Are you looking for an exciting opportunity, a rewarding, enriching, and fulfilling career, and the opportunity to grow to greater levels of success with a company that values you? Then look no further! Join Eurofins PSS: a world class company that is growing by leaps and bounds while making a difference to humanity.

At Eurofins PSS, you will gain experience working in state-of-the-art laboratories, and be a part of a team that is dedicated to testing, development, and advancement of life-saving drug products to make the world a healthier and happier place to live in. Our people are our chemistry and we need talented people like you now more than ever.

Eurofins PSS is an international life sciences company, providing a unique range of analytical testing services to clients making life and our environment safer, healthier and more sustainable. Eurofins PSS works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate.

Why Eurofins?

• A focus on your professional development because your growth is our growth

• A chance to step in to the pharmaceutical/biopharmaceutical industry and move up the ladder of success to help you achieve your career goals

• Healthy work/life balance, an essential need for employee satisfaction

• Excellent benefits such as tuition reimbursement, mentoring and leadership programs, 401k, medical/vision/dental insurance, PTO, and much more!

• Opportunity for involvement in several innovative committees surrounding sustainability, equality, development, and much more!

• 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 

Base Compensation ranges from $21-28/hour dependent on relevant experience and education. Position is full-time, working Tuesday - Saturday, 1st shift 8:00 AM- 4:00 PM

• Candidates currently living within a commutable distance of Rensselaer, NY 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

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