Research Associate - Translational Toxicology (Cellular Assays)

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.

Eurofins PSS is seeking a Research Associate, Translational Toxicology (Cellular Assays) to support in vitro safety and de‑risking strategies for novel therapeutic candidates. This role is highly hands‑on and centers on the design, execution, and interpretation of cellular assays, with a strong emphasis on flow cytometry–based immunophenotyping and multiplexed ELISA platforms.

The Research Associate will be embedded on a client site and work cross‑functionally with toxicology, DMPK, chemistry, and discovery biology teams to support translational safety decision‑making throughout the drug discovery and early development process. The role is scheduled to start in July 2026.

Key Responsibilities

• Design, execute, and interpret in vitro translational toxicology experiments, including:
  • Flow cytometry–based cellular immunophenotyping
  • Multiplexed and quantitative ELISA assays (e.g., MSD, Luminex)
• Culture and maintain complex cellular models to support safety screening and proof‑of‑mechanism studies
• Contribute to the development and optimization of cellular and immunoassay‑based safety assays
• Collaborate closely with discovery toxicologists, medicinal chemists, and research scientists to help prioritize and de‑risk drug candidates
• Perform routine data analysis, troubleshooting, and interpretation of experimental results
• Maintain accurate and compliant documentation, including electronic databases and laboratory notebooks
• Stay current on relevant scientific literature and emerging assay technologies
• Present experimental findings at internal group and departmental meetings

Required Knowledge & Skills

• Strong foundation in cell and molecular biology
• Demonstrated hands‑on experience planning, executing, and interpreting in vitro cellular assays
• Proficiency with mammalian cell culture and sterile technique
• Excellent attention to detail, organization, and ability to work independently in a fast‑paced environment

Preferred Experience

• Flow Cytometry for cellular immunophenotyping and safety assessment
• Immunoassays, including multiplexed or quantitative ELISA platforms (MSD, Luminex preferred)
• Experience with high‑throughput cell culture formats and liquid handling systems
• Basic data processing and statistical analysis skills

Education & Experience

• Master’s degree in Cell Biology, Molecular Biology, or a related discipline with 0–1 years of relevant experience, or
• Bachelor’s degree in a related discipline with 1–2 years of relevant experienc

Authorization to work in the United States indefinitely without restriction or sponsorship.

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
• 60 Minute Onsite Meeting with the Team

Additional Details:

This is a full‑time, onsite role operating on a first‑shift schedule (Monday through Friday, 8:00 AM to 5:00 PM). Overtime is required as needed, with occasional weekend work. Candidates located within a commutable distance to Boston, MA, are strongly encouraged to apply.

Excellent full-time benefits include:

• comprehensive medical coverage, dental, and vision options
• Life and disability insurance
• 401(k) with company match
• Paid vacation and holidays
• Hourly rate is between $31 - $34, depending on education and experience

Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.