasonable adjustments at any point in the application or interview process, please let us know and feel free to note which pronouns you use. Contract Type : Permanent Here at Havas across the group we pride ourselves on being committed to offering equal opportunities to all potential employees and have zero tolerance for discrimination. We are an equal opportunity employer and welcome applicants irrespective of age, sex, race, ethnicity, disability and other factors that have no bearing on an individual's ability to perform their job.
Jul 03, 2025
Full time
Agency : Havas Media Group Job Description : The Business Consultant is responsible for the day-to-day relationships management of a client portfolio and for the delivery of the (Mx) Media Experience services by facilitating the connection between Business client teams and Intelligence / Media Development / Measurement teams. The Havas Media Network Growth Team have been the driving force behind high profile pitch wins including Ocado, Abercrombie & Kent, ULaw and Red Bull, and several industry awards nominations and wins. We're a fast-paced, nurturing team looking for an ambitious new business and marketing manager to support the agency's growth function. The Role We are looking for an experienced New Business and Marketing Manager to join the Havas Media Growth team. This is a mid-level role, expected to create strong working relationships with employees across all levels, especially senior stakeholders. The new business and marketing manager should be highly organised and process-driven, with a clear desire to learn and progress. This person will be required to manage multiple workstreams and projects at one time, whilst continually maintaining a high work standard. They will be an excellent communicator, who values honesty, transparency and is able to ask for help. Necessary skills include the ability to display a positive attitude whilst under pressure, and successfully manage upwards to ensure workload to completed on time. They will have a keen desire, willingness and curiosity to learn about agency marketing, overall running of the business, the clients we work with, the capabilities we deliver and the wider industry. Staying abreast of new innovations, and competitors within the industry, to be able to contribute effectively to successful growth and running of the agencies. This is a great opportunity for someone with 2-5 years' experience in creative or media agencies, working in similar new business and marketing roles. Responsibilities The role has three primary areas of focus: Managing key New Biz opportunities through the full end-to-end process Delivering impactful, consistent marketing Collaborating with the wider growth function to deliver Havas Media's growth plan and ambition New Business Reviewing and sharing inbound opportunities with the New Business leadership team - New Business Director & Chief Growth Officer Support across all new business requirements such as pitch management, pitch theatre, RFI's, RFP's and creds decks Manage team communication / diarising / own research and prep / client profiles & background info Support New Business Director on all new business opportunities, including pitch management, pitch theatre, RFIs, Chemistry and Tissue meetings Tracking relevant new business external tender sites Ensure team processes and communications are run smoothly Organise and manage case study library and creation of assets Management of New Business & Marketing Team assets Marketing Own creation of marketing materials, inc management of content calendar, social, email campaigns - draft copy, plan ahead, evaluate (monthly report) Management of agency social channels, website and intermediary profiles Collaborating with the comms team to amplify our trade content Collaborate with the wider team on event management, including comms, logistics and evaluation Collaborating with strategy team on annual awards planning and entries Case study library and asset management Reporting/coordination Management and tracking of the new business pipeline and CRM reporting (agency, network and village level) Compiling competitor and industry reviews Completing ad hoc requests from the wider Havas Media Network We are looking for: Adaptability and the ability to juggle changing priorities Meticulously organised and with a keen eye for detail Natural collaborator A 'growth mindset' - hand-raising, listens to and incorporates feedback, keen to learn An individual who brings passion and energy to the team and is always looking for ways to improve what we do Someone who is accountable, reliable and honest Ability to work to tight deadlines and under pressure Demonstrable experience at senior executive/manager level in a new business, client or investment role Confidence to be able to deal with the most senior level stakeholders Strong writing skills are important Strong PowerPoint, Microsoft Outlook, Microsoft Teams, email marketing skills Havas Media Boilerplate We believe brands mean more by bringing them closer to people - and that's why our ambition is to be the most customer-centric media agency in the UK. With origins in 1987, we have decades of experience in giving a competitive edge to the likes of Domino's, British Red Cross, Homebase, Starbucks, BBC, KIA, Hyundai, Dreams and EDF, building people-first media experiences from deep audience insights and curated data threads - all backed by the scale and data power of Havas Media Network UK. Havas is an equal opportunities employer and welcomes everyone to our team. We strongly encourage people of colour, lesbian, gay, bisexual, transgender, queer and non-binary people, veterans, parents, and individuals with disabilities to apply. If you need reasonable adjustments at any point in the application or interview process, please let us know and feel free to note which pronouns you use. Contract Type : Permanent Here at Havas across the group we pride ourselves on being committed to offering equal opportunities to all potential employees and have zero tolerance for discrimination. We are an equal opportunity employer and welcome applicants irrespective of age, sex, race, ethnicity, disability and other factors that have no bearing on an individual's ability to perform their job.
Rolls Royce
Process Chemist - Submarines
Rolls Royce City, Derby
Job Description Process Chemist Full Time / Hybrid Derby, Raynesway We are looking for capable, experienced and proactive Process Chemists to join our growing team and be responsible for leading engineering packages. These are high-impact roles, ideal for experienced chemists who thrive on technical complexity, process rigour and innovation with purpose. This is an opportunity to use your deep experience in Process Chemistry to play a part in the Regeneration of the Raynesway Nuclear Licenced Site. This once in a lifetime major infrastructure programme is replacing the current facilities with modern state of the art manufacturing capability. What you will be doing You will be part of a team responsible for developing the solutions for chemistry problems and the science underpinning the design for a Nuclear Fuel Processing Plant. Providing technical advice to the Nuclear and Chemical Process engineering functions for the design and substantiation of the plant. The role will support the definition of operational limits, equipment specifications, analysis techniques and product quality requirements. The role involves the identification and evaluation of new technologies, primarily focusing on developing safe and effective chemical processes in order to meet the required product specifications and plant throughput. Defining the safe operating envelope and normal operating range for the Chemical Plant, eliminating hazards and incorporating inherent safety through process chemistry design.Defining safe and effective process chemistries in order to meet the required product specifications and plant throughput.Defining the process chemistry for the design and specification of nuclear fuel reprocessing systems, such as: liquid-liquid separation plant, material transformation processes, dissolution processes and radioactive waste treatment plants. Analysis and optioneering of alternative nuclear chemical processing technology.Facilitating laboratory trials to provide quantitative data of underpinning science support Safety Case substantiation, hazard analysis and fault analysis.Defining the analysis requirements, techniques, sampling plans and control charts for plant production and quality.Involvement in all design stages from identification of stakeholder requirements, generating and assessing options, Concept, Scheme, Front End, and Detailed Design, design substantiation and verification and validation, and installation, commissioning and operating documents.Chemical expertise input into reviews including design, quality, safety and environmental assessments and critical review, checking, verification and approval of in-house and third-party designs. Who we're looking for: At Rolls-Royce we put safety first, do the right thing, keep it simple and make a difference. These principles form the behaviours that guide us and are an essential component of our assessment process. They are the fundamental qualities that we seek for all roles. Degree in Chemistry or a related discipline.Post-graduate qualifications (Ph. D preferable)Experience in separation, waste treatment and nuclear fuel processing desirable but not essential.Membership of an appropriate Professional Engineering Institution would be preferable Why Rolls-Royce? Rolls-Royce is one of the most enduring and iconic brands in the world and has been at the forefront of innovation for over a century. We design, build and service systems that provide critical power to customers where safety and reliability are paramount. We are proud to be a force for progress, powering, protecting and connecting people everywhere. We want to ensure that the excellence and ingenuity that has shaped our history continues into our future and we need people like you to come and join us on this journey. We'll provide an environment of caring and belonging where you can be yourself. An inclusive, innovative culture that invests in you, gives you access to an incredible breadth and depth of opportunities where you can grow your career and make a difference. What we offer We offer excellent development opportunities, a competitive salary, and exceptional benefits. These include bonus, employee support assistance and employee discounts. Your needs are as unique as you are. Hybrid working is a way in which our people can balance their time between the office, home, or another remote location. It's a locally managed and flexed informal discretionary arrangement. As a minimum we're all expected to attend the workplace for collaboration and other specific reasons, on average three days per week. We are an equal opportunities employer. We're committed to developing a diverse workforce and an inclusive working environment. We believe that people from different backgrounds and cultures give us different perspectives which are crucial to innovation and problem solving. We believe the more diverse perspectives we have, the more successful we'll be. By building a culture of caring and belonging, we give everyone who works here the opportunity to realise their full potential. You can learn more about our global Inclusion strategy at Our people Rolls-Royce To work for the Rolls-Royce Submarines business an individual has to hold a Security Check clearance. Rolls-Royce will support the application for Security Clearance if you do not currently already have this in place. Due to the nature of work the business conducts and the protection of certain assets we can only progress applications from individuals who are a UK national or, in MoD approved cases, a dual national. Job Category Transformation & Operations Posting Date 25 Jun 2025; 00:06 Posting End Date 27 Jul 2025PandoLogic.
Jul 03, 2025
Full time
Job Description Process Chemist Full Time / Hybrid Derby, Raynesway We are looking for capable, experienced and proactive Process Chemists to join our growing team and be responsible for leading engineering packages. These are high-impact roles, ideal for experienced chemists who thrive on technical complexity, process rigour and innovation with purpose. This is an opportunity to use your deep experience in Process Chemistry to play a part in the Regeneration of the Raynesway Nuclear Licenced Site. This once in a lifetime major infrastructure programme is replacing the current facilities with modern state of the art manufacturing capability. What you will be doing You will be part of a team responsible for developing the solutions for chemistry problems and the science underpinning the design for a Nuclear Fuel Processing Plant. Providing technical advice to the Nuclear and Chemical Process engineering functions for the design and substantiation of the plant. The role will support the definition of operational limits, equipment specifications, analysis techniques and product quality requirements. The role involves the identification and evaluation of new technologies, primarily focusing on developing safe and effective chemical processes in order to meet the required product specifications and plant throughput. Defining the safe operating envelope and normal operating range for the Chemical Plant, eliminating hazards and incorporating inherent safety through process chemistry design.Defining safe and effective process chemistries in order to meet the required product specifications and plant throughput.Defining the process chemistry for the design and specification of nuclear fuel reprocessing systems, such as: liquid-liquid separation plant, material transformation processes, dissolution processes and radioactive waste treatment plants. Analysis and optioneering of alternative nuclear chemical processing technology.Facilitating laboratory trials to provide quantitative data of underpinning science support Safety Case substantiation, hazard analysis and fault analysis.Defining the analysis requirements, techniques, sampling plans and control charts for plant production and quality.Involvement in all design stages from identification of stakeholder requirements, generating and assessing options, Concept, Scheme, Front End, and Detailed Design, design substantiation and verification and validation, and installation, commissioning and operating documents.Chemical expertise input into reviews including design, quality, safety and environmental assessments and critical review, checking, verification and approval of in-house and third-party designs. Who we're looking for: At Rolls-Royce we put safety first, do the right thing, keep it simple and make a difference. These principles form the behaviours that guide us and are an essential component of our assessment process. They are the fundamental qualities that we seek for all roles. Degree in Chemistry or a related discipline.Post-graduate qualifications (Ph. D preferable)Experience in separation, waste treatment and nuclear fuel processing desirable but not essential.Membership of an appropriate Professional Engineering Institution would be preferable Why Rolls-Royce? Rolls-Royce is one of the most enduring and iconic brands in the world and has been at the forefront of innovation for over a century. We design, build and service systems that provide critical power to customers where safety and reliability are paramount. We are proud to be a force for progress, powering, protecting and connecting people everywhere. We want to ensure that the excellence and ingenuity that has shaped our history continues into our future and we need people like you to come and join us on this journey. We'll provide an environment of caring and belonging where you can be yourself. An inclusive, innovative culture that invests in you, gives you access to an incredible breadth and depth of opportunities where you can grow your career and make a difference. What we offer We offer excellent development opportunities, a competitive salary, and exceptional benefits. These include bonus, employee support assistance and employee discounts. Your needs are as unique as you are. Hybrid working is a way in which our people can balance their time between the office, home, or another remote location. It's a locally managed and flexed informal discretionary arrangement. As a minimum we're all expected to attend the workplace for collaboration and other specific reasons, on average three days per week. We are an equal opportunities employer. We're committed to developing a diverse workforce and an inclusive working environment. We believe that people from different backgrounds and cultures give us different perspectives which are crucial to innovation and problem solving. We believe the more diverse perspectives we have, the more successful we'll be. By building a culture of caring and belonging, we give everyone who works here the opportunity to realise their full potential. You can learn more about our global Inclusion strategy at Our people Rolls-Royce To work for the Rolls-Royce Submarines business an individual has to hold a Security Check clearance. Rolls-Royce will support the application for Security Clearance if you do not currently already have this in place. Due to the nature of work the business conducts and the protection of certain assets we can only progress applications from individuals who are a UK national or, in MoD approved cases, a dual national. Job Category Transformation & Operations Posting Date 25 Jun 2025; 00:06 Posting End Date 27 Jul 2025PandoLogic.
Matchtech
Laboratory Technician
Matchtech Fawley, Hampshire
This is an opportunity for a Laboratory Technician to support routine and incident based environmental testing within an oil refining and petrochemical environment. The successful Laboratory Technician will conduct daily environmental analyses / laboratory analyses on plant effluent streams, perform laboratory testing in response to company incidents, and contribute to overall environmental monitoring efforts. This position is ideal for a candidate with a strong chemistry background and a passion for environmental quality assurance. Key Responsibilities: Perform routine and ad-hoc laboratory analyses (wet chemistry) on plant product and process samples to support quality assurance and compliance. Conduct tests including, but not limited to, metals analysis using Atomic Absorption (AA), Microbial Growth (MBG), Gas Chromatography (GC), Fourier Transform Infrared Spectroscopy (FTIR) and various titrations. Prepare chemical stock solutions, reagents, and calibration standards according to standard procedures. Ensure accurate and timely data recording and reporting using the Laboratory Information Management System (LIMS). Maintain lab cleanliness and safety in accordance with established protocols. Support the resolution of quality control issues using appropriate analytical methods and equipment. Qualifications and Skills: Bachelor's degree (or equivalent) in Chemistry, Environmental Science, Engineering, or a related STEM discipline. Alternatively, relevant and demonstrable laboratory work experience will be considered. Proficiency with computers; experience using quality control or LIMS systems is preferred. Strong attention to detail with the ability to work independently and manage priorities effectively. Experience in environmental water analysis is highly desirable. Knowledge of and hands-on experience with analytical instruments such as GC, FTIR, and AA, including calibration and maintenance, is a strong asset. This role is Inside IR35. The rates advertised are PAYE.
Jul 03, 2025
Contractor
This is an opportunity for a Laboratory Technician to support routine and incident based environmental testing within an oil refining and petrochemical environment. The successful Laboratory Technician will conduct daily environmental analyses / laboratory analyses on plant effluent streams, perform laboratory testing in response to company incidents, and contribute to overall environmental monitoring efforts. This position is ideal for a candidate with a strong chemistry background and a passion for environmental quality assurance. Key Responsibilities: Perform routine and ad-hoc laboratory analyses (wet chemistry) on plant product and process samples to support quality assurance and compliance. Conduct tests including, but not limited to, metals analysis using Atomic Absorption (AA), Microbial Growth (MBG), Gas Chromatography (GC), Fourier Transform Infrared Spectroscopy (FTIR) and various titrations. Prepare chemical stock solutions, reagents, and calibration standards according to standard procedures. Ensure accurate and timely data recording and reporting using the Laboratory Information Management System (LIMS). Maintain lab cleanliness and safety in accordance with established protocols. Support the resolution of quality control issues using appropriate analytical methods and equipment. Qualifications and Skills: Bachelor's degree (or equivalent) in Chemistry, Environmental Science, Engineering, or a related STEM discipline. Alternatively, relevant and demonstrable laboratory work experience will be considered. Proficiency with computers; experience using quality control or LIMS systems is preferred. Strong attention to detail with the ability to work independently and manage priorities effectively. Experience in environmental water analysis is highly desirable. Knowledge of and hands-on experience with analytical instruments such as GC, FTIR, and AA, including calibration and maintenance, is a strong asset. This role is Inside IR35. The rates advertised are PAYE.
Senior Compiler Engineer
Riverlane Cambridge, Cambridgeshire
Cambridge, UK Full-time Permanent Hybrid Salary: £65,000 - £80,000 GBP DOE We will also consider part-time applications for this role. Please indicate your preferred working schedule in your cover letter. We are able to consider a range of levels of experience for this position, and are therefore advertising this role at different levels of seniority. Please only apply to the role that you feel best suits your skills and experience. About us Riverlane's mission is to make quantum computing useful, sooner. From advances in material science to complex chemistry simulation for drug design and discovery, quantum computers will help solve some of the world's most important challenges. Riverlane is building the quantum error correction stack, Deltaflow, to make this happen. It's a complex problem that requires a range of skills, talent and passion. We recently raised $75M in Series C funding to accelerate our cutting-edge R&D in quantum error correction (QEC), and are partnering with many of the world's leading quantum hardware providers and government agencies to make fault-tolerant quantum computing a reality. We're making remarkable progress and growing fast. About the role Our Tooling team are building out the compilation toolchain for fault tolerant quantum computing. The compiler enables the quantum computer user to use representations of novel error correcting codes, and to execute their programs with new real-time decoders. This role is a fantastic opportunity to help us do this. You don't need a background in quantum computing to be successful in this role - quantum engineering requires a wide range of skills and disciplines, including classical computing skills. By applying your existing knowledge of computer science fundamentals, you will help Riverlane to build the critical compilation and runtime systems needed for this unique computing system. You will learn quantum computing along the way! Riverlane's mission is exciting, but complex. It requires teams with a wide range of skills and perspectives, that communicate well and collaborate effectively to achieve truly innovative solutions. You will thrive in an environment where knowledge-sharing and continuous learning are the norm. We are moving fast in a brand-new market, where requirements change as the technology evolves, so the ability to adapt is important. What you will do Design and build system tools such as compilers, schedulers and debuggers Develop functional and performance models of control systems and Deltaflow hardware (our quantum error correction stack) Write correct, maintainable and fast code Enable users to write and run fault tolerant programs Build the software stack for error-corrected quantum computing systems Work with scientists and engineers to implement new error correcting codes, and runtimes for new decoders What we need Experience of shipping real software to real users Curiosity to learn new things Experience of working collaboratively, with a diverse range of people Broad knowledge of the whole software and hardware stack: compilers, operating systems, computer architectures Deep experience with LLVM MLIR, GCC, or other compiler toolchains Expertise in Python; expertise in C++ or Rust Interest in working in the quantum open-source ecosystem Excellent communication skills, both written and verbal What you can expect from us A comprehensive benefits package, including annual bonus scheme, private medical insurance, life insurance, a contributory pension scheme (and much more) Equity so that our team can share in the long-term success of Riverlane 28 days annual leave (plus bank holidays) and enhanced family leave A diverse work environment that brings together experts in many fields (including software and hardware development, quantum information theory, physics, maths and many more) and over 20 different nationalities A learning environment that encourages individual, team and company growth and learning, including an annual training and conference budget How to apply Please upload a CV and cover letter by clicking 'Apply'. Your cover letter should explain why you are applying for the job and what skills and experience you can bring to the role. We review CVs as we receive them and interview as soon as we have applications that look like a good match. We do not use closing dates. So, please apply as soon as possible to avoid missing out on this role. If you have any queries, please contact . Everyone is welcome at Riverlane. We are an equal opportunities employer and encourage applications from eligible and suitably qualified candidates regardless of age, disability, ethnicity, gender, gender reassignment, religion or belief, sexual orientation, marital or civil partnership status, or pregnancy and maternity/paternity. Studies have shown that women tend to apply to jobs if they meet all or almost all of the requirements whereas men apply even if they meet only some of the requirements. If that sounds like you then please apply - we are happy to review your application and let you know if we think you might be a good fit. If you need any adjustments made to the application or selection process so you can do your best, please let us know. We will be happy to help.
Jul 02, 2025
Full time
Cambridge, UK Full-time Permanent Hybrid Salary: £65,000 - £80,000 GBP DOE We will also consider part-time applications for this role. Please indicate your preferred working schedule in your cover letter. We are able to consider a range of levels of experience for this position, and are therefore advertising this role at different levels of seniority. Please only apply to the role that you feel best suits your skills and experience. About us Riverlane's mission is to make quantum computing useful, sooner. From advances in material science to complex chemistry simulation for drug design and discovery, quantum computers will help solve some of the world's most important challenges. Riverlane is building the quantum error correction stack, Deltaflow, to make this happen. It's a complex problem that requires a range of skills, talent and passion. We recently raised $75M in Series C funding to accelerate our cutting-edge R&D in quantum error correction (QEC), and are partnering with many of the world's leading quantum hardware providers and government agencies to make fault-tolerant quantum computing a reality. We're making remarkable progress and growing fast. About the role Our Tooling team are building out the compilation toolchain for fault tolerant quantum computing. The compiler enables the quantum computer user to use representations of novel error correcting codes, and to execute their programs with new real-time decoders. This role is a fantastic opportunity to help us do this. You don't need a background in quantum computing to be successful in this role - quantum engineering requires a wide range of skills and disciplines, including classical computing skills. By applying your existing knowledge of computer science fundamentals, you will help Riverlane to build the critical compilation and runtime systems needed for this unique computing system. You will learn quantum computing along the way! Riverlane's mission is exciting, but complex. It requires teams with a wide range of skills and perspectives, that communicate well and collaborate effectively to achieve truly innovative solutions. You will thrive in an environment where knowledge-sharing and continuous learning are the norm. We are moving fast in a brand-new market, where requirements change as the technology evolves, so the ability to adapt is important. What you will do Design and build system tools such as compilers, schedulers and debuggers Develop functional and performance models of control systems and Deltaflow hardware (our quantum error correction stack) Write correct, maintainable and fast code Enable users to write and run fault tolerant programs Build the software stack for error-corrected quantum computing systems Work with scientists and engineers to implement new error correcting codes, and runtimes for new decoders What we need Experience of shipping real software to real users Curiosity to learn new things Experience of working collaboratively, with a diverse range of people Broad knowledge of the whole software and hardware stack: compilers, operating systems, computer architectures Deep experience with LLVM MLIR, GCC, or other compiler toolchains Expertise in Python; expertise in C++ or Rust Interest in working in the quantum open-source ecosystem Excellent communication skills, both written and verbal What you can expect from us A comprehensive benefits package, including annual bonus scheme, private medical insurance, life insurance, a contributory pension scheme (and much more) Equity so that our team can share in the long-term success of Riverlane 28 days annual leave (plus bank holidays) and enhanced family leave A diverse work environment that brings together experts in many fields (including software and hardware development, quantum information theory, physics, maths and many more) and over 20 different nationalities A learning environment that encourages individual, team and company growth and learning, including an annual training and conference budget How to apply Please upload a CV and cover letter by clicking 'Apply'. Your cover letter should explain why you are applying for the job and what skills and experience you can bring to the role. We review CVs as we receive them and interview as soon as we have applications that look like a good match. We do not use closing dates. So, please apply as soon as possible to avoid missing out on this role. If you have any queries, please contact . Everyone is welcome at Riverlane. We are an equal opportunities employer and encourage applications from eligible and suitably qualified candidates regardless of age, disability, ethnicity, gender, gender reassignment, religion or belief, sexual orientation, marital or civil partnership status, or pregnancy and maternity/paternity. Studies have shown that women tend to apply to jobs if they meet all or almost all of the requirements whereas men apply even if they meet only some of the requirements. If that sounds like you then please apply - we are happy to review your application and let you know if we think you might be a good fit. If you need any adjustments made to the application or selection process so you can do your best, please let us know. We will be happy to help.
Kerry
RD&A Technologist - Taste Fermentation
Kerry Menstrie, Clackmannanshire
About Kerry Kerry is the world's leading taste and nutrition company for the food, beverage and pharmaceutical industries. Every day we partner with customers to create healthier, tastier and more sustainable products that are consumed by billions of people across the world. Our vision is to be our customers' most valued partner, creating a world of sustainable nutrition. A career with Kerry offers you an opportunity to shape the future of food while providing you opportunities to explore and grow in a truly global environment. About the role We are recruiting for an RD&A Technologist to work alongside the Taste Fermentation RD&A team in Menstrie, Scotland. You will support on R&D projects aiming to develop new products and improve current production processes. The activities involved in these tasks cover, but are not limited to, the performance of bench-scale reactions and fermentations, the testing of newly developed concepts using analytical instruments, and the implementation of new methods and processes. Key responsibilities Process and report experimental results, playing a key role in reporting to project stakeholders. Actively participate in project meetings and reviews, providing critical feedback and technology insights. Share the responsibility of maintaining the smooth operation of the lab, in terms of maintenance, hygiene, consumables, procedures and QSHE (Quality, Safety, Health and Environment), as well as participating in the selection/commissioning of new equipment. Work with Kerry systems supporting the administrative work encompassing RD&A. Contribute innovative ideation towards new product development and improvement in existing production processes. Robust execution of experiments that will confidently drive advancement of technical knowledge and support decision-making processes. Technical reporting of experiments, supporting timely R&D project delivery and documentation for technology transfers. Full support of administrative tasks related to RD&A activities. Laboratory management and maintenance, ensuring facilities and equipment are fit-for-purpose and operating smoothly. Qualifications and skills BSc. in Microbiology, Biotechnology, Chemistry or related field. Experience in microbial fermentation, either in industrial or academic settings. Experience with biological and analytical techniques (biochemical assays, HPLC, etc). Competence in general microbiology laboratory practices and aseptic techniques. Competence in writing technical documents such as research reports, SOPs, etc. Proficiency with Excel or other data processing software is highly desirable. Experience with pilot-scale facilities or in production environment is a plus. Experience in scaling-up and transferring new technologies to manufacturing is a plus. Capable of working in collaborative and multi-cultural environments.
Jul 02, 2025
Full time
About Kerry Kerry is the world's leading taste and nutrition company for the food, beverage and pharmaceutical industries. Every day we partner with customers to create healthier, tastier and more sustainable products that are consumed by billions of people across the world. Our vision is to be our customers' most valued partner, creating a world of sustainable nutrition. A career with Kerry offers you an opportunity to shape the future of food while providing you opportunities to explore and grow in a truly global environment. About the role We are recruiting for an RD&A Technologist to work alongside the Taste Fermentation RD&A team in Menstrie, Scotland. You will support on R&D projects aiming to develop new products and improve current production processes. The activities involved in these tasks cover, but are not limited to, the performance of bench-scale reactions and fermentations, the testing of newly developed concepts using analytical instruments, and the implementation of new methods and processes. Key responsibilities Process and report experimental results, playing a key role in reporting to project stakeholders. Actively participate in project meetings and reviews, providing critical feedback and technology insights. Share the responsibility of maintaining the smooth operation of the lab, in terms of maintenance, hygiene, consumables, procedures and QSHE (Quality, Safety, Health and Environment), as well as participating in the selection/commissioning of new equipment. Work with Kerry systems supporting the administrative work encompassing RD&A. Contribute innovative ideation towards new product development and improvement in existing production processes. Robust execution of experiments that will confidently drive advancement of technical knowledge and support decision-making processes. Technical reporting of experiments, supporting timely R&D project delivery and documentation for technology transfers. Full support of administrative tasks related to RD&A activities. Laboratory management and maintenance, ensuring facilities and equipment are fit-for-purpose and operating smoothly. Qualifications and skills BSc. in Microbiology, Biotechnology, Chemistry or related field. Experience in microbial fermentation, either in industrial or academic settings. Experience with biological and analytical techniques (biochemical assays, HPLC, etc). Competence in general microbiology laboratory practices and aseptic techniques. Competence in writing technical documents such as research reports, SOPs, etc. Proficiency with Excel or other data processing software is highly desirable. Experience with pilot-scale facilities or in production environment is a plus. Experience in scaling-up and transferring new technologies to manufacturing is a plus. Capable of working in collaborative and multi-cultural environments.
CK GROUP
Environmental Scientist
CK GROUP Barnsley, Yorkshire
CK Group are recruiting for a Environmental Scientist, to join our client who are Consultants in Damage Assessment & Business Recovery, in the damage management industry, at their site in Sheffield. This is a permanent role with a salary of £30,000 to £40,000 per annum, depending on experience. This role will include travel, so you must hold a full driving licence and have access to a car. The Company: Our clients are independent consultants in damage assessment and business recovery. This company provides their clients with scientifically and technically supported advice on complex losses in both commercial and residential property. They are a well-established family run business, known and respected throughout the damage management industry. Location: This role is located in Sheffield with travel to other sites as and when required. The Role: Analysing test samples, including: Gravimetric moisture testing, Ion chromatography, FT-Infrared spectroscopy, Scanning electron microscopy, DNA sequencing of biological samples. Collation of analysis of data. Preparing technical reports. Carrying out site inspections and a variety of on-site environmental test sampling. Undertaking technical surveying methods such as 360 photogrammetry and drone surveys. Your Background: Academic background in a chemistry or environmental science related discipline. 3+ years of experience of collecting, analysing, interpreting and reporting on environmental samples. Organised and diligent, with the ability to record and report information quickly and accurately. Process driven, and able to adhere to stringent scientific methodology and processes. Analytically minded, with experience of field and/or laboratory testing methodologies. Independently minded, with a willingness to balance laboratory work with customer s needs in attending properties to undertake sampling. Apply: It is essential that applicants hold entitlement to work in the UK. Please quote job reference in all correspondence. If this position isn't suitable but you are looking for a new role, or if you are interested in seeing what opportunities are out there, head over to our LinkedIn page (cka-group) and follow us to see our latest jobs and company news. INDCH
Jul 02, 2025
Full time
CK Group are recruiting for a Environmental Scientist, to join our client who are Consultants in Damage Assessment & Business Recovery, in the damage management industry, at their site in Sheffield. This is a permanent role with a salary of £30,000 to £40,000 per annum, depending on experience. This role will include travel, so you must hold a full driving licence and have access to a car. The Company: Our clients are independent consultants in damage assessment and business recovery. This company provides their clients with scientifically and technically supported advice on complex losses in both commercial and residential property. They are a well-established family run business, known and respected throughout the damage management industry. Location: This role is located in Sheffield with travel to other sites as and when required. The Role: Analysing test samples, including: Gravimetric moisture testing, Ion chromatography, FT-Infrared spectroscopy, Scanning electron microscopy, DNA sequencing of biological samples. Collation of analysis of data. Preparing technical reports. Carrying out site inspections and a variety of on-site environmental test sampling. Undertaking technical surveying methods such as 360 photogrammetry and drone surveys. Your Background: Academic background in a chemistry or environmental science related discipline. 3+ years of experience of collecting, analysing, interpreting and reporting on environmental samples. Organised and diligent, with the ability to record and report information quickly and accurately. Process driven, and able to adhere to stringent scientific methodology and processes. Analytically minded, with experience of field and/or laboratory testing methodologies. Independently minded, with a willingness to balance laboratory work with customer s needs in attending properties to undertake sampling. Apply: It is essential that applicants hold entitlement to work in the UK. Please quote job reference in all correspondence. If this position isn't suitable but you are looking for a new role, or if you are interested in seeing what opportunities are out there, head over to our LinkedIn page (cka-group) and follow us to see our latest jobs and company news. INDCH
Kerry
Quality Specialist
Kerry Coleraine, County Londonderry
Requisition ID: 58612 Position Type: FT Permanent Workplace Arrangement: About the role We have a great opportunity for a Quality Specialist to join us, at our site in Coleraine. This is an exciting role, working within the quality team and alongside the wider supply chain, production and lab teams on site to ensure food safety, quality and regulatory compliance. It would suit someone with previous quality experience, looking for an opportunity to develop their career further. Hours of Work - Typically, Monday - Friday. There is a requirement for flexibility to cover weekend hours as required and project specific requirements. About Kerry Dairy Ireland Kerry Dairy Ireland is a vertically integrated farm-to-fork business with a very substantial consumer foods presence and a leading nutritional and dairy ingredients division, delivering high-quality dairy solutions with a focus on sustainability and innovation. From partnering with local family farms to producing world-class dairy products, we ensure every step of our value chain reflects our commitment to excellence. With over 50 years' experience in milk processing, dairy and nutritional technology advancement, and product innovation, we are a key stakeholder in the global food industry and creators of a strong portfolio of market leading dairy brands including Cheestrings, Charleville and Coleraine Cheese, Dairygold, Golden Cow and our new SMUG range. Our from food, for food culture and deep-rooted connection to our 2,800 milk suppliers differentiates our business and offers captivating opportunities for our customers and consumers. Our dairy comes from some of the world's richest grazing land and is produced by a network of Irish family farms that have one of the lowest carbon footprints in the world. Through a combination of expertise, innovation, and sustainability, Kerry Dairy Ireland is proud to shape the future of dairy while meeting the diverse needs of our farmers, customers, and communities. Headquartered in Tralee, Co. Kerry, we operate multiple manufacturing facilities in the southwest of Ireland, including Listowel, Charleville, Newmarket, and Farranfore. Additionally, we manage 29 Farm & Home stores throughout the region, ensuring comprehensive coverage and service. In Northern Ireland and the United Kingdom, our presence extends to key locations in Portadown, Coleraine, and Ossett. Globally, Kerry Dairy Ireland employs over 1,600 dedicated professionals across Ireland, Northern Ireland, the UK, USA, Netherlands, Spain, Germany, and China. In 2024, we achieved a turnover of approximately €1.3 billion, reflecting our commitment to excellence and growth. What you'll be doing You will be responsible for the process verification and control of non-conformity overarching processes. This includes but is not limited to: Conducting food safety risk assessments Delivery of high standards of plant hygiene which will include, training, hygiene verification & validation Manage food safety aspects of projects such as equipment modification/relocation and optimizing operational efficiencies. Set the standards for testing methods Confirm results on internal systems to ensure customer compliance Process and equipment verification. The role also involves the following overarching QSHE processes: FSQ Processes, HACCP, Standards, Templates Regional FSQ KPI Setting & Execution Employee Engagement Process Equipment inspections Risk Management/Compliance Assurance Quality Internal audits Monthly Hygiene Audits Training to include - sampling techniques/best practice, swabbing techniques & ATP Technical support to include - Positive release and support and cover for colleagues within the department What you can bring to the role A relevant qualification in Science, Food Science, Biochemistry or equivalent HACCP Training Food manufacturing experience Attention to detail coupled with strong problem solving ability Team focus -strong Interpersonal skills Excellent verbal and written communication skills Proficient in the use of MS Office tools A demonstrated numerical ability to record, interpret and analyse key process data Ability to adapt to a fast paced environment with changing requirements Internal auditing experience would be beneficial Experience of working with retailers would be beneficial Kerry is an Equal Opportunities Employer. Consistent with our policy of providing equality of opportunity for all, we are required to seek particular information from applicants. As part of your application you will be asked to answer a short number of questions. This information will be held separate to your application and treated in the strictest of confidence. Beware of scams online or from individuals claiming to represent us. A Kerry employee will not solicit candidates through a non-Kerry email address or phone number. In addition, Kerry does not currently utilise video chat rooms (e.g., Google Hangouts) to conduct interviews. Refuse any request that asks you to provide payment to participate in the hiring process (e.g., purchasing a "starter kit," investing in training, or something similar). Kerry will not ask you to pay any money at any point in the hiring process with the exception of reimbursable travel expenses. In addition, any payments made by Kerry will be from official firm accounts bearing the Kerry name. Recruiter: Posting Type: LI Please note: We do not accept CVs or candidate profiles from recruitment agencies where Kerry terms of business have not been signed. Additionally, we will not consider or agree to payment of any recruiter fee under these circumstances. This also applies to CVs or candidate profiles sent directly to any Kerry Hiring Managers .
Jul 02, 2025
Full time
Requisition ID: 58612 Position Type: FT Permanent Workplace Arrangement: About the role We have a great opportunity for a Quality Specialist to join us, at our site in Coleraine. This is an exciting role, working within the quality team and alongside the wider supply chain, production and lab teams on site to ensure food safety, quality and regulatory compliance. It would suit someone with previous quality experience, looking for an opportunity to develop their career further. Hours of Work - Typically, Monday - Friday. There is a requirement for flexibility to cover weekend hours as required and project specific requirements. About Kerry Dairy Ireland Kerry Dairy Ireland is a vertically integrated farm-to-fork business with a very substantial consumer foods presence and a leading nutritional and dairy ingredients division, delivering high-quality dairy solutions with a focus on sustainability and innovation. From partnering with local family farms to producing world-class dairy products, we ensure every step of our value chain reflects our commitment to excellence. With over 50 years' experience in milk processing, dairy and nutritional technology advancement, and product innovation, we are a key stakeholder in the global food industry and creators of a strong portfolio of market leading dairy brands including Cheestrings, Charleville and Coleraine Cheese, Dairygold, Golden Cow and our new SMUG range. Our from food, for food culture and deep-rooted connection to our 2,800 milk suppliers differentiates our business and offers captivating opportunities for our customers and consumers. Our dairy comes from some of the world's richest grazing land and is produced by a network of Irish family farms that have one of the lowest carbon footprints in the world. Through a combination of expertise, innovation, and sustainability, Kerry Dairy Ireland is proud to shape the future of dairy while meeting the diverse needs of our farmers, customers, and communities. Headquartered in Tralee, Co. Kerry, we operate multiple manufacturing facilities in the southwest of Ireland, including Listowel, Charleville, Newmarket, and Farranfore. Additionally, we manage 29 Farm & Home stores throughout the region, ensuring comprehensive coverage and service. In Northern Ireland and the United Kingdom, our presence extends to key locations in Portadown, Coleraine, and Ossett. Globally, Kerry Dairy Ireland employs over 1,600 dedicated professionals across Ireland, Northern Ireland, the UK, USA, Netherlands, Spain, Germany, and China. In 2024, we achieved a turnover of approximately €1.3 billion, reflecting our commitment to excellence and growth. What you'll be doing You will be responsible for the process verification and control of non-conformity overarching processes. This includes but is not limited to: Conducting food safety risk assessments Delivery of high standards of plant hygiene which will include, training, hygiene verification & validation Manage food safety aspects of projects such as equipment modification/relocation and optimizing operational efficiencies. Set the standards for testing methods Confirm results on internal systems to ensure customer compliance Process and equipment verification. The role also involves the following overarching QSHE processes: FSQ Processes, HACCP, Standards, Templates Regional FSQ KPI Setting & Execution Employee Engagement Process Equipment inspections Risk Management/Compliance Assurance Quality Internal audits Monthly Hygiene Audits Training to include - sampling techniques/best practice, swabbing techniques & ATP Technical support to include - Positive release and support and cover for colleagues within the department What you can bring to the role A relevant qualification in Science, Food Science, Biochemistry or equivalent HACCP Training Food manufacturing experience Attention to detail coupled with strong problem solving ability Team focus -strong Interpersonal skills Excellent verbal and written communication skills Proficient in the use of MS Office tools A demonstrated numerical ability to record, interpret and analyse key process data Ability to adapt to a fast paced environment with changing requirements Internal auditing experience would be beneficial Experience of working with retailers would be beneficial Kerry is an Equal Opportunities Employer. Consistent with our policy of providing equality of opportunity for all, we are required to seek particular information from applicants. As part of your application you will be asked to answer a short number of questions. This information will be held separate to your application and treated in the strictest of confidence. Beware of scams online or from individuals claiming to represent us. A Kerry employee will not solicit candidates through a non-Kerry email address or phone number. In addition, Kerry does not currently utilise video chat rooms (e.g., Google Hangouts) to conduct interviews. Refuse any request that asks you to provide payment to participate in the hiring process (e.g., purchasing a "starter kit," investing in training, or something similar). Kerry will not ask you to pay any money at any point in the hiring process with the exception of reimbursable travel expenses. In addition, any payments made by Kerry will be from official firm accounts bearing the Kerry name. Recruiter: Posting Type: LI Please note: We do not accept CVs or candidate profiles from recruitment agencies where Kerry terms of business have not been signed. Additionally, we will not consider or agree to payment of any recruiter fee under these circumstances. This also applies to CVs or candidate profiles sent directly to any Kerry Hiring Managers .

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