Eurofins
Analytical Scientist
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About Eurofins
Eurofins is an international network of independent life sciences companies, providing a unique range of analytical testing services to clients across multiple industries. We ensure the safety, health, and sustainability of products—from the food you eat, to the water you drink, to the medicines you rely on. Our labs help the world’s biggest companies verify product authenticity, accuracy of labeling, and high standards of safety.
Eurofins PSS Insourcing Solutions® is a global, award-winning approach that places our skilled team directly at client sites. We manage operations seamlessly, ensuring strategic long-term commitments while leveraging our customer’s facilities, equipment, and methodologies—all while maintaining Eurofins’ cGMP compliance.
We’re proud to be an armed forces-friendly employer, welcoming applications from reservists, veterans (incl. wounded/sick), cadet instructors, and military spouses/partners.
If you want to contribute to making the world safer and healthier, join the extraordinary Eurofins network.
Job Title: Analytical Scientist (Eurofins-Managed PSS)
Location: Bristol Myers Squibb Moreton facility (Wirral) Employment Type: Permanent, full-time Hours: 35hours/week (flexible, 7am–7pm on 5/7 days as needed)
Key Details:
- Permanent staffing by Eurofins PSS (role not employment with Bristol Myers Squibb).
- Visa sponsorship unavailable.
- On-site support at a pharmaceutical client site, with full responsibility for supplying testing services.
About the Role
As an Analytical Scientist, you will perform essential testing for pharmaceutical products to ensure optimal quality, safety, and regulatory compliance. Your work will directly enhance drug efficacy and public trust in medicines by delivering accurate, timely, and transparent results.
This role requires technical expertise, diligence, and ability to adapt to evolving industry standards. Your contributions will impact product reliability and client satisfaction.
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Responsibilities
You will be responsible for the following core tasks:
- Performing routine & non-routine analysis:
- Execute tests for finished pharmaceutical products, primarily using HPLC, dissolution testing, and Karl Fischer moisture determination.
- Supporting technology transfers:
- Aid in implementing new product methods, aligning with client procedures.
- Assisting in analytical development & validation:
- Participate in method development and validation tasks as needed.
- Ensuring GMP compliance:
- Review analytical data for Good Manufacturing Practice (GMP) adherence.
- Investigate Out of Specification (OOS) results and action limits when required.
- Documentation & reporting:
- Log data in system (echo market Electronic Laboratory Notebooks, LIMS) per client policies.
- Prepare/approve test results for final submission.
- Productivity & operational excellence:
- Maintain agreed output metrics (e.g., test numbers, cycle times).
- Support laboratory audits and method revisions.
- Test quality control (QC) samples per internal/external requirements.
- Client-facing interaction:
- Liaise with client representatives for updates and continuous improvement.
- Collaborate with stakeholders to optimize processes efficiently.
Requirements
Essential Criteria:
- Degree in Chemistry or related life sciences discipline; relevant industrial experience may substitute formal qualifications where evidence of skills exists.
- Sound foundational analytics knowledge, sufficient understanding of chromatographic principles.
- Practical experience in HPLC, dissolution, Karl Fischer, and UV spectrophotomtery (solid dose preferred).
- Comprehension of GMP frameworks, including behaviours like:
- Potential Cause explanations for deviations.
- Troubleshooting improved analytical/instrument issues.
- Accurate documentation compliance.
- Proficiency in electronic lab notebooks (ELNs), Laboratory Information Management Systems (LIMS), and MS Office.
- Flexible mindset: ability to reprioritize tasks, assist cross-functionally, and participate in continuous improvement initiatives.
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Desirable Attributes:
- Previous experience at a pharmaceutical GMP lab.
- Strong time-management skills and willingness to learn.
- Customer service orientation: focused on achieving/cl.and exceeding expectations.
Benefits & Perks
As a valued member of Eurofins, you’ll enjoy:
✔ Annual recognition plans highlighting employee achievements. ✔ Progressive holiday entitlement based on length of service. ✔ Health Cash Plan (for routine care, optical health, dental). ✔ Life Assurance cover accessible from day one (4x annual salary). ✔ Pension Plan (automatic eligibility after 3 months). ✔ Employee Assistance Programme (EAP), supporting personal/work challenges with 24/7 confidential support. ✔ Volunteering days to support local community causes. ✔ On-site parking for convenient, eco-friendly commutes. ✔ Global mobility opportunities to experience different Eurofins labs worldwide. ✔ Perkbox discounts across products/services, including reimbursement on travel, groceries, media, and more.
Commitment to Diversity & Equal Opportunity
Eurofins is an Equal Opportunity Employer. We promote diversity in race, creed, disability status, religious affiliation, national origin, age, gender identity, veteran status, or any other characteristic that contributes to a global workforce.
Next Steps
Eurofins values fostering meaningful engagement with our team. If selected, you’ll undergo an assessment centre or staged interview process to showcase your expertise.
We collect and process candidates’ data as part of standard recruitment practices, prioritizing transparency and confidentiality.
Note: Bristol Myers Squibb does not manage recruitment or employment details for this position.
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