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 is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins 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. The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.

In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 50 countries. 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.

In 2020, Eurofins generated total revenues of EUR € 5.4 billion, and has been among the best performing stocks in Europe over the past 20 years.

• Support the Manufacturing, Process Sciences (PS) and Quality Control (QC) departments through the troubleshooting, validation, transfer and application of analytical test procedures, and clinical product testing as needed
• Perform routine stability and release chemistry and biochemistry testing for pre-clinical and early clinical phase programs including techniques such as capillary electrophoresis (CE), ELISA, MCE, and iCIEF
• Perform assay qualification/validation experiments.
• Transfer new or improved control test procedures to customer groups.
• Troubleshoot established test methods used in development and release testing. Provide analytical support in troubleshooting process and formulation problems.
• Assist in the analysis of samples generated from lab scale process studies.
• Assist in product failure or customer complaint investigations
• Assist QC Release group with overflow routine testing
• Tabulate and report results quickly and accurately
• Present findings at group and possibly at interdepartmental meetings.
• Maintain lab supplies and equipment for GMP compliance.
• Produce and maintain accurate records.
• Train lower-level group members.

• Bachelor’s degree in chemistry, biology, or other science related degree concentration, or equivalent directly-related experience
• Experience in a cGMP pharmaceutical environment
• Strong computer, scientific, and organizational skills
• Excellent communication (oral and written) and attention to detail
• Ability to work independently and as part of a team, self-motivated, adaptability, and a positive attitude
• Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies
• Authorization to work in the United States indefinitely without restriction or sponsorship

Position is full-time, 1st shift, Tuesday-Saturday or Monday-Friday. Candidates currently living within a commutable distance of Rensselaer, NY and the surrounding areas 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 is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.

Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.