Analytical Development Scientist – Cell & Gene Therapy

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

Eurofins PSS is seeking an Analytical Development Scientist to support a client focused on advancing biologics, including cutting-edge cell and gene therapies. This role plays a key part in developing and optimizing analytical assays to ensure the consistency, safety, and efficacy of novel therapies across the development pipeline.

You’ll work closely with cross-functional teams in analytical development, bioprocessing, formulation, and data science to support both manufacturing and quality control activities.

Key Responsibilities

• Design, optimize, and execute bioanalytical assays to support process development, in-process testing, and lot release.
• Perform sample analysis using platforms such as flow cytometry, ELISA, PCR (qPCR/dPCR), and cell-based assays.
• Troubleshoot assay performance and interpret complex experimental data.
• Support assay qualification, validation, and lifecycle management to ensure regulatory compliance.
• Collaborate with R&D, manufacturing, and quality teams to align analytical strategies with project goals.
• Contribute to preclinical study support by aligning assay development with experimental objectives.
• Communicate findings clearly to both technical and non-technical stakeholders.
• Support assay transfer and technical communication with CDMOs, including documentation and troubleshooting.
• Maintain lab infrastructure, including reagents, reference materials, and equipment.
• Author protocols, reports, and SOPs; stay current with emerging technologies and scientific advancements.

Qualifications

Minimum Qualifications

• Master’s degree in a relevant scientific field with 4+ years of industry experience.
• Strong expertise in qPCR and dPCR assay development.
• Proficient in multicolor flow cytometry for phenotyping and functional assays.
• Hands-on experience with mammalian cell culture, including iPSCs, tumor/cancer lines, and primary cells.
• Skilled in developing and optimizing complex bioanalytical assays.
• Strong problem-solving skills and ability to interpret complex datasets.
• Excellent written and verbal communication skills.
• Flexible and dependable; open to occasional weekend work.

Preferred Qualifications

• Ph.D. in a life science or related field.
• Specialized experience in ddPCR assay design for cell-based systems.
• Expertise in designing flow cytometry panels for functional readouts (e.g., apoptosis, proliferation).
• Experience with iPSC culture and differentiation.
• Familiarity with ICH guidelines for assay qualification and validation.
• Proficiency with digital lab tools (e.g., FlowJo, GraphPad Prism, Benchling, SharePoint, Veeva).
• Strong organizational and time-management skills in fast-paced environments.

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