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Analytical Scientist – ADTG

Eurofins

Lexington, MA, United States permanent

Posted: March 27, 2026

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Quick Summary

We are seeking an experienced analytical scientist to join our team in Lexington, MA, and contribute to the development of life sciences testing services.

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!

The Analytical Scientist – ADTG will contribute as part of a team supporting analytical development, characterization, and release testing of biological therapeutics in a regulated environment. This role has a strong emphasis on Size Exclusion Chromatography (SEC) for protein purity, aggregation, and stability assessments.

Key responsibilities include:

• Independently perform routine analytical testing with a primary focus on Size Exclusion Chromatography (SEC) using HPLC/UPLC platforms to support biologics release and characterization.
• Execute additional chromatographic and electrophoretic techniques as needed, including CEX, RP-HPLC, CE-SDS (Maurice and PA800), icIEF (Maurice), iCE, P20, and P80, using established test methods.
• Analyze, interpret, and document SEC data to assess molecular weight distribution, aggregation, and degradation of protein therapeutics.
• Prepare and review protocols, reports, data summaries, and presentations in accordance with established procedures.
• Demonstrate hands-on troubleshooting capabilities for SEC methods, including column performance, system suitability, and method variability.
• Conduct all laboratory activities in compliance with cGMP/GLP, safety standards, and regulatory requirements.
• Apply independent judgment in technique selection, method execution, data analysis, and problem solving for work of moderate scope and complexity.
• Support non-laboratory tasks when assigned, including documentation updates, method transfers, and process improvement initiatives.

Required:

• Bachelor’s degree in Analytical Chemistry, Biochemistry, Cell and Molecular Biology, Pharmaceutical Sciences, or a related scientific discipline with 2+ years of hands-on experience performing Size Exclusion Chromatography (SEC) using HPLC or UPLC systems.
• OR Master’s degree in a related scientific discipline with 6+ months of directly relevant internship or hands-on experience specifically involving SEC.
• Strong working knowledge of SEC theory, method execution, and data interpretation for biologics and protein-based products.
• Proficiency with HPLC/UPLC instrumentation, including basic method troubleshooting.
• Familiarity with cGMP/GLP environments, data integrity principles, and regulated documentation practices.
• Ability to learn new techniques, manage multiple tasks, maintain accurate records, and follow detailed procedures.
• Authorization to work in the United States indefinitely without restriction or sponsorship.

Preferred:

• Experience supporting biologic therapeutics in analytical development or QC environments.
• Exposure to complementary techniques such as CEX, CE-SDS, or icIEF.
• Prior work in CRO, CDMO, or client-facing laboratory settings.

The position is full-time, first shift, Monday-Friday with overtime as needed. Candidates living within a commutable distance of Lexington, MA are 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
• Compensation: $31.00-$34.00 per hour based on education and experience

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

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