Job Description

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.

Qualifications

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.

Additional Information

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.