Toxicology Research Associate

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 who will be responsible for designing human and preclinical animal in vitro models to support prioritization and de-risking of novel therapeutic agents throughout the drug discovery and development process. This candidate will work directly on a client site with stakeholders from several functional areas, including toxicology, chemistry, DMPK, and research. The role is scheduled to start in July 2026. 

Key Responsibilities:

• Designs, executes, and interprets in vitro safety experiments such as flow cytometry and multiplexed ELISA assays with a high degree of reliability
• Culture of complex cellular models for drug screening and proof of mechanism studies
• Contribute to the development and implementation of in vitro safety assays to support the selection and de-risking of potential drug candidates through close interactions with discovery toxicologists, medicinal chemists, and research functions
• Conducts own experimental troubleshooting on routine problems
• Maintains accurate and reliable record keeping, including database management, notebooks, and all other pertinent documentation.
• Keeps up to date with current literature in the area of expertise and participates in relevant continuing education activities
• Present studies effectively at internal group/department research meetings

Knowledge and Skills:

• Demonstrates technical proficiency and skill in planning, executing, and interpreting in vitro experiments
• Knowledge of cell and molecular biology and basic cell culture/sterile technique
• Preferred experience in development and/or execution of immunoassays including multiplexed ELISA assays (e.g., MSD or Luminex) and cellular immunophenotyping by Flow Cytometry
• Preferred experience using liquid handling instruments and high-throughput cell culture formats
• Basic data processing and statistical skills
• Excellent multi-tasking skills, attention to detail and ability to work independently

Education and Experience:

• Masters Degree (or equivalent degree) in Cell Biology, Molecular Biology or related science and 0-1 years of relevant employment experience, or
• Bachelors Degree (or equivalent degree) in Cell Biology, Molecular Biology or related science and 1-2 years of relevant employment experience

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.