ABOUT YOU This role is ideal for an experienced bioanalytical LC-MS/MS scientist who enjoys working independently, applying technical expertise to complex quantitative analysis, and collaborating closely with colleagues and clients. You will bring strong technical capability, confidence in method development and validation, and the ability to communicate clearly on both scientific and commercial click apply for full job details
Feb 15, 2026
Full time
ABOUT YOU This role is ideal for an experienced bioanalytical LC-MS/MS scientist who enjoys working independently, applying technical expertise to complex quantitative analysis, and collaborating closely with colleagues and clients. You will bring strong technical capability, confidence in method development and validation, and the ability to communicate clearly on both scientific and commercial click apply for full job details
.Our vision is to create a charity where everyone feels like they belong, benefits from and participates in, the work we do. We actively encourage applications from people of all backgrounds and cultures, in particular those from ethnic minority backgrounds who are currently under-represented.We want to see every candidate performing at their best throughout the job application process, interview process and whilst at work. We therefore ask you to inform us of any concerns you have or any adjustments you might need to enable this to happen. Please contact or 0 as soon as possible. Unfortunately, we are unable to recruit anyone below the age of 18, so that we can protect young people from health & safety and safeguarding risks. Senior Principal Scientist (Network Translation) £58,400 - £76,000 plus Department: Therapeutic Innovation - R&I Reports to: Chief Scientific Officer Location: Babraham Research Campus, Cambridge with high flex (1 to 2 days per week on site) Contract type/hours: Permanent, Full time 35 hours per week (flexible working requests will be considered) Closing date: Sunday 1st March 23:55pm Interview Date: Approximately week commencing 9th/16th March Interview process: Competency based interview with task/presentation At Cancer Research UK, we exist to beat cancer. At Cancer Research Horizons (CRH) our Therapeutic Innovation team is investing in a world leading capability to translate breakthrough discovery science into the next generation of oncology therapeutics. As part of this evolution, we are establishing a new Network Translation team. A group of experienced oncology drug discoverers dedicated to identifying, shaping, and accelerating the most exciting science emerging from the CRUK research ecosystem. Every role at CRH is united by a single mission: beating cancer sooner. We carry out work that matters - impacting patients, families, and the future of scienceAs a Senior Principal Scientist, you will play a pivotal role in evaluating the breadth of CRUK's research portfolio, as well as emerging scientific areas with strong therapeutic potential. Working across CRUK Institutes, Centres, and international academic collaborations, you will build trusted relationships with scientific leaders to uncover early stage ideas with the potential to become validated, fundable therapeutic concepts.This is an outward facing, high visibility role that requires deep scientific insight, strategic judgement, and a natural curiosity for uncovering translational opportunity before it becomes obvious. You will help transform breakthrough biology into new medicines for cancer patients, shaping not only individual projects, but the future direction of CRUK funded oncology research itself.This position offers a rare opportunity for an accomplished drug hunter to influence therapeutic innovation on a national scale and support the discovery of tomorrow's cancer therapies. You'll be joining over 200 staff across CRH from both industrial and academic backgrounds, all dedicated to bringing forward the day we cure cancer. Support the implementation of a new Network Translation strategy for CRH TI to enhance the number of therapeutic opportunities identified from CRUK funded research. Maintain awareness of emerging areas of cancer biology and technological advances relevant to the objectives of CRH TI in order to identify and recommend priority translational opportunities for examination or investment. Analyse current and future CRUK funded research to highlight key translational opportunities. Work with CRUK PIs, Research Institutes and Centres, within the UK and internationally (CRUK/NCI Grand Challenges or Academic Alliances) to identify translational opportunities. Perform detailed reviews of opportunities identified. Shape new hypotheses and collaborative proposals in partnership with PIs. Signpost the Therapeutic Catalyst scheme and assist the development and submission of EOI proposals. Propose translational opportunities for strategic interventional funding. Propose opportunities for consideration as TI collaborations and for experimental validation by TI's Portfolio Generation. Promote the visibility of the Network Translation team in the academic research community and life science sector. PhD or equivalent in a relevant discipline (e.g. Bioscience, Chemical Biology) with previous experience of working on oncology drug discovery in industry. You will have expertise in identifying and developing small molecule therapies and/or biotherapeutics, with an awareness of alternative therapeutic modalities. A good understanding of mechanistic cancer biology, current therapeutic approaches in oncology, and personalised medicine strategies applied to cancer treatment. A good understanding of translating opportunities from a target concept to a therapeutic, including relevant target validation methods and the use of preclinical models. Previous experience of working productively with or within the academic sector on translational/therapeutic projects. Knowledge of the broad drug development pipeline, from Target Identification through to clinical development. Excellent interpersonal skills with the ability to network and build strong working relationships. Excellent written and verbal communication skills. Strong and collaborative team player. Self-motivated individual with excellent time-management skills, able to prioritise workload and deliver to tight deadlines.Our organisation values are designed to guide all that we do. Bold: Act with ambition, courage and determination Credible: Act with rigour and professionalism Human : Act to have a positive impact on people Together: Act inclusively and collaboratively We're looking for people who can believe in and embody these organisation values and can use them to drive forward progress against our mission to beat cancer.If you're interested in applying and excited about working with us but are unsure if you have the right skills and experience, we'd still love to hear from you.We create a working environment that supports your wellbeing and provide a generous benefits package, a wide range of career and personal development opportunities and high-quality tools. Our policies and processes enable you to improve your work-life balance and take positive steps in your career.You can explore our benefits by visiting our .We operate an anonymised shortlisting process in our commitment to equality, diversity and inclusion. CVs are required for all applications; but we won't be able to view them until we invite you for an interview. Instead, we ask you to complete the work history section of the online application form for us to be able to assess you fairly and objectively.For more information on this career opportunity please or contact us at more updates on our work and careers, follow us on: and .
Feb 15, 2026
Full time
.Our vision is to create a charity where everyone feels like they belong, benefits from and participates in, the work we do. We actively encourage applications from people of all backgrounds and cultures, in particular those from ethnic minority backgrounds who are currently under-represented.We want to see every candidate performing at their best throughout the job application process, interview process and whilst at work. We therefore ask you to inform us of any concerns you have or any adjustments you might need to enable this to happen. Please contact or 0 as soon as possible. Unfortunately, we are unable to recruit anyone below the age of 18, so that we can protect young people from health & safety and safeguarding risks. Senior Principal Scientist (Network Translation) £58,400 - £76,000 plus Department: Therapeutic Innovation - R&I Reports to: Chief Scientific Officer Location: Babraham Research Campus, Cambridge with high flex (1 to 2 days per week on site) Contract type/hours: Permanent, Full time 35 hours per week (flexible working requests will be considered) Closing date: Sunday 1st March 23:55pm Interview Date: Approximately week commencing 9th/16th March Interview process: Competency based interview with task/presentation At Cancer Research UK, we exist to beat cancer. At Cancer Research Horizons (CRH) our Therapeutic Innovation team is investing in a world leading capability to translate breakthrough discovery science into the next generation of oncology therapeutics. As part of this evolution, we are establishing a new Network Translation team. A group of experienced oncology drug discoverers dedicated to identifying, shaping, and accelerating the most exciting science emerging from the CRUK research ecosystem. Every role at CRH is united by a single mission: beating cancer sooner. We carry out work that matters - impacting patients, families, and the future of scienceAs a Senior Principal Scientist, you will play a pivotal role in evaluating the breadth of CRUK's research portfolio, as well as emerging scientific areas with strong therapeutic potential. Working across CRUK Institutes, Centres, and international academic collaborations, you will build trusted relationships with scientific leaders to uncover early stage ideas with the potential to become validated, fundable therapeutic concepts.This is an outward facing, high visibility role that requires deep scientific insight, strategic judgement, and a natural curiosity for uncovering translational opportunity before it becomes obvious. You will help transform breakthrough biology into new medicines for cancer patients, shaping not only individual projects, but the future direction of CRUK funded oncology research itself.This position offers a rare opportunity for an accomplished drug hunter to influence therapeutic innovation on a national scale and support the discovery of tomorrow's cancer therapies. You'll be joining over 200 staff across CRH from both industrial and academic backgrounds, all dedicated to bringing forward the day we cure cancer. Support the implementation of a new Network Translation strategy for CRH TI to enhance the number of therapeutic opportunities identified from CRUK funded research. Maintain awareness of emerging areas of cancer biology and technological advances relevant to the objectives of CRH TI in order to identify and recommend priority translational opportunities for examination or investment. Analyse current and future CRUK funded research to highlight key translational opportunities. Work with CRUK PIs, Research Institutes and Centres, within the UK and internationally (CRUK/NCI Grand Challenges or Academic Alliances) to identify translational opportunities. Perform detailed reviews of opportunities identified. Shape new hypotheses and collaborative proposals in partnership with PIs. Signpost the Therapeutic Catalyst scheme and assist the development and submission of EOI proposals. Propose translational opportunities for strategic interventional funding. Propose opportunities for consideration as TI collaborations and for experimental validation by TI's Portfolio Generation. Promote the visibility of the Network Translation team in the academic research community and life science sector. PhD or equivalent in a relevant discipline (e.g. Bioscience, Chemical Biology) with previous experience of working on oncology drug discovery in industry. You will have expertise in identifying and developing small molecule therapies and/or biotherapeutics, with an awareness of alternative therapeutic modalities. A good understanding of mechanistic cancer biology, current therapeutic approaches in oncology, and personalised medicine strategies applied to cancer treatment. A good understanding of translating opportunities from a target concept to a therapeutic, including relevant target validation methods and the use of preclinical models. Previous experience of working productively with or within the academic sector on translational/therapeutic projects. Knowledge of the broad drug development pipeline, from Target Identification through to clinical development. Excellent interpersonal skills with the ability to network and build strong working relationships. Excellent written and verbal communication skills. Strong and collaborative team player. Self-motivated individual with excellent time-management skills, able to prioritise workload and deliver to tight deadlines.Our organisation values are designed to guide all that we do. Bold: Act with ambition, courage and determination Credible: Act with rigour and professionalism Human : Act to have a positive impact on people Together: Act inclusively and collaboratively We're looking for people who can believe in and embody these organisation values and can use them to drive forward progress against our mission to beat cancer.If you're interested in applying and excited about working with us but are unsure if you have the right skills and experience, we'd still love to hear from you.We create a working environment that supports your wellbeing and provide a generous benefits package, a wide range of career and personal development opportunities and high-quality tools. Our policies and processes enable you to improve your work-life balance and take positive steps in your career.You can explore our benefits by visiting our .We operate an anonymised shortlisting process in our commitment to equality, diversity and inclusion. CVs are required for all applications; but we won't be able to view them until we invite you for an interview. Instead, we ask you to complete the work history section of the online application form for us to be able to assess you fairly and objectively.For more information on this career opportunity please or contact us at more updates on our work and careers, follow us on: and .
Data Scientist (Sports Analytics Football Focus) Were excited to be partnering with a new client a rapidly growing sports data consultancy that is extending its Data Science team. This is a fantastic opportunity to join a business at the cutting edge of football analytics, where raw data is transformed into actionable insights that drive smarter, evidence-based decisions for clubs, organisations, a click apply for full job details
Feb 15, 2026
Full time
Data Scientist (Sports Analytics Football Focus) Were excited to be partnering with a new client a rapidly growing sports data consultancy that is extending its Data Science team. This is a fantastic opportunity to join a business at the cutting edge of football analytics, where raw data is transformed into actionable insights that drive smarter, evidence-based decisions for clubs, organisations, a click apply for full job details
The science is clear - even if we do everything else right on reducing emissions, the world needs to remove 5-10 Gigatonnes of CO by 2050. At CUR8, we're on a mission to facilitate 1Bn tonnes of carbon removed in a single year. Today, for companies around the world, we are their Copilot for Carbon Removal. CUR8 is looking for a product-minded Product Engineer. You will be joining our Platform Squad. This is the team responsible for the customer-facing heart of CUR8. You will be building the "Recommendation Engine": the intelligent system that helps customers understand their emissions and builds them a perfect portfolio of carbon removal credits. Your job is to bridge the gap between complex data and a delightful user experience. You will work in a tight-knit trio with a Senior Backend Engineer and a Senior Frontend Engineer. We're small, scrappy, and ambitious, but above all, values-aligned. Our team has: Built and sold startups Advised governments on climate and net zero Published in Nature and spoken on TED stages Worked at Google, the BBC, New Scientist, and more You'll be responsible for: Shipping Features End-to-End: You will take ownership of the full feature lifecycle. This means connecting backend logic directly to the frontend UI to ensure the final result is seamless and works perfectly for the user. Building Delightful Experiences: Working with Product and Design to turn requirements into smooth, fast, and reliable interfaces. API & Logic Design: Collaborating with the team to design and implement the business logic that powers our recommendation engine. Quality & Reliability: Ensuring that what we ship is robust. This means proactively writing tests, spotting edge cases during refinement, and fixing bugs before they reach the customer. Our Tech Stack For the Platform Squad, you will be working across: Front-end: TypeScript, React, Next.js, Tailwind CSS Back-end: Go (Golang) Database: PostgreSQL Infra: Google Cloud Platform, Terraform Note: You do not need to be an expert in Go. If you are strong in TypeScript/Node or Java/Rust and willing to learn Go, we want to hear from you. About the perks: The chance to meaningfully contribute to reversing climate change Competitive salary + meaningful equity £1,000 annual learning & development budget 4 weeks/year to work from anywhere 6% pension (salary sacrifice) Regular team events, and a bright Shoreditch office A culture that respects boundaries, working parents, and different work styles Our process: We design our hiring process to be transparent, respectful, and collaborative: Intro call: 30-min chat about the role and your goals. Skills focused interviews: A take-home task (Practical coding focused on clean architecture and problem solving). A 45-min follow-up with engineers to dive deeper into your submission. Final stage: In-person (or remote), split between: Product & collaboration interview. 1:1 with a founder. CUR8 is an equal-opportunity employer. We welcome applications from people of all backgrounds, identities, and experiences, especially those underrepresented in climate and tech. Let's make climate impact inevitable. Join us.
Feb 15, 2026
Full time
The science is clear - even if we do everything else right on reducing emissions, the world needs to remove 5-10 Gigatonnes of CO by 2050. At CUR8, we're on a mission to facilitate 1Bn tonnes of carbon removed in a single year. Today, for companies around the world, we are their Copilot for Carbon Removal. CUR8 is looking for a product-minded Product Engineer. You will be joining our Platform Squad. This is the team responsible for the customer-facing heart of CUR8. You will be building the "Recommendation Engine": the intelligent system that helps customers understand their emissions and builds them a perfect portfolio of carbon removal credits. Your job is to bridge the gap between complex data and a delightful user experience. You will work in a tight-knit trio with a Senior Backend Engineer and a Senior Frontend Engineer. We're small, scrappy, and ambitious, but above all, values-aligned. Our team has: Built and sold startups Advised governments on climate and net zero Published in Nature and spoken on TED stages Worked at Google, the BBC, New Scientist, and more You'll be responsible for: Shipping Features End-to-End: You will take ownership of the full feature lifecycle. This means connecting backend logic directly to the frontend UI to ensure the final result is seamless and works perfectly for the user. Building Delightful Experiences: Working with Product and Design to turn requirements into smooth, fast, and reliable interfaces. API & Logic Design: Collaborating with the team to design and implement the business logic that powers our recommendation engine. Quality & Reliability: Ensuring that what we ship is robust. This means proactively writing tests, spotting edge cases during refinement, and fixing bugs before they reach the customer. Our Tech Stack For the Platform Squad, you will be working across: Front-end: TypeScript, React, Next.js, Tailwind CSS Back-end: Go (Golang) Database: PostgreSQL Infra: Google Cloud Platform, Terraform Note: You do not need to be an expert in Go. If you are strong in TypeScript/Node or Java/Rust and willing to learn Go, we want to hear from you. About the perks: The chance to meaningfully contribute to reversing climate change Competitive salary + meaningful equity £1,000 annual learning & development budget 4 weeks/year to work from anywhere 6% pension (salary sacrifice) Regular team events, and a bright Shoreditch office A culture that respects boundaries, working parents, and different work styles Our process: We design our hiring process to be transparent, respectful, and collaborative: Intro call: 30-min chat about the role and your goals. Skills focused interviews: A take-home task (Practical coding focused on clean architecture and problem solving). A 45-min follow-up with engineers to dive deeper into your submission. Final stage: In-person (or remote), split between: Product & collaboration interview. 1:1 with a founder. CUR8 is an equal-opportunity employer. We welcome applications from people of all backgrounds, identities, and experiences, especially those underrepresented in climate and tech. Let's make climate impact inevitable. Join us.
A leading charity in cancer research is looking for a Senior Principal Scientist to influence the direction of oncology research. The role involves working with CRUK Institutes and Centers to identify promising early-stage ideas and transform them into viable therapeutic concepts. This position requires a PhD in a relevant field and expertise in oncology drug discovery. The Senior Principal Scientist will help enhance therapeutic opportunities within a collaborative, mission-driven team in a flexible work environment.
Feb 15, 2026
Full time
A leading charity in cancer research is looking for a Senior Principal Scientist to influence the direction of oncology research. The role involves working with CRUK Institutes and Centers to identify promising early-stage ideas and transform them into viable therapeutic concepts. This position requires a PhD in a relevant field and expertise in oncology drug discovery. The Senior Principal Scientist will help enhance therapeutic opportunities within a collaborative, mission-driven team in a flexible work environment.
A leading analytical testing company in the United Kingdom is hiring for a full-time Scientist position. This role focuses on supporting product formulation development and automated testing platforms while managing client interactions and logistics. The ideal candidate will participate in quality assessments and ensure compliance with safety standards. This position demands strong organizational skills and attention to detail within a fast-paced laboratory environment.
Feb 15, 2026
Full time
A leading analytical testing company in the United Kingdom is hiring for a full-time Scientist position. This role focuses on supporting product formulation development and automated testing platforms while managing client interactions and logistics. The ideal candidate will participate in quality assessments and ensure compliance with safety standards. This position demands strong organizational skills and attention to detail within a fast-paced laboratory environment.
Go back Mid and South Essex NHS Foundation Trust Head of Radiation Protection and Diagnostic Radiology QA The closing date is 19 February 2026 We are pleased to offer an exciting opportunity to join us as the Head of Radiation Protection and Diagnostic Radiology QA. In this key role, you will act as an appointed Radiation Protection Adviser (RPA) and Medical Physics Expert (MPE) in Diagnostic Radiology, with support to external contracts as required. You will provide strategic leadership for radiation safety services across the Trust, ensuring high standards of compliance, safety, and scientific quality. Working with site leadership teams and the Deputy Director of Operations for Radiology, you will oversee the Trust's radiation protection programme and lead on all aspects of radiation safety advice. You will collaborate with senior scientists to deliver scientific and managerial leadership for services within the Trust and for partner organisations under contract. You will operate at an expert level, offering authoritative guidance on radiation legislation and national standards. Services requiring RPA/MPE support include nuclear medicine (including PET), radiopharmacy, radiotherapy, diagnostic radiology, and cardiology. MPE accreditation is essential. Applicants close to submitting an RPA portfolio may be considered within an agreed time frame. If you are an experienced leader with the vision to shape the future of radiation safety services, we welcome your application. Main duties of the job As Head of Radiation Protection and Diagnostic Radiology QA, you will: Work with Superintendent Radiographers, Department Managers and Radiation Protection Supervisors to plan and manage radiation safety audits, patient dosimetry, equipment testing, reactive investigations, optimisation projects, and the communication of findings and new guidance. Collaborate with the Physicist leading the Diagnostic Radiology QA programme and other MPEs to ensure testing meets current professional standards and national guidance. Attend external inspections, providing information, supporting discussions, and assisting with implementing recommendations. Monitor emerging regulations and assess their impact on service delivery, resources, and long term strategy for radiation protection. Develop procedures for complex radiation risk assessments, using specialist judgement to recommend strategies that minimise risk. Act as an appointed Radiation Protection Adviser (RPA) under the Ionising Radiations Regulations 2017 for the Trust and contracted organisations. Plan and coordinate Radiation Protection and Diagnostic Radiology training for staff, delivering sessions with other RPAs and MPEs. Contribute to diagnostic X ray equipment tendering and procurement, offering expert advice on specifications and performance. Lead and manage the site radiation protection programme with the Divisional Director/Designated Duty Officer for Radiology. About us Our ambition is to deliver excellent local and specialist services, to improve the health and well being of our patients, and provide a vibrant place for staff to develop, innovate and build careers. We aim to make the most of our skills and experiences so we can become the best we can be. As one organisation we will recruit the finest and retain more specialist staff due to more employment opportunities across our Trust. Job responsibilities For more information on this varied and rewarding role, please see the attached Job Description. We look forward to your application! Please be aware that we reserve the right to close the vacancy early should a high number of applications be received. Person Specification Experience Experience to act as RPA Experience as Laser Protection Advisor Experience as MRSE Qualifications Certificated MPE Certificated or soon to be RPA Disclosure and Barring Service Check This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions. Mid and South Essex NHS Foundation Trust £76,965 a year per annum (Pro Rata for Part Time)
Feb 15, 2026
Full time
Go back Mid and South Essex NHS Foundation Trust Head of Radiation Protection and Diagnostic Radiology QA The closing date is 19 February 2026 We are pleased to offer an exciting opportunity to join us as the Head of Radiation Protection and Diagnostic Radiology QA. In this key role, you will act as an appointed Radiation Protection Adviser (RPA) and Medical Physics Expert (MPE) in Diagnostic Radiology, with support to external contracts as required. You will provide strategic leadership for radiation safety services across the Trust, ensuring high standards of compliance, safety, and scientific quality. Working with site leadership teams and the Deputy Director of Operations for Radiology, you will oversee the Trust's radiation protection programme and lead on all aspects of radiation safety advice. You will collaborate with senior scientists to deliver scientific and managerial leadership for services within the Trust and for partner organisations under contract. You will operate at an expert level, offering authoritative guidance on radiation legislation and national standards. Services requiring RPA/MPE support include nuclear medicine (including PET), radiopharmacy, radiotherapy, diagnostic radiology, and cardiology. MPE accreditation is essential. Applicants close to submitting an RPA portfolio may be considered within an agreed time frame. If you are an experienced leader with the vision to shape the future of radiation safety services, we welcome your application. Main duties of the job As Head of Radiation Protection and Diagnostic Radiology QA, you will: Work with Superintendent Radiographers, Department Managers and Radiation Protection Supervisors to plan and manage radiation safety audits, patient dosimetry, equipment testing, reactive investigations, optimisation projects, and the communication of findings and new guidance. Collaborate with the Physicist leading the Diagnostic Radiology QA programme and other MPEs to ensure testing meets current professional standards and national guidance. Attend external inspections, providing information, supporting discussions, and assisting with implementing recommendations. Monitor emerging regulations and assess their impact on service delivery, resources, and long term strategy for radiation protection. Develop procedures for complex radiation risk assessments, using specialist judgement to recommend strategies that minimise risk. Act as an appointed Radiation Protection Adviser (RPA) under the Ionising Radiations Regulations 2017 for the Trust and contracted organisations. Plan and coordinate Radiation Protection and Diagnostic Radiology training for staff, delivering sessions with other RPAs and MPEs. Contribute to diagnostic X ray equipment tendering and procurement, offering expert advice on specifications and performance. Lead and manage the site radiation protection programme with the Divisional Director/Designated Duty Officer for Radiology. About us Our ambition is to deliver excellent local and specialist services, to improve the health and well being of our patients, and provide a vibrant place for staff to develop, innovate and build careers. We aim to make the most of our skills and experiences so we can become the best we can be. As one organisation we will recruit the finest and retain more specialist staff due to more employment opportunities across our Trust. Job responsibilities For more information on this varied and rewarding role, please see the attached Job Description. We look forward to your application! Please be aware that we reserve the right to close the vacancy early should a high number of applications be received. Person Specification Experience Experience to act as RPA Experience as Laser Protection Advisor Experience as MRSE Qualifications Certificated MPE Certificated or soon to be RPA Disclosure and Barring Service Check This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions. Mid and South Essex NHS Foundation Trust £76,965 a year per annum (Pro Rata for Part Time)
Full-time or Part-time: Full-Time Job Type: Employee Accelerate the possible by joining a winning Amcor team that's transforming the packaging industry and improving lives around the world. At Amcor, we unpack possibility through our innovative and responsible packaging to provide solutions that benefit our customers, our people and our planet. More than 10,000 consumers worldwide encounter our products every second and rely on us for safe access to food, medicine and other goods. We value their trust by making safety our guiding principle. It's our core value and integral to how we do business. Beyond this core principle, our shared values and behaviors unite us as we work together to elevate customers, shape lives and protect the future. We champion our customers and help them succeed. We play to win - adapting quickly in an everchanging world - and make smart choices to safeguard our business, our communities and the people we serve for generations to come. And we invest in our world class team, empowering our colleagues to unpack their potential, because we believe when our people grow, so does our business. DIVISION: Global Rigid Packaging Solutions FUNCTION: Research & Development JOB TITLE: R&D CORE Material Scientist II REPORTING TO: Director of Materials Innovation - Global Rigid Packaging Solutions R&D Core Scope: Support Global Material initiatives by assessing and developing CORE materials that align with our innovation and sustainability objectives. Manage R&D projects focused on CORE material and sustainability. Support collaboration with cross functional teams across various sectors, while remaining informed about emerging opportunities. Additionally, support external partnerships with key suppliers and process suppliers to drive the construction of future solution pipelines. About the team: The R&D team, composed of experienced professionals across multiple geographies, plays a critical role in advancing the company's innovation and sustainability goals. Their focus spans three strategic pillars: Sustainability: Implement and scale sustainable business practices across operations and the value chain, with a focus on reducing environmental impact, maximizing circularity, and enhancing long term value creation. Product Innovation: Design and develop new and improved packaging solutions that address evolving customer needs across diverse industries and applications. Cost Innovation: Drive value creation by optimizing cost structures through material efficiency, process innovation, and design simplification-while maintaining or enhancing product performance and quality. This role is pivotal in shaping the future of rigid packaging by helping to deliver transformative solutions that meet evolving customer expectations, regulatory demands, and environmental imperatives. Key Responsibilities: Lead and manage R&D projects focused on advanced material development in alignment with the company's innovation and sustainability goals, that could require new material processing. Maintain the sustainable materials innovation pipeline & related programs. Know the business well enough to understand overall market needs and to predict future needs. Collaborate with cross functional teams across Healthcare, Homecare, Food, Beverage, Beauty, and Wellness sectors to identify and implement innovative solutions. Drive the definition and early TRL exploration of new materials that enhance defined KPIs, such as PCR content, portfolio diversification, efficiency and optimization between others. Stay abreast of emerging materials and industry trends to ensure the company remains at the forefront of innovation, by taking part in fairs, conducting patents and other newsletter watch. Develop and maintain relationships with external partners, including academic institutions, research organizations, and material providers. Prepare and present technical reports, proposals, and presentations to senior management and stakeholders. Drive ongoing innovation and technology scouting activities in sustainability, particularly materials arena. Key Performance Indicators: Number of CORE material projects successfully developed and implemented. Frequency and effectiveness of collaboration meetings with cross functional teams. Improvement in energy efficiency metrics (e.g., percentage reduction in energy consumption). Number of emerging materials and industry trends integrated into R&D processes. Participation in industry fairs, patent watches, and newsletter subscriptions. Contributions from external partnerships to R&D projects (e.g., joint publications, co developed materials). Qualifications: Education: Master's Degree or PhD in materials related discipline. 4 7 years of experience in R&D, with a focus on advanced material and sustainability. Proven track record of leading successful R&D projects from concept to commercialization. Excellent leadership, communication, and project management skills. Ability to work effectively in a fast paced, dynamic environment. Experience in the Healthcare, Homecare, Food, Beverage, Beauty, or Wellness sectors is highly desirable. Experienced program leader relative to material science in a corporate setting able to define, implement, & maintain effective program management practices. Essential Functions/Skills: Must have safety awareness, dependability, clear written and oral communication. Proficient and experienced in a wide range of aspects of material science. Proficient knowledge of PET & Polyolefins and basic knowledge of alternative materials. Combines lateral/creative thinking with scientific knowledge. Working knowledge of physio chemical material behaviours such as migration and permeability. Sufficient business awareness to understand overall market needs and to predict future needs, and willingness to learn this across multiple markets and geographies. Manages multi dimensional material development programs including alignment of internal stakeholders and indirect leadership of cross functional project teams. Prescribes the use of appropriate project management & engineering tools for development & implementation of resin solutions. Internal expert regarding PCR usage and approaches/methods for increasing amount of PCR in GPRS products. Works in partnership with NPD teams and BU's to address challenges/opportunities in sustainable materials and increase PCR inclusion. Requires tact and effectiveness in dealing with a wide variety of stakeholders in everyday working relationships & executive reporting/communication. Responsible for completion of work within budget for area of responsibility. Desirable Skills: Collaborative work style exhibiting willingness to learn as well as teach/coach others. Applies professional and engineering/design principles to develop an understanding of multi dimensional, variable situations that will guide thinking about ways to address challenges and decipher relevant solutions. Strong program management skills and experience with ability to lead high priority, cross functional development programs. Proficiency with material requirements for injection, extrusion, thermoforming and blow molding processes. Proven ability to work autonomously and adds value in all phases of a project and applies analytical skills. Makes own decisions regarding how to approach specific work assignments. Holds self and others to appropriate policies and procedures. Will seek feedback and correct own performance. About Amcor Amcor is the global leader in developing and producing responsible consumer packaging and dispensing solutions across a variety of materials for nutrition, health, beauty and wellness categories. Our global product innovation and sustainability expertise enables us to solve packaging challenges around the world every day, producing a range of flexible packaging, rigid packaging, cartons and closures that are more sustainable, functional and appealing for our customers and their consumers. We are guided by our purpose of elevating customers, shaping lives and protecting the future. Supported by a commitment to safety, over 75,000 people generate $23 billion in annualized sales from operations that span over 400 locations in more than 40 countries. NYSE: AMCR; ASX: AMC LinkedIn YouTube Amcor is committed to providing a secure and reliable experience for all job seekers. If you are looking to join Amcor, please read this page to help you avoid recruitment scams. Click Here!
Feb 15, 2026
Full time
Full-time or Part-time: Full-Time Job Type: Employee Accelerate the possible by joining a winning Amcor team that's transforming the packaging industry and improving lives around the world. At Amcor, we unpack possibility through our innovative and responsible packaging to provide solutions that benefit our customers, our people and our planet. More than 10,000 consumers worldwide encounter our products every second and rely on us for safe access to food, medicine and other goods. We value their trust by making safety our guiding principle. It's our core value and integral to how we do business. Beyond this core principle, our shared values and behaviors unite us as we work together to elevate customers, shape lives and protect the future. We champion our customers and help them succeed. We play to win - adapting quickly in an everchanging world - and make smart choices to safeguard our business, our communities and the people we serve for generations to come. And we invest in our world class team, empowering our colleagues to unpack their potential, because we believe when our people grow, so does our business. DIVISION: Global Rigid Packaging Solutions FUNCTION: Research & Development JOB TITLE: R&D CORE Material Scientist II REPORTING TO: Director of Materials Innovation - Global Rigid Packaging Solutions R&D Core Scope: Support Global Material initiatives by assessing and developing CORE materials that align with our innovation and sustainability objectives. Manage R&D projects focused on CORE material and sustainability. Support collaboration with cross functional teams across various sectors, while remaining informed about emerging opportunities. Additionally, support external partnerships with key suppliers and process suppliers to drive the construction of future solution pipelines. About the team: The R&D team, composed of experienced professionals across multiple geographies, plays a critical role in advancing the company's innovation and sustainability goals. Their focus spans three strategic pillars: Sustainability: Implement and scale sustainable business practices across operations and the value chain, with a focus on reducing environmental impact, maximizing circularity, and enhancing long term value creation. Product Innovation: Design and develop new and improved packaging solutions that address evolving customer needs across diverse industries and applications. Cost Innovation: Drive value creation by optimizing cost structures through material efficiency, process innovation, and design simplification-while maintaining or enhancing product performance and quality. This role is pivotal in shaping the future of rigid packaging by helping to deliver transformative solutions that meet evolving customer expectations, regulatory demands, and environmental imperatives. Key Responsibilities: Lead and manage R&D projects focused on advanced material development in alignment with the company's innovation and sustainability goals, that could require new material processing. Maintain the sustainable materials innovation pipeline & related programs. Know the business well enough to understand overall market needs and to predict future needs. Collaborate with cross functional teams across Healthcare, Homecare, Food, Beverage, Beauty, and Wellness sectors to identify and implement innovative solutions. Drive the definition and early TRL exploration of new materials that enhance defined KPIs, such as PCR content, portfolio diversification, efficiency and optimization between others. Stay abreast of emerging materials and industry trends to ensure the company remains at the forefront of innovation, by taking part in fairs, conducting patents and other newsletter watch. Develop and maintain relationships with external partners, including academic institutions, research organizations, and material providers. Prepare and present technical reports, proposals, and presentations to senior management and stakeholders. Drive ongoing innovation and technology scouting activities in sustainability, particularly materials arena. Key Performance Indicators: Number of CORE material projects successfully developed and implemented. Frequency and effectiveness of collaboration meetings with cross functional teams. Improvement in energy efficiency metrics (e.g., percentage reduction in energy consumption). Number of emerging materials and industry trends integrated into R&D processes. Participation in industry fairs, patent watches, and newsletter subscriptions. Contributions from external partnerships to R&D projects (e.g., joint publications, co developed materials). Qualifications: Education: Master's Degree or PhD in materials related discipline. 4 7 years of experience in R&D, with a focus on advanced material and sustainability. Proven track record of leading successful R&D projects from concept to commercialization. Excellent leadership, communication, and project management skills. Ability to work effectively in a fast paced, dynamic environment. Experience in the Healthcare, Homecare, Food, Beverage, Beauty, or Wellness sectors is highly desirable. Experienced program leader relative to material science in a corporate setting able to define, implement, & maintain effective program management practices. Essential Functions/Skills: Must have safety awareness, dependability, clear written and oral communication. Proficient and experienced in a wide range of aspects of material science. Proficient knowledge of PET & Polyolefins and basic knowledge of alternative materials. Combines lateral/creative thinking with scientific knowledge. Working knowledge of physio chemical material behaviours such as migration and permeability. Sufficient business awareness to understand overall market needs and to predict future needs, and willingness to learn this across multiple markets and geographies. Manages multi dimensional material development programs including alignment of internal stakeholders and indirect leadership of cross functional project teams. Prescribes the use of appropriate project management & engineering tools for development & implementation of resin solutions. Internal expert regarding PCR usage and approaches/methods for increasing amount of PCR in GPRS products. Works in partnership with NPD teams and BU's to address challenges/opportunities in sustainable materials and increase PCR inclusion. Requires tact and effectiveness in dealing with a wide variety of stakeholders in everyday working relationships & executive reporting/communication. Responsible for completion of work within budget for area of responsibility. Desirable Skills: Collaborative work style exhibiting willingness to learn as well as teach/coach others. Applies professional and engineering/design principles to develop an understanding of multi dimensional, variable situations that will guide thinking about ways to address challenges and decipher relevant solutions. Strong program management skills and experience with ability to lead high priority, cross functional development programs. Proficiency with material requirements for injection, extrusion, thermoforming and blow molding processes. Proven ability to work autonomously and adds value in all phases of a project and applies analytical skills. Makes own decisions regarding how to approach specific work assignments. Holds self and others to appropriate policies and procedures. Will seek feedback and correct own performance. About Amcor Amcor is the global leader in developing and producing responsible consumer packaging and dispensing solutions across a variety of materials for nutrition, health, beauty and wellness categories. Our global product innovation and sustainability expertise enables us to solve packaging challenges around the world every day, producing a range of flexible packaging, rigid packaging, cartons and closures that are more sustainable, functional and appealing for our customers and their consumers. We are guided by our purpose of elevating customers, shaping lives and protecting the future. Supported by a commitment to safety, over 75,000 people generate $23 billion in annualized sales from operations that span over 400 locations in more than 40 countries. NYSE: AMCR; ASX: AMC LinkedIn YouTube Amcor is committed to providing a secure and reliable experience for all job seekers. If you are looking to join Amcor, please read this page to help you avoid recruitment scams. Click Here!
Senior RF Test Engineer St Neots (PE19) - Permanent - Onsite £45,000 - £58,000 25 days annual leave inclusive of up to 3 days Christmas shut-down Buy or sell up to 5 days annual leave Annual Wellbeing allowance Two pension schemes to choose from Private Medical Insurance + discounts for additional family members Life Assurance scheme up to 4 x salary Share Save scheme Electric/Hybrid Car leasing scheme Cycle to work scheme Retail discounts Career development support Come and join our expanding Electronic Warfare Operations Support Group (EWOS) which is made up of 60+electronic warfare specialists. From all manner of backgrounds, our engineers, scientists, and ex-military personnel combine their experience to help our customers achieve the true operational potential and help keep their people and platforms safe. We are building anew team led by our Principal RF Test Engineer at a state-of-the-art test and evaluation facility at our head office in St Neots, Cambridgeshire. You will help plan and support domestic and international trials within the facility, while working with both present and future technology. You will become a SME in the operation of software and hardware models, applying doctrinal methods to simulation scenarios. You will play a crucial part integrating, configuring and verifying performance of a wide range of components used within a laboratory environment. This will involve the generation of test programmes using a variety of test equipment. You will assist in running laboratory trials, ensuring customers can validate the performance of assets within a synthetic test environment. Working autonomously, you will be crucial to ensure the success of key projects, all whilst being supported by our on-site MASS teams. This role works closely with our customers and your knowledge and technical insights will help shape planning, development, integration, and delivery of crucial national and international synthetic trials. The invaluable experience you ll bring , to help us achieve more. Essential: Experience creating test scripts/programmes (e.g. MATLAB, Python, or LabView). Understanding of synthetic testing environments. Operation of test equipment in a laboratory environment (e.g. Oscilloscopes, Signal Generators, Spectrum/Network Analysers). Experience with Direct Signal Injection (DSI) testing. Experience of analogue and digital RF circuitry. Strong background in EW systems and concepts, including radar systems. Working autonomously and tasking junior engineers. STEM Degree or extensive relevant experience / technical aptitude. Desirable: Doctrinal experience with EW systems (e.g. radar, command and control, targeting and effectors). Experience Integration/calibration of hardware and software models into a laboratory environment. Creation of laboratory procedures. Version controlling hardware and software components. Experience working on agile projects. Experience mentoring junior engineers. Wellbeing is at the core to our culture, allowing employees to flourish and to achieve their full potential. Our people are important to us, and we take pride in our wellbeing programmes and policies that support individuals including, mental health first aiders and readily available support through our extensive employee assistance programme. Our Non-negotiables: Due to the highly secure nature of the projects that you will be involved with, you must be: A UK National and eligible to work in the UK Eligible to obtain and maintain a UK Government SC-level security clearance Apply today to see how working for MASS could work for you!
Feb 15, 2026
Full time
Senior RF Test Engineer St Neots (PE19) - Permanent - Onsite £45,000 - £58,000 25 days annual leave inclusive of up to 3 days Christmas shut-down Buy or sell up to 5 days annual leave Annual Wellbeing allowance Two pension schemes to choose from Private Medical Insurance + discounts for additional family members Life Assurance scheme up to 4 x salary Share Save scheme Electric/Hybrid Car leasing scheme Cycle to work scheme Retail discounts Career development support Come and join our expanding Electronic Warfare Operations Support Group (EWOS) which is made up of 60+electronic warfare specialists. From all manner of backgrounds, our engineers, scientists, and ex-military personnel combine their experience to help our customers achieve the true operational potential and help keep their people and platforms safe. We are building anew team led by our Principal RF Test Engineer at a state-of-the-art test and evaluation facility at our head office in St Neots, Cambridgeshire. You will help plan and support domestic and international trials within the facility, while working with both present and future technology. You will become a SME in the operation of software and hardware models, applying doctrinal methods to simulation scenarios. You will play a crucial part integrating, configuring and verifying performance of a wide range of components used within a laboratory environment. This will involve the generation of test programmes using a variety of test equipment. You will assist in running laboratory trials, ensuring customers can validate the performance of assets within a synthetic test environment. Working autonomously, you will be crucial to ensure the success of key projects, all whilst being supported by our on-site MASS teams. This role works closely with our customers and your knowledge and technical insights will help shape planning, development, integration, and delivery of crucial national and international synthetic trials. The invaluable experience you ll bring , to help us achieve more. Essential: Experience creating test scripts/programmes (e.g. MATLAB, Python, or LabView). Understanding of synthetic testing environments. Operation of test equipment in a laboratory environment (e.g. Oscilloscopes, Signal Generators, Spectrum/Network Analysers). Experience with Direct Signal Injection (DSI) testing. Experience of analogue and digital RF circuitry. Strong background in EW systems and concepts, including radar systems. Working autonomously and tasking junior engineers. STEM Degree or extensive relevant experience / technical aptitude. Desirable: Doctrinal experience with EW systems (e.g. radar, command and control, targeting and effectors). Experience Integration/calibration of hardware and software models into a laboratory environment. Creation of laboratory procedures. Version controlling hardware and software components. Experience working on agile projects. Experience mentoring junior engineers. Wellbeing is at the core to our culture, allowing employees to flourish and to achieve their full potential. Our people are important to us, and we take pride in our wellbeing programmes and policies that support individuals including, mental health first aiders and readily available support through our extensive employee assistance programme. Our Non-negotiables: Due to the highly secure nature of the projects that you will be involved with, you must be: A UK National and eligible to work in the UK Eligible to obtain and maintain a UK Government SC-level security clearance Apply today to see how working for MASS could work for you!
Principal Mechanical Engineer page is loaded Principal Mechanical Engineerremote type: Hybridlocations: Cambridgetime type: Full timeposted on: Posted 2 Days Agojob requisition id: R45925Xylem is a Fortune 500 global water solutions company dedicated to advancing sustainable impact and empowering the people who make water work every day. As a leading water technology company with 23,000 employees operating in over 150 countries, Xylem is at the forefront of addressing the world's most critical water challenges. We invite passionate individuals to join our team, dedicated to exceeding customer expectations through innovative and sustainable solutions.Sentec, a Xylem brand, seeks to hire an Principal Mechanical Engineer to lead our talented mechanical engineering skill group.As Principal, you will lead a mechanical engineering team on high-value, technically challenging projects, internal to Xylem and external clients. You will own mechanical architecture and key technical decisions and act as subject-matter expert in mechanical design, materials, and manufacturing. You will deliver innovative mechanical solutions from early concept through detailed design and industrialisation and validation testing. You will work directly with Xylem partners and external clients to understand requirements and translate them into robust engineering solutions, contribute to project planning, technical reporting and support proposal writing, technical scoping, and effort estimation.As a senior colleague, you will mentor and develop junior and mid-level engineers and scientists, foster a collaborative, high-performance engineering culture and set engineering best practice. You will also be responsible for supporting project management as well as business development activities under the guidance of the respective teams. The position is largely based in our Cambridge office however you will have the opportunity for some travel, this could be UK-wide, within Europe, the United States or the Far East. At Sentec you will be working in a rapidly evolving industry at an exciting time for technologists developing solutions in multiple sectors with a strong emphasis on sustainability. In order to be successful you will need to demonstrate leadership in pursuit of technical solutions and novel ideas, have a hands-on approach to problem solving and ultimately managing projects against time, budget and client expectations. This role combines hands-on engineering, technical decision-making, project and team leadership within a fast-paced consultancy environment spanning multiple sectors, working towards deadlines and delivering excellent technical solutions. You will be required to communicate effectively in a wide range of environments, both with colleagues and clients and will have the opportunity to develop your negotiation skills and expand your technical knowledge. Minimum Qualifications: Education, Experience, Skills, Abilities, License/Certification: Extensive experience (10+ years) in mechanical engineering / product development Experience in people leadership, preferably in mechanical engineering Strong 3D CAD capability (principally Creo but SolidWorks also advantageous) Proven experience taking products from concept to manufacture Hands-on experience making parts and building prototypes Experience dealing with 3rd party suppliers such as engineering workshops, plastic fabricators, hardware suppliers Excellent understanding of materials, tolerancing, and manufacturing processes Experience working in multidisciplinary teams (physics, electronics, software) Minimum 2/1 Degree (or equivalent) in Mechanical Engineering or related discipline Desirable Skills/Knowledge: Background in consultancy or contract R&D environments Experience with machinery such as lathes and milling machines Experience with 3D printing, both internal and bureau Experience in one or more sectors such as: Sensing technology such as optical, magnetic, ultrasonic Consumer and industrial products Scientific instrumentation Water infrastructure Sustainable energy Knowledge of regulatory or quality systems (e.g. ISO 13485, ISO 9001) Experience with FEA, thermal analysis, or other simulation Physical Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Regularly required to sit or stand, reach, bend and move about the facility Work Environment: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Office: Standard office equipment; work usually performed in an office or site laboratory setting Estimated 10 % or less travel requirement Standard weekly job hours: 37.5 hours Benefits Include: Competitive salaries Holiday of 25 days per year, increases with length of service Group life cover at 4 times basic salary Private health care Salary sacrifice pension scheme Relocation expenses as appropriate Annual performance and merit process Discretionary 10% All staff bonus scheme Employee referral bonus scheme Access to flexible benefits including cycle to work, critical illness cover and green car leasing Flexible and remote workingJoin the global Xylem team to be a part of innovative technology solutions transforming water usage, conservation, and re-use. Our products impact public utilities, industrial sectors, residential areas, and commercial buildings, with a commitment to providing smart metering, network technologies, and advanced analytics for water, electric, and gas utilities. Partner with us in creating a world where water challenges are met with ingenuity and dedication; where we recognize the power of inclusion and belonging in driving innovation and allowing us to compete more effectively around the world.background, skills and interests.
Feb 15, 2026
Full time
Principal Mechanical Engineer page is loaded Principal Mechanical Engineerremote type: Hybridlocations: Cambridgetime type: Full timeposted on: Posted 2 Days Agojob requisition id: R45925Xylem is a Fortune 500 global water solutions company dedicated to advancing sustainable impact and empowering the people who make water work every day. As a leading water technology company with 23,000 employees operating in over 150 countries, Xylem is at the forefront of addressing the world's most critical water challenges. We invite passionate individuals to join our team, dedicated to exceeding customer expectations through innovative and sustainable solutions.Sentec, a Xylem brand, seeks to hire an Principal Mechanical Engineer to lead our talented mechanical engineering skill group.As Principal, you will lead a mechanical engineering team on high-value, technically challenging projects, internal to Xylem and external clients. You will own mechanical architecture and key technical decisions and act as subject-matter expert in mechanical design, materials, and manufacturing. You will deliver innovative mechanical solutions from early concept through detailed design and industrialisation and validation testing. You will work directly with Xylem partners and external clients to understand requirements and translate them into robust engineering solutions, contribute to project planning, technical reporting and support proposal writing, technical scoping, and effort estimation.As a senior colleague, you will mentor and develop junior and mid-level engineers and scientists, foster a collaborative, high-performance engineering culture and set engineering best practice. You will also be responsible for supporting project management as well as business development activities under the guidance of the respective teams. The position is largely based in our Cambridge office however you will have the opportunity for some travel, this could be UK-wide, within Europe, the United States or the Far East. At Sentec you will be working in a rapidly evolving industry at an exciting time for technologists developing solutions in multiple sectors with a strong emphasis on sustainability. In order to be successful you will need to demonstrate leadership in pursuit of technical solutions and novel ideas, have a hands-on approach to problem solving and ultimately managing projects against time, budget and client expectations. This role combines hands-on engineering, technical decision-making, project and team leadership within a fast-paced consultancy environment spanning multiple sectors, working towards deadlines and delivering excellent technical solutions. You will be required to communicate effectively in a wide range of environments, both with colleagues and clients and will have the opportunity to develop your negotiation skills and expand your technical knowledge. Minimum Qualifications: Education, Experience, Skills, Abilities, License/Certification: Extensive experience (10+ years) in mechanical engineering / product development Experience in people leadership, preferably in mechanical engineering Strong 3D CAD capability (principally Creo but SolidWorks also advantageous) Proven experience taking products from concept to manufacture Hands-on experience making parts and building prototypes Experience dealing with 3rd party suppliers such as engineering workshops, plastic fabricators, hardware suppliers Excellent understanding of materials, tolerancing, and manufacturing processes Experience working in multidisciplinary teams (physics, electronics, software) Minimum 2/1 Degree (or equivalent) in Mechanical Engineering or related discipline Desirable Skills/Knowledge: Background in consultancy or contract R&D environments Experience with machinery such as lathes and milling machines Experience with 3D printing, both internal and bureau Experience in one or more sectors such as: Sensing technology such as optical, magnetic, ultrasonic Consumer and industrial products Scientific instrumentation Water infrastructure Sustainable energy Knowledge of regulatory or quality systems (e.g. ISO 13485, ISO 9001) Experience with FEA, thermal analysis, or other simulation Physical Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Regularly required to sit or stand, reach, bend and move about the facility Work Environment: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Office: Standard office equipment; work usually performed in an office or site laboratory setting Estimated 10 % or less travel requirement Standard weekly job hours: 37.5 hours Benefits Include: Competitive salaries Holiday of 25 days per year, increases with length of service Group life cover at 4 times basic salary Private health care Salary sacrifice pension scheme Relocation expenses as appropriate Annual performance and merit process Discretionary 10% All staff bonus scheme Employee referral bonus scheme Access to flexible benefits including cycle to work, critical illness cover and green car leasing Flexible and remote workingJoin the global Xylem team to be a part of innovative technology solutions transforming water usage, conservation, and re-use. Our products impact public utilities, industrial sectors, residential areas, and commercial buildings, with a commitment to providing smart metering, network technologies, and advanced analytics for water, electric, and gas utilities. Partner with us in creating a world where water challenges are met with ingenuity and dedication; where we recognize the power of inclusion and belonging in driving innovation and allowing us to compete more effectively around the world.background, skills and interests.
Lead Data Scientist - eCommerce Leicester, UK (Hybrid) Up to £75,000 DOE iO Associates are aligned with one of the UK's most recognised and fast-scaling retail powerhouses, operating at significant scale within a highly data-driven eCommerce environment where analytics directly shapes commercial performance click apply for full job details
Feb 15, 2026
Full time
Lead Data Scientist - eCommerce Leicester, UK (Hybrid) Up to £75,000 DOE iO Associates are aligned with one of the UK's most recognised and fast-scaling retail powerhouses, operating at significant scale within a highly data-driven eCommerce environment where analytics directly shapes commercial performance click apply for full job details
The Association of Technology, Management and Applied Engineering
Overview Director, MIDD AI/ML Scientist Clinical Pharmacology Quantitative Medicine (CPQM) is accountable for applying clinical pharmacology strategies and the principles of quantitative medicine across RIIRU (Respiratory, Immunology & Inflammation Research Unit) to enable end-to-end development of transformative medicines. A key component of the CPQM mission is to harness AI/ML and mechanistic modelling to drive robust Development Strategies including dose, endpoint and population selection; smart clinical trials and Model Informed Drug Development (MIDD) evidence. Hybrid AIML-Pharmacometrics/QSP methodologies combine AI/ML with mechanistic modelling to integrate novel data types (e.g., imaging, biomarkers, OMICs, digital endpoints, real-world data) for predictive and impactful decision-making. This role focuses on the practical application of emerging AI/ML and hybrid AI/ML-Pharmacometrics methodologies to projects at asset and disease levels, supporting a wide range of clinical development decisions across RIIRU. The role involves collaborating with Clinical Pharmacology leads and cross-functional teams to integrate diverse biomedical data (clinical, imaging, biomarkers, OMICs, digital health, real-world data) into hybrid AI/ML-Pharmacometrics approaches, direct stakeholder engagement, identifying high-impact opportunities, analysis planning, execution, interpretation and communication of results and impact. This position is an excellent entry point for experienced quantitative scientists with a background in AI/ML (e.g., PhDs in AI/ML or related fields), drug development and Pharmacometrics/QSP seeking to apply those techniques to benefit patients at the frontier of medicine. We create a place where people can grow, be their best, be safe, and feel welcome, valued and included. We offer a competitive salary, an annual bonus based on company performance, healthcare and wellbeing programmes, pension plan membership, and shares and savings programme. We embrace modern work practises; our Performance with Choice programme offers a hybrid working model, empowering you to find the optimal balance between remote and in-office work. Discover more about our company wide benefits and life at GSK on our webpage Life at GSK GSK. In this role you will Manage stakeholder engagement: Proactively interact with stakeholders, line and middle management, staff and external contacts on a functional and tactical level. Identify high impact opportunities for hybrid AI/ML-pharmacometrics approaches on projects. Execute portfolio projects: Apply AI/ML and hybrid AI/ML-pharmacometrics approaches to deliver analyses that inform drug development decisions (dose, regimen, endpoint, population, trial design). Work cross-functionally: Collaborate with CPMS leads, QSP modellers, statisticians, and digital/imaging experts to integrate AI/ML analyses with existing modelling frameworks. Develop analysis plans, conduct analyses and communicate interim/final results. Contribute to our capabilities: Engage with academic groups and external vendors supporting joint internal-external projects. Identify best practices and disseminate learnings from internal and external sources. Drive awareness: Deliver training, seminars, and internal communications to increase literacy in AI/ML-pharmacometrics across CPQM and RIIRU. Have external influence: Conference presentations, posters, and publications in scientific journals to represent GSK's impact in AI/ML for drug development. Why you Basic Qualifications & Skills We are looking for a professional with these required skills to achieve our goals: PhD (or equivalent) in AI/ML or related quantitative fields or in Life Sciences. Strong foundation and experience in building and applying AI/ML models. Strong foundation and experience in statistics and/or pharmacometrics / quantitative clinical pharmacology. Strong industry drug development experience, working within teams. Experience coding AI/ML pipelines in Python/PyTorch or Julia/Pumas. Strong interest and experience in promoting hybrid AI/ML-pharmacometrics expertise. Developing people and processes. Excellent collaboration and communication skills (written, verbal and presentation), with experience working in interdisciplinary teams. Preferred Qualifications & Skills If you have the following characteristics, it would be a plus: Direct pharmacometric project experience. Direct experience applying AIML approaches for longitudinal data and/or SciML approaches. Familiarity with the application of agentic AI to enhance novel process integration. Salary and benefits LI-GSK# The annual base salary for new hires in this position ranges from $188,100 to $313,500 for certain US locations. This reflects base salary ranges and may vary by location, skills, experience, and market. The position offers an annual bonus and eligibility to participate in a share-based long-term incentive program. Benefits include health care and other insurance, retirement benefits, paid holidays, vacation, and paid caregiver/parental and medical leave. GSK is an Equal Opportunity Employer. This includes equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information, military service or any basis prohibited by law. We support flexible and agile working arrangements where possible. If adjustments are needed to participate in the process, contact us at to request assistance. For questions not related to adjustments, please refer to our Recruitment FAQ guide. Important notice to Employment businesses/ Agencies: GSK does not accept referrals from employment businesses or agencies without prior written authorization. This ensures appropriate contractual arrangements are in place prior to referring candidates. For US regulatory transparency, GSK may capture and report certain expenses on your behalf if you are interviewed, in compliance with applicable laws. More information is available via CMS guidelines.
Feb 15, 2026
Full time
Overview Director, MIDD AI/ML Scientist Clinical Pharmacology Quantitative Medicine (CPQM) is accountable for applying clinical pharmacology strategies and the principles of quantitative medicine across RIIRU (Respiratory, Immunology & Inflammation Research Unit) to enable end-to-end development of transformative medicines. A key component of the CPQM mission is to harness AI/ML and mechanistic modelling to drive robust Development Strategies including dose, endpoint and population selection; smart clinical trials and Model Informed Drug Development (MIDD) evidence. Hybrid AIML-Pharmacometrics/QSP methodologies combine AI/ML with mechanistic modelling to integrate novel data types (e.g., imaging, biomarkers, OMICs, digital endpoints, real-world data) for predictive and impactful decision-making. This role focuses on the practical application of emerging AI/ML and hybrid AI/ML-Pharmacometrics methodologies to projects at asset and disease levels, supporting a wide range of clinical development decisions across RIIRU. The role involves collaborating with Clinical Pharmacology leads and cross-functional teams to integrate diverse biomedical data (clinical, imaging, biomarkers, OMICs, digital health, real-world data) into hybrid AI/ML-Pharmacometrics approaches, direct stakeholder engagement, identifying high-impact opportunities, analysis planning, execution, interpretation and communication of results and impact. This position is an excellent entry point for experienced quantitative scientists with a background in AI/ML (e.g., PhDs in AI/ML or related fields), drug development and Pharmacometrics/QSP seeking to apply those techniques to benefit patients at the frontier of medicine. We create a place where people can grow, be their best, be safe, and feel welcome, valued and included. We offer a competitive salary, an annual bonus based on company performance, healthcare and wellbeing programmes, pension plan membership, and shares and savings programme. We embrace modern work practises; our Performance with Choice programme offers a hybrid working model, empowering you to find the optimal balance between remote and in-office work. Discover more about our company wide benefits and life at GSK on our webpage Life at GSK GSK. In this role you will Manage stakeholder engagement: Proactively interact with stakeholders, line and middle management, staff and external contacts on a functional and tactical level. Identify high impact opportunities for hybrid AI/ML-pharmacometrics approaches on projects. Execute portfolio projects: Apply AI/ML and hybrid AI/ML-pharmacometrics approaches to deliver analyses that inform drug development decisions (dose, regimen, endpoint, population, trial design). Work cross-functionally: Collaborate with CPMS leads, QSP modellers, statisticians, and digital/imaging experts to integrate AI/ML analyses with existing modelling frameworks. Develop analysis plans, conduct analyses and communicate interim/final results. Contribute to our capabilities: Engage with academic groups and external vendors supporting joint internal-external projects. Identify best practices and disseminate learnings from internal and external sources. Drive awareness: Deliver training, seminars, and internal communications to increase literacy in AI/ML-pharmacometrics across CPQM and RIIRU. Have external influence: Conference presentations, posters, and publications in scientific journals to represent GSK's impact in AI/ML for drug development. Why you Basic Qualifications & Skills We are looking for a professional with these required skills to achieve our goals: PhD (or equivalent) in AI/ML or related quantitative fields or in Life Sciences. Strong foundation and experience in building and applying AI/ML models. Strong foundation and experience in statistics and/or pharmacometrics / quantitative clinical pharmacology. Strong industry drug development experience, working within teams. Experience coding AI/ML pipelines in Python/PyTorch or Julia/Pumas. Strong interest and experience in promoting hybrid AI/ML-pharmacometrics expertise. Developing people and processes. Excellent collaboration and communication skills (written, verbal and presentation), with experience working in interdisciplinary teams. Preferred Qualifications & Skills If you have the following characteristics, it would be a plus: Direct pharmacometric project experience. Direct experience applying AIML approaches for longitudinal data and/or SciML approaches. Familiarity with the application of agentic AI to enhance novel process integration. Salary and benefits LI-GSK# The annual base salary for new hires in this position ranges from $188,100 to $313,500 for certain US locations. This reflects base salary ranges and may vary by location, skills, experience, and market. The position offers an annual bonus and eligibility to participate in a share-based long-term incentive program. Benefits include health care and other insurance, retirement benefits, paid holidays, vacation, and paid caregiver/parental and medical leave. GSK is an Equal Opportunity Employer. This includes equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information, military service or any basis prohibited by law. We support flexible and agile working arrangements where possible. If adjustments are needed to participate in the process, contact us at to request assistance. For questions not related to adjustments, please refer to our Recruitment FAQ guide. Important notice to Employment businesses/ Agencies: GSK does not accept referrals from employment businesses or agencies without prior written authorization. This ensures appropriate contractual arrangements are in place prior to referring candidates. For US regulatory transparency, GSK may capture and report certain expenses on your behalf if you are interviewed, in compliance with applicable laws. More information is available via CMS guidelines.
Research Engineer The Role We are seeking an experienced and motivated engineer or scientist to support the development of low Technology Readiness Level (TRL) research concepts. This role involves designing, building, testing and analysing prototype systems so they can be evaluated for future capability click apply for full job details
Feb 14, 2026
Full time
Research Engineer The Role We are seeking an experienced and motivated engineer or scientist to support the development of low Technology Readiness Level (TRL) research concepts. This role involves designing, building, testing and analysing prototype systems so they can be evaluated for future capability click apply for full job details
A biotechnology company in Oxford is seeking a Senior Scientist I for Analytical Development & Validation. The role involves conducting and designing experimental investigations, oversight of assay development, and leading investigational projects. Ideal candidates will have significant experience in chromatographic methods and a background in a biopharmaceutical laboratory. A BSc. or MSc. in a related discipline is essential, with a PhD being desirable.
Feb 14, 2026
Full time
A biotechnology company in Oxford is seeking a Senior Scientist I for Analytical Development & Validation. The role involves conducting and designing experimental investigations, oversight of assay development, and leading investigational projects. Ideal candidates will have significant experience in chromatographic methods and a background in a biopharmaceutical laboratory. A BSc. or MSc. in a related discipline is essential, with a PhD being desirable.
Job Details: Senior Scientist I - Analytical Development & Validation Full details of the job. Vacancy Name Vacancy Name Senior Scientist I - Analytical Development & Validation Vacancy No Vacancy No VN627 Employment Type Employment Type Permanent Location of role Location of role Oxford, UK Department Department CMC Key Responsibilities To conduct and design experimental investigations enabling the advancement of the Company pipeline, process, or technology capabilities, proposing improvements for consideration by colleagues and managers. To perform assay development and qualification for ImmTAX and other TCR based molecules and oversee method transfers to CDMOs. Designing and conducting chromatographic, electrophoretic and immunoassay development studies to support stability and release of ImmTAC and other TCR based molecules. Supporting qualification of chromatographic, electrophoretic and immunoassay methods (according to ICH guidelines) to allow release testing of the company drug molecules. Contributing to method transfers to contract development and manufacturing organisations (CDMO). Leading investigational, CMC supportive packages and comparability studies of biologics/drug products. Writing study protocols and reports. Independently testing and, increasingly, leading lines of investigation. Proposing new experiments based on emerging data and other related information. Providing support on technical aspects to others. Priorities: establishing priorities for own work and team-based projects; making decisions on prioritisation based on the overall goals of the team, department and project, using direct evidence and personal experience as guidance. Technical Knowledge: sharing knowledge with the wider team and, across departments representing the department both internally and externally. May also act as a mentor or manager to other colleagues, especially new hires, sharing scientific and company knowledge. Increasingly providing analysis of new techniques and theories from outside the Company to advance the way the company works; sharing these with leaders across the Company. Laboratory records: ensuring that all records and information are up to date, on time and recorded to the correct standard. Supporting and encouraging others to achieve this. Laboratory equipment: providing technical guidance to others within the team on how to use equipment most effectively; making recommendations regarding acquisition of new pieces of equipment. Reporting: communicating and presenting research findings at meetings with colleagues, senior management and partners. Adhere to safe working practices in laboratories according to Immunocore EHS policies. Person Specification Experience & knowledge Essential Experience in development of chromatographic and electrophoretic methods used in the analysis of recombinant proteins or antibodies. Worked in a bench-based biopharmaceutical laboratory environment. Established as an expert amongst peers in one or more of the following areas: electrophoretic, chromatographic, immuno-analytical. Experienced in assay qualification/validation and/ or system suitability i.e. robustness analytical limits. Familiar with biopharmaceutical stability study principles and interpretation thereof. Worked and contributed actively in a diverse team environment. Proposed and driven changes in working practices that have improved efficiency, supported teams through adoption and change. Presented detailed scientific findings and papers to internal and external audiences. Mentored and coached less experienced colleagues in scientific practices and theory. Desirable Experience with late stage/commercial biopharmaceutical assay development and characterisation. Familiar with the principles of Good Manufacturing Practise (GMP). Presented papers at external conferences. Participated in external scientific experiments and/or analytical collaborations. Led a small project team, formally or informally, through a change in practice including project management. Understanding of analytical requirements to support materials for use in clinical trials. Education & qualifications Essential: BSc. Or MSc. in biochemistry, biotechnology or related discipline. Desirable: PhD in related discipline. About the Company Immunocore (NASDAQ: IMCR) is a pioneering, commercial-stage T cell receptor biotechnology company whose purpose is to develop and commercialize a new generation of transformative medicines which address unmet patient needs in oncology, infectious diseases and autoimmune disease. Our leaders in R&D are internationally recognised as some of the biotech industry's most successful drug developers. We are creating not just an environment where great minds can interact but an innovation powerhouse answering the big questions. Focused on delivering first-in-class biological therapies to patients, we have developed a highly innovative soluble TCR platform. Our ImmTAX molecules underpin a new generation of precision engineered drugs that harness the immune system to treat a broad spectrum of diseases with high unmet medical need, including oncology, infectious diseases and autoimmune diseases. At Immunocore, we recognize that our employees are our greatest asset. We value the unique contributions each person brings to our team. By embracing Science, Trust, Respect, Integrity, Diversity, and Entrepreneurship (STRIDE), we create an environment where collaboration thrives, ideas flourish, and transformative changes happen. STRIDE represents more than just letters; it embodies our shared identity and drives our mission. We are dedicated to developing breakthrough therapies that transform patients' lives, advancing medicine, and supporting one another in these pursuits. Immunocore is proud to be an equal opportunity employer. As such, we are committed to fostering an inclusive workplace where everyone feels valued, respected, and empowered. We encourage applications from individuals of all backgrounds, regardless of race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, or any other characteristic protected by law.
Feb 14, 2026
Full time
Job Details: Senior Scientist I - Analytical Development & Validation Full details of the job. Vacancy Name Vacancy Name Senior Scientist I - Analytical Development & Validation Vacancy No Vacancy No VN627 Employment Type Employment Type Permanent Location of role Location of role Oxford, UK Department Department CMC Key Responsibilities To conduct and design experimental investigations enabling the advancement of the Company pipeline, process, or technology capabilities, proposing improvements for consideration by colleagues and managers. To perform assay development and qualification for ImmTAX and other TCR based molecules and oversee method transfers to CDMOs. Designing and conducting chromatographic, electrophoretic and immunoassay development studies to support stability and release of ImmTAC and other TCR based molecules. Supporting qualification of chromatographic, electrophoretic and immunoassay methods (according to ICH guidelines) to allow release testing of the company drug molecules. Contributing to method transfers to contract development and manufacturing organisations (CDMO). Leading investigational, CMC supportive packages and comparability studies of biologics/drug products. Writing study protocols and reports. Independently testing and, increasingly, leading lines of investigation. Proposing new experiments based on emerging data and other related information. Providing support on technical aspects to others. Priorities: establishing priorities for own work and team-based projects; making decisions on prioritisation based on the overall goals of the team, department and project, using direct evidence and personal experience as guidance. Technical Knowledge: sharing knowledge with the wider team and, across departments representing the department both internally and externally. May also act as a mentor or manager to other colleagues, especially new hires, sharing scientific and company knowledge. Increasingly providing analysis of new techniques and theories from outside the Company to advance the way the company works; sharing these with leaders across the Company. Laboratory records: ensuring that all records and information are up to date, on time and recorded to the correct standard. Supporting and encouraging others to achieve this. Laboratory equipment: providing technical guidance to others within the team on how to use equipment most effectively; making recommendations regarding acquisition of new pieces of equipment. Reporting: communicating and presenting research findings at meetings with colleagues, senior management and partners. Adhere to safe working practices in laboratories according to Immunocore EHS policies. Person Specification Experience & knowledge Essential Experience in development of chromatographic and electrophoretic methods used in the analysis of recombinant proteins or antibodies. Worked in a bench-based biopharmaceutical laboratory environment. Established as an expert amongst peers in one or more of the following areas: electrophoretic, chromatographic, immuno-analytical. Experienced in assay qualification/validation and/ or system suitability i.e. robustness analytical limits. Familiar with biopharmaceutical stability study principles and interpretation thereof. Worked and contributed actively in a diverse team environment. Proposed and driven changes in working practices that have improved efficiency, supported teams through adoption and change. Presented detailed scientific findings and papers to internal and external audiences. Mentored and coached less experienced colleagues in scientific practices and theory. Desirable Experience with late stage/commercial biopharmaceutical assay development and characterisation. Familiar with the principles of Good Manufacturing Practise (GMP). Presented papers at external conferences. Participated in external scientific experiments and/or analytical collaborations. Led a small project team, formally or informally, through a change in practice including project management. Understanding of analytical requirements to support materials for use in clinical trials. Education & qualifications Essential: BSc. Or MSc. in biochemistry, biotechnology or related discipline. Desirable: PhD in related discipline. About the Company Immunocore (NASDAQ: IMCR) is a pioneering, commercial-stage T cell receptor biotechnology company whose purpose is to develop and commercialize a new generation of transformative medicines which address unmet patient needs in oncology, infectious diseases and autoimmune disease. Our leaders in R&D are internationally recognised as some of the biotech industry's most successful drug developers. We are creating not just an environment where great minds can interact but an innovation powerhouse answering the big questions. Focused on delivering first-in-class biological therapies to patients, we have developed a highly innovative soluble TCR platform. Our ImmTAX molecules underpin a new generation of precision engineered drugs that harness the immune system to treat a broad spectrum of diseases with high unmet medical need, including oncology, infectious diseases and autoimmune diseases. At Immunocore, we recognize that our employees are our greatest asset. We value the unique contributions each person brings to our team. By embracing Science, Trust, Respect, Integrity, Diversity, and Entrepreneurship (STRIDE), we create an environment where collaboration thrives, ideas flourish, and transformative changes happen. STRIDE represents more than just letters; it embodies our shared identity and drives our mission. We are dedicated to developing breakthrough therapies that transform patients' lives, advancing medicine, and supporting one another in these pursuits. Immunocore is proud to be an equal opportunity employer. As such, we are committed to fostering an inclusive workplace where everyone feels valued, respected, and empowered. We encourage applications from individuals of all backgrounds, regardless of race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, or any other characteristic protected by law.
Alexander Edward James Consulting Limited
City, London
Remote based Reporting Line - CTO Direct Reports - None Key Stakeholder Relationships - Product owners, software developers, testers, delivery managers, professional services teams, and technical architects Role Purpose Working as part of an Agile technology team within a fast growing SaaS organisation, the Data Specialist / Data Scientist will be responsible for designing, developing, and deploying da click apply for full job details
Feb 14, 2026
Full time
Remote based Reporting Line - CTO Direct Reports - None Key Stakeholder Relationships - Product owners, software developers, testers, delivery managers, professional services teams, and technical architects Role Purpose Working as part of an Agile technology team within a fast growing SaaS organisation, the Data Specialist / Data Scientist will be responsible for designing, developing, and deploying da click apply for full job details
A global packaging leader is seeking an R&D CORE Material Scientist II to manage R&D projects in advanced materials focusing on innovation and sustainability. Candidates should possess a Master's or PhD in a materials-related discipline and 4-7 years of relevant experience. Strong leadership, communication, and project management skills are essential. The position involves collaboration with multiple sectors to drive transformative solutions that meet customer expectations and regulatory demands.
Feb 14, 2026
Full time
A global packaging leader is seeking an R&D CORE Material Scientist II to manage R&D projects in advanced materials focusing on innovation and sustainability. Candidates should possess a Master's or PhD in a materials-related discipline and 4-7 years of relevant experience. Strong leadership, communication, and project management skills are essential. The position involves collaboration with multiple sectors to drive transformative solutions that meet customer expectations and regulatory demands.
Unfortunately, we are unable to offer visa sponsorship for this role. This is a fulltime, permanent position, working a flexible 37.5 hour week, Monday - Friday. The purpose of this role is to support the development of new product formulations providing support to the automated equipment and analytical equipment. Additionally, the scientist also has the potential to support further automated platforms and health care product development evaluation. Job Responsibilities Organisation, Scheduling and Planning of Routine requests from multiple client facilities to be progressed in the client facility, utilising various automated platforms. Review Design of Experiments and progress automated runs. Support automated formulation platforms with a good level of proficiency. Manage Logistics, COSHH, Safety for routine requests from different client areas ensuring sample integrity, project timelines and demands are met. Run and Report any routine requests on automated equipment (including Statistics). Conduct associated in-line / off-line product quality assessment of Haircare products assessing damage, deposition, sensory and hair array (combing / texture). For hair fibre assessing physical assessments including torsion, tension, bending, swelling and contact angle and for Sub Fibre, assessment utilising DSC, DVS, DMA and TGA as well as analytical support utilising Raman Spectroscopy and SEM. Additional measurement support including preparation and operation of measurement tools. Maintain clear, concise and effective communication with the Key client Contacts and designees throughout the period of service. Ensure all pre-calibration of equipment is conducted. Escalate issues in a timely manner to ensure prompt resolution so as to maintain project schedule adherence. Report and document any issues or non-conformances to the relevant client contact. Assist in the preparation and review and revision of area documentation e.g. SOP's, Reports, Protocols. To ensure that all documentation is carried out on time, is accurate and legible and conforms to the relevant quality standards. Attend regular client/Eurofins team meetings. Deal with customer queries and contact designated personnel, with appropriate support from Group Leader, with any relevant information or issues relating to results or the service in general. To keep the laboratory areas clean and tidy in both 'seen' and 'unseen' areas. To have a clear understanding of the customer relationship and service goals. Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and the environment safer, healthier and more sustainable. From the food you eat to the medicines you rely on, Eurofins works with the biggest companies in
Feb 14, 2026
Full time
Unfortunately, we are unable to offer visa sponsorship for this role. This is a fulltime, permanent position, working a flexible 37.5 hour week, Monday - Friday. The purpose of this role is to support the development of new product formulations providing support to the automated equipment and analytical equipment. Additionally, the scientist also has the potential to support further automated platforms and health care product development evaluation. Job Responsibilities Organisation, Scheduling and Planning of Routine requests from multiple client facilities to be progressed in the client facility, utilising various automated platforms. Review Design of Experiments and progress automated runs. Support automated formulation platforms with a good level of proficiency. Manage Logistics, COSHH, Safety for routine requests from different client areas ensuring sample integrity, project timelines and demands are met. Run and Report any routine requests on automated equipment (including Statistics). Conduct associated in-line / off-line product quality assessment of Haircare products assessing damage, deposition, sensory and hair array (combing / texture). For hair fibre assessing physical assessments including torsion, tension, bending, swelling and contact angle and for Sub Fibre, assessment utilising DSC, DVS, DMA and TGA as well as analytical support utilising Raman Spectroscopy and SEM. Additional measurement support including preparation and operation of measurement tools. Maintain clear, concise and effective communication with the Key client Contacts and designees throughout the period of service. Ensure all pre-calibration of equipment is conducted. Escalate issues in a timely manner to ensure prompt resolution so as to maintain project schedule adherence. Report and document any issues or non-conformances to the relevant client contact. Assist in the preparation and review and revision of area documentation e.g. SOP's, Reports, Protocols. To ensure that all documentation is carried out on time, is accurate and legible and conforms to the relevant quality standards. Attend regular client/Eurofins team meetings. Deal with customer queries and contact designated personnel, with appropriate support from Group Leader, with any relevant information or issues relating to results or the service in general. To keep the laboratory areas clean and tidy in both 'seen' and 'unseen' areas. To have a clear understanding of the customer relationship and service goals. Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and the environment safer, healthier and more sustainable. From the food you eat to the medicines you rely on, Eurofins works with the biggest companies in
Senior Principal Scientist (Project Enablement) under the leadership of Agnes Martin £58,400 - £76,000 plusbenefits (includes up to 12% pension contribution and income protection) Reports to: Associate Director, Mechanistic Pharmacology Directorate: Research & Innovation Contract: Permanent Hours: Full time 35 hours per week (4 day week would be considered) Location: Cambridge, Babraham Research Campus (minimum 3 days on site) Closing date: Open until filled. We will be shortlisting on a rolling basis and will close the vacancy once we have received sufficient applications This vacancy may close earlier if a high volume of applications is received or once a suitable candidate is found, therefore we strongly recommend that you apply early to avoid disappointment. Please let us know if there is anything or as soon as possible.in particular if there are any changes or adjustments that would make it easier for you to apply. Please contact or as soon as possible. Visa sponsorship: Cancer Research UK can consider visa sponsorship for this vacancy. If this applies to you, please ensure that this is clearly marked on your application. Recruitment process: 1st stage Teams technical and competency based itnerview, 2nd stage in person interview including pre prepared presentation At Cancer Research UK, we exist to beat cancer. We are looking for a passionate and dedicated scientific professional with extensive experience in pre-clinical drug discovery in an industrial setting. As the world's biggest medical research charity, we've helped bring eleven new cancer drugs to market. However, there is still an urgent need to bring more effective treatments to patients faster. We have developed a new approach to driving therapeutic innovation through the creation of Cancer Research Horizons (CRH). We have brought together Cancer Research UK's established drug discovery teams under one organisation and leadership team, combining our unique pipeline of cancer biology expertise and access to CRUK's world-class academic network, cutting edge technology platforms and clinical expertise to 1) bring new treatments to patients faster and 2) tackle the biggest challenges in discovering cancer drugs by seeking out more radical ideas and embracing risk in our bid to achieve success. Based at sites in Cambridge, the CRUK Scotland Institute in Glasgow, and Newcastle University, Cancer Research Horizons employs 200 staff from both industrial and academic backgrounds What will I be doing? Our strategy sets out to bring deeper mechanistic understanding at the molecular and cellular level to all stages of projects, from idea to pre-clinical candidate. In this role, you will define the vision and strategy for CRH early project enablement, establishing robust processes to select and advance promising targets into the drug discovery portfolio. You will lead and develop a matrixed team, guiding them to deliver clear go/no-go decisions through deep expertise in target feasibility and druggability. You will work closely with the Portfolio Generation team to build a sustainable pipeline, evaluating risks, shaping mitigation strategies, and ensuring projects progress efficiently toward pre-clinical development. In addition, you will provide leadership within the broader CRH TI organisation, shaping strategic direction and driving scientific and technical innovation, including championing new modalities. Key accountabilities include: Provide deep expertise in assessing target feasibility, including, but not limited to, reagent generation, mechanistic characterisation, ligandability, druggability. Work at the intersection between portfolio generation, molecular sciences, chemistry and biosciences to define and prosecute strategies that deliver clear, early go/no-go decisions across a range of challenging target classes. Provide Scientific and Strategic leadership for the assessment of novel targets and mechanisms, to drive innovation and portfolio success. Communicate effectively, to influence multiple stakeholders and collaborate across projects and sites. Promote scientific excellence, through external publication, presentations, and membership of conference committees and Scientific Advisory Boards This role uniquely combines cutting-edge screening expertise with deep mechanistic insight to transform early-stage target prosecution. By leveraging a range of hit identification methods (e.g. DEL, AS-MS) and rigorous mechanistic understanding, it ensures only the most viable targets progress into drug discovery, pursuing a de-risked therapeutic targeting strategy to reduce attrition and accelerate timelines. Beyond shaping the science, the successful candidate will have a real opportunity to influence and improve our ways of working, embedding best practices and innovative approaches across teams. This smarter, risk-aware strategy will ultimately deliver higher-quality medicines faster, improving outcomes and bringing life-changing therapies to patients who need them most. Furthermore, we actively encourage our colleagues to celebrate our science, by attending conferences, presenting posters, giving talks at events and publishing papers. You will form an integral part of the Cancer Research Horizon Drug Discovery team, fostering productive internal collaborations, as well as external academic and industrial partnerships, to progress novel cancer targets towards patient benefit. What are we looking for? In addition to the key strategic leadership elements of this role, the successful candidate will play a pivotal role in training and developing colleagues, including through practical contributions from the bench. You will therefore bring a genuine enthusiasm for working in the lab and guiding those around you. You will also bring: A PhD in Pharmacology, Biochemistry, Chemistry or equivalent experience, with extensive pre-clinical drug discovery experience in industry. Deep intellectual and practical knowledge of methods to assess target feasibility and druggability (eg computational modelling, protein characterisation, assay development, affinity-based methods such as DEL, AS-MS). Proven track record of innovative scientific delivery through driving impactful insight into target characterisation across a range of challenging target classes, through intellectual and laboratory-based contributions Demonstrated scientific and project leadership in highly matrixed environments, with extensive experience inspiring, developing, and guiding a diverse world class team through effective matrix management. Significant experience of establishing and leading external academic and industrial collaborations, and technology change projects, to advance organisational capability Track record of delivering results across a diverse project portfolio by leading driving strategic and scientific initiatives Strong external reputation in drug discovery, evidenced through wide personal network, external presentation and publication in high-impact journals, and influential roles on relevant external committees Strategic, credible, and future thinking leader with strong prioritisation, sound decision making under uncertainty, integrity, openness, and a commitment to EDI. Our organisation values are designed to guide all that we do. Bold: Act with ambition, courage and determination Credible: Act with rigour and professionalism Human: Act to have a positive impact on people Together: Act inclusively and collaboratively We're looking for people who can believe in and embody these organisation values and can use them to drive forward progress against our mission to beat cancer. If you're interested in applying and excited about working with us but are unsure if you have the right skills and experience we'd still love to hear from you. What will I gain? We create a working environment that supports your wellbeing and provide a generous benefits package, a wide range of career and personal development opportunities and high-quality tools. Our policies and processes enable you to improve your work-life balance, take positive steps in your career and achieve your personal wellbeing goals. You can explore our benefits by visiting our careers web page. How do I apply? We operate an anonymised shortlisting process in our commitment to equality, diversity and inclusion. CVs are required for all applications; but we won't be able to view them until we invite you for an interview. Instead, we ask you to complete the work history section of the online application form for us to be able to assess you fairly and objectively. For more information on this career opportunity please visit our website or contact us at . For more updates on our work and careers, follow us on: Linked In, Facebook, Instagram, X and YouTube.
Feb 14, 2026
Full time
Senior Principal Scientist (Project Enablement) under the leadership of Agnes Martin £58,400 - £76,000 plusbenefits (includes up to 12% pension contribution and income protection) Reports to: Associate Director, Mechanistic Pharmacology Directorate: Research & Innovation Contract: Permanent Hours: Full time 35 hours per week (4 day week would be considered) Location: Cambridge, Babraham Research Campus (minimum 3 days on site) Closing date: Open until filled. We will be shortlisting on a rolling basis and will close the vacancy once we have received sufficient applications This vacancy may close earlier if a high volume of applications is received or once a suitable candidate is found, therefore we strongly recommend that you apply early to avoid disappointment. Please let us know if there is anything or as soon as possible.in particular if there are any changes or adjustments that would make it easier for you to apply. Please contact or as soon as possible. Visa sponsorship: Cancer Research UK can consider visa sponsorship for this vacancy. If this applies to you, please ensure that this is clearly marked on your application. Recruitment process: 1st stage Teams technical and competency based itnerview, 2nd stage in person interview including pre prepared presentation At Cancer Research UK, we exist to beat cancer. We are looking for a passionate and dedicated scientific professional with extensive experience in pre-clinical drug discovery in an industrial setting. As the world's biggest medical research charity, we've helped bring eleven new cancer drugs to market. However, there is still an urgent need to bring more effective treatments to patients faster. We have developed a new approach to driving therapeutic innovation through the creation of Cancer Research Horizons (CRH). We have brought together Cancer Research UK's established drug discovery teams under one organisation and leadership team, combining our unique pipeline of cancer biology expertise and access to CRUK's world-class academic network, cutting edge technology platforms and clinical expertise to 1) bring new treatments to patients faster and 2) tackle the biggest challenges in discovering cancer drugs by seeking out more radical ideas and embracing risk in our bid to achieve success. Based at sites in Cambridge, the CRUK Scotland Institute in Glasgow, and Newcastle University, Cancer Research Horizons employs 200 staff from both industrial and academic backgrounds What will I be doing? Our strategy sets out to bring deeper mechanistic understanding at the molecular and cellular level to all stages of projects, from idea to pre-clinical candidate. In this role, you will define the vision and strategy for CRH early project enablement, establishing robust processes to select and advance promising targets into the drug discovery portfolio. You will lead and develop a matrixed team, guiding them to deliver clear go/no-go decisions through deep expertise in target feasibility and druggability. You will work closely with the Portfolio Generation team to build a sustainable pipeline, evaluating risks, shaping mitigation strategies, and ensuring projects progress efficiently toward pre-clinical development. In addition, you will provide leadership within the broader CRH TI organisation, shaping strategic direction and driving scientific and technical innovation, including championing new modalities. Key accountabilities include: Provide deep expertise in assessing target feasibility, including, but not limited to, reagent generation, mechanistic characterisation, ligandability, druggability. Work at the intersection between portfolio generation, molecular sciences, chemistry and biosciences to define and prosecute strategies that deliver clear, early go/no-go decisions across a range of challenging target classes. Provide Scientific and Strategic leadership for the assessment of novel targets and mechanisms, to drive innovation and portfolio success. Communicate effectively, to influence multiple stakeholders and collaborate across projects and sites. Promote scientific excellence, through external publication, presentations, and membership of conference committees and Scientific Advisory Boards This role uniquely combines cutting-edge screening expertise with deep mechanistic insight to transform early-stage target prosecution. By leveraging a range of hit identification methods (e.g. DEL, AS-MS) and rigorous mechanistic understanding, it ensures only the most viable targets progress into drug discovery, pursuing a de-risked therapeutic targeting strategy to reduce attrition and accelerate timelines. Beyond shaping the science, the successful candidate will have a real opportunity to influence and improve our ways of working, embedding best practices and innovative approaches across teams. This smarter, risk-aware strategy will ultimately deliver higher-quality medicines faster, improving outcomes and bringing life-changing therapies to patients who need them most. Furthermore, we actively encourage our colleagues to celebrate our science, by attending conferences, presenting posters, giving talks at events and publishing papers. You will form an integral part of the Cancer Research Horizon Drug Discovery team, fostering productive internal collaborations, as well as external academic and industrial partnerships, to progress novel cancer targets towards patient benefit. What are we looking for? In addition to the key strategic leadership elements of this role, the successful candidate will play a pivotal role in training and developing colleagues, including through practical contributions from the bench. You will therefore bring a genuine enthusiasm for working in the lab and guiding those around you. You will also bring: A PhD in Pharmacology, Biochemistry, Chemistry or equivalent experience, with extensive pre-clinical drug discovery experience in industry. Deep intellectual and practical knowledge of methods to assess target feasibility and druggability (eg computational modelling, protein characterisation, assay development, affinity-based methods such as DEL, AS-MS). Proven track record of innovative scientific delivery through driving impactful insight into target characterisation across a range of challenging target classes, through intellectual and laboratory-based contributions Demonstrated scientific and project leadership in highly matrixed environments, with extensive experience inspiring, developing, and guiding a diverse world class team through effective matrix management. Significant experience of establishing and leading external academic and industrial collaborations, and technology change projects, to advance organisational capability Track record of delivering results across a diverse project portfolio by leading driving strategic and scientific initiatives Strong external reputation in drug discovery, evidenced through wide personal network, external presentation and publication in high-impact journals, and influential roles on relevant external committees Strategic, credible, and future thinking leader with strong prioritisation, sound decision making under uncertainty, integrity, openness, and a commitment to EDI. Our organisation values are designed to guide all that we do. Bold: Act with ambition, courage and determination Credible: Act with rigour and professionalism Human: Act to have a positive impact on people Together: Act inclusively and collaboratively We're looking for people who can believe in and embody these organisation values and can use them to drive forward progress against our mission to beat cancer. If you're interested in applying and excited about working with us but are unsure if you have the right skills and experience we'd still love to hear from you. What will I gain? We create a working environment that supports your wellbeing and provide a generous benefits package, a wide range of career and personal development opportunities and high-quality tools. Our policies and processes enable you to improve your work-life balance, take positive steps in your career and achieve your personal wellbeing goals. You can explore our benefits by visiting our careers web page. How do I apply? We operate an anonymised shortlisting process in our commitment to equality, diversity and inclusion. CVs are required for all applications; but we won't be able to view them until we invite you for an interview. Instead, we ask you to complete the work history section of the online application form for us to be able to assess you fairly and objectively. For more information on this career opportunity please visit our website or contact us at . For more updates on our work and careers, follow us on: Linked In, Facebook, Instagram, X and YouTube.
Executive Assistant Salary: £42,932 - £46,306 per annum, inclusive of London allowance Full-time, permanent London, UK About us The MRC Laboratory of Medical Sciences (LMS) is a biomedical research institute where scientists and clinicians collaborate to advance the understanding of biology and its application to medicine. LMS is one of three directly funded MRC research institutes and enjoys close links with our partners at Imperial College London and at the Imperial College Healthcare NHS Trust. About the role Successful candidate will provide vital, high-level administrative support to the LMS Director and Head of Operations within a fast-paced scientific environment. This dynamic role involves proactively managing complex diaries, resolving high-level scheduling clashes independently, coordinating international travel, and acting as a key liaison for internal and external stakeholders. The role offers a high degree of variety, from drafting correspondence to acting as a delegate for administrative approvals and supporting the Senior Leadership Team. The post holder will also be expected to prepare briefing materials in advance. About You We are looking for a resourceful and reliable professional who thrives when using their initiative to solve problems in novel situations. You should possess exceptional communication skills, with a keen eye for detail and a commitment to maintaining high standards of confidentiality. The ideal candidate can balance competing priorities with tact and diplomacy. If you are a well-organised individual who prides yourself on judgment, social awareness, and ability to work independently, your skills will be highly valued in this challenging yet rewarding position. What we offer As well as the exciting opportunities this role presents, we also offer a defined benefit pension scheme and excellent holiday entitlement (30 days plus 2.5 privilege days & 8 bank holidays), family-friendly policies (6 months full pay maternity & adoption leave), a range of shopping/travel discounts, access to our Employee Assistant Programme Scheme, Health and Wellbeing Support and a salary sacrifice cycle to work scheme. Please follow this link to find out more - Benefits How to apply For full details of this post and to complete an online application, visit Executive Assistant LMS 2778 - Medical Research Council and upload your CV, names, and contacts of two references along with a cover letter stating why you are applying for this role (providing evidence against the requirements of the job as per the job description and person specification). Applications without a cover letter will not be accepted. Please quote reference number LMS 2778. Closing date: 8 March 2026 Please note that applications may be reviewed by both LMS and Imperial staff
Feb 14, 2026
Full time
Executive Assistant Salary: £42,932 - £46,306 per annum, inclusive of London allowance Full-time, permanent London, UK About us The MRC Laboratory of Medical Sciences (LMS) is a biomedical research institute where scientists and clinicians collaborate to advance the understanding of biology and its application to medicine. LMS is one of three directly funded MRC research institutes and enjoys close links with our partners at Imperial College London and at the Imperial College Healthcare NHS Trust. About the role Successful candidate will provide vital, high-level administrative support to the LMS Director and Head of Operations within a fast-paced scientific environment. This dynamic role involves proactively managing complex diaries, resolving high-level scheduling clashes independently, coordinating international travel, and acting as a key liaison for internal and external stakeholders. The role offers a high degree of variety, from drafting correspondence to acting as a delegate for administrative approvals and supporting the Senior Leadership Team. The post holder will also be expected to prepare briefing materials in advance. About You We are looking for a resourceful and reliable professional who thrives when using their initiative to solve problems in novel situations. You should possess exceptional communication skills, with a keen eye for detail and a commitment to maintaining high standards of confidentiality. The ideal candidate can balance competing priorities with tact and diplomacy. If you are a well-organised individual who prides yourself on judgment, social awareness, and ability to work independently, your skills will be highly valued in this challenging yet rewarding position. What we offer As well as the exciting opportunities this role presents, we also offer a defined benefit pension scheme and excellent holiday entitlement (30 days plus 2.5 privilege days & 8 bank holidays), family-friendly policies (6 months full pay maternity & adoption leave), a range of shopping/travel discounts, access to our Employee Assistant Programme Scheme, Health and Wellbeing Support and a salary sacrifice cycle to work scheme. Please follow this link to find out more - Benefits How to apply For full details of this post and to complete an online application, visit Executive Assistant LMS 2778 - Medical Research Council and upload your CV, names, and contacts of two references along with a cover letter stating why you are applying for this role (providing evidence against the requirements of the job as per the job description and person specification). Applications without a cover letter will not be accepted. Please quote reference number LMS 2778. Closing date: 8 March 2026 Please note that applications may be reviewed by both LMS and Imperial staff
