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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 laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.

The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.

In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.

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

• Work in a GLP or GMP environment with appropriate documentation and safety practices
• Develop analytical strategies in support of pharmaceutical drug products during all development phases, including supporting manufacturing process development, developing, validating and transferring analytical methods, designing stability studies to understand drug degradation mechanisms and for shelf-life assignments, and developing impurity control strategies
• Plan, direct, and review the lab work of other scientists in a matrix environment
• Collaborate with colleagues to identify appropriate analytical approaches, including use of computational predictive tools, modeling software and data visualization tools where appropriate
• Critically review and interpret scientific data to derive clear conclusions and provide direction for future work
• Communicate results and conclusions through various media including presentations and technical reports
• Evaluate new approaches and ways of working, e.g. working with outsourcing partners
• Comfortable utilizing different instrumentation and/or analytical technologies and mentoring other scientists in use and interpretation of data generated by different analytical techniques.
• Author relevant sections of the quality modules of regulatory submissions

Qualifications

• Ph.D. in Analytical Chemistry or related field, with 7-10 years of pharmaceutical R&D experience or B.S./M.S. with 10+ years of pharmaceutical R&D experience required

DESIRED QUALIFICATIONS

• Experience with mathematical modeling or coding

Additional Information

• Position is full-time, Monday-Friday, 8:00 am - 5:00 pm.
• Candidates currently living within a commutable distance of Groton, CT 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
• #LI-EB1
• Authorization to work in the United States indefinitely without restriction or sponsorship

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