Job Description

The work we do at Eurofins Professional Scientific Services matters, and so do our employees. At Eurofins PSS, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package.

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.

If you’re looking for a rewarding career, a place to call home, apply with us today!

We are seeking a motivated Scientist to join our In‑Process Analytics team. This role supports biological therapeutic product release and characterization testing within a regulated, compliance‑driven environment. The Scientist will perform routine analytical testing, execute established methods, and support high‑throughput workflows as part of a small, collaborative team.

This position is hands‑on and testing‑focused, with full responsibility for method execution, documentation, data analysis, and routine troubleshooting.

Key Responsibilities

• Execute established analytical methods to support characterization and release testing of biological therapeutics
• Perform 100% testing and method execution, including associated documentation and routine troubleshooting
• Conduct routine testing using:
  • Simple LC‑based assays
  • Plate‑based assays for protein characterization and impurity quantitation
• Support high‑throughput testing using fully automated liquid handling systems
• Analyze data, document results, and ensure accuracy and completeness of records
• Apply advanced scientific principles, theories, and concepts related to product development
• Conduct all work in compliance with cGMP/GLP, safety, and regulatory requirements
• Exercise independent judgment in:
  • Technique and method selection
  • Protocol execution
  • Data analysis and interpretation
• Collaborate effectively within a small team to meet testing and project objectives

Qualifications

Required Qualifications

• Bachelor’s degree in Cell & Molecular Biology, Biochemistry, Pharmaceutical Sciences, or a related biological/analytical discipline with 0–2 years of relevant industry experience (biotechnology, pharmaceutical, or related).
• Foundational understanding of scientific principles with exposure to plate‑based and/or LC‑based analytical techniques
• Strong computer skills, including Microsoft Excel and Word
• Excellent written and verbal communication, attention to detail, and organizational skills.
• Ability to work independently and within a team, demonstrating adaptability, self‑motivation, and a positive attitude.
• Ability to learn new techniques, multitask, maintain accurate records, follow instructions, and comply with company policies.
• Authorization to work in the United States indefinitely without sponsorship

Preferred Qualifications

• Hands‑on experience with one or more of the following:
  • Plate‑based methods ELISA, CE‑SDS, DNA PCR
  • LC‑based methods RP, IEX, SEC, ICE, iCiEF
• Experience operating laboratory instrumentation such as plate washers/readers, HPLC, and UPLC
• Familiarity with laboratory and data systems including Empower, SoftMax Pro, and Excel
• Basic understanding of industry practices, documentation standards, and regulated laboratory environments

Additional Information

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
• 30 Minute In-Person Onsite Meeting with the Team

The position is Full Time, Monday-Friday, 8am-5pm. Candidates currently living within a commutable distance of Lexington, MA, are encouraged to apply.

What We Offer:

• 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
• Yearly goal-based bonus & eligibility for merit-based increases
• Hourly rate is between $24-38 per hour, depending on education and experience

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