Company Description
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 our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.
In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 47,000 staff across a network of more than 900 independent companies in over 50 countries and operating more than 800 laboratories. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing.
In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years.
Job Description
The position will support a client team that is responsible for ensuring the consistency, safety, and efficacy of biologics, including cutting-edge cell and gene therapies. The successful candidate will work in close partnership with analytical development, bioprocessing, formulation, and data science groups to support manufacturing and quality control activities across the client’s development pipeline.
We are seeking a skilled analytical development scientist who will contribute to the development of the client’s islet cell therapy platform. This role will involve designing, optimizing, and executing bioanalytical assays for use in process development, in-process testing, and lot release. Knowledge and expertise in mammalian cell culture, flow cytometry, and molecular assays, including PCR, are a must. The successful candidate must be self-motivated and able to work independently to troubleshoot and interpret experimental results and effectively present conclusions.
Job Responsibilities and Requirements
- Develop, optimize, and execute a range of analytical assays to support product development and batch release.
- Perform sample analysis using a broad set of platforms such as flow cytometry, ELISA, PCR, and cell-based assays.
- Investigate and resolve assay-related challenges by applying scientific and technical problem-solving skills.
- Support assay qualification, validation, and lifecycle management to ensure reliability and regulatory compliance.
- Collaborate with cross-functional teams, including R&D, manufacturing, and quality to ensure alignment on analytical goals and timelines.
- Contribute to preclinical study support by aligning analytical strategies with experimental objectives.
- Interpret experimental data, summarize results clearly, and communicate findings to technical and non-technical audiences.
- Support assay transfer and technical communication with CDMOs, including troubleshooting, documentation review, and knowledge transfer.
- Maintain laboratory infrastructure, including oversight of reagents, reference materials, and analytical equipment.
- Author technical documentation such as protocols, reports, and standard operating procedures.
- Continuously evaluate emerging technologies and scientific approaches to improve assay performance and robustness.
Qualifications
Educational Requirements:
- B.S. with 4-6 years of experience in bioassay or analytical development OR
- M.S. and 2-3 years of experience in bioassay or analytical development OR
- Ph.D. in life sciences or a related field, with 0-1 year of industry experience in bioassay or analytical development
Minimum Qualifications:
- Hands-on Experience with Flow cytometry and molecular assays such as PCR.
- Proficiency in mammalian cell culture techniques.
- Ability to troubleshoot and interpret experimental results and effectively present conclusions.
Preferred Qualifications:
- Familiarity with data analysis and visualization tools (e.g., GraphPad Prism, FlowJo) and digital lab platforms (e.g., Benchling, SharePoint, Veeva).
- Working knowledge of iPSC differentiation is preferred, and hands-on experience with iPSC cells is a plus.
- Experience in troubleshooting analytical methods and implementing improvements.
- Understanding of regulatory standards and ICH guidelines applicable to assay development.
- Strong time-management and organizational skills, with the ability to handle multiple priorities under tight deadlines.
- Excellent communication skills and the ability to collaborate in a team-oriented, cross-functional environment.
- Willingness to take on additional responsibilities as needed, including occasional weekend work.
Additional Information
What to Expect in the Hiring Process:
- 10-15 Minute Phone Interview with Region Recruiter
- 45-60 Minute Virtual Interview with Manager and/or Group Leader
- 45-60 Minute In-Person Meeting over Coffee for a Casual Discussion of the Role
ThePosition is Full Time, Monday-Friday, 8am-5pm. Candidates currently living within a commutable distance of Boston, MA are encouraged to apply.
- Excellent full-time benefits including comprehensive medical coverage, dental, and vision options
- Life and disability insurance
- 401(k) with company match
- Paid vacation and holidays
Eurofins Lancaster Laboratories Professional Scientific Services® (PSS) is a global, award-winning insourcing solution that places our people at our clients’ sites, dedicated to running and managing laboratory services while eliminating headcount, co-employment, and project-management worries.
We infuse our 55-year track record of scientific and laboratory operations expertise, as well as HR and great place to work best practices, to recruit, hire, train, and manage highly qualified scientists to perform laboratory services using our client’s quality systems and equipment.
To learn more about Eurofins Lancaster Laboratories, please explore our website www.eurofinsus.com.
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.
