Senior Chemist

Eurofins BioPharma Product Testing North America; Lancaster (Lancaster County); On-site; USD 70,000 - 90,000; Full time

Benefits offered by this job

Comprehensive medical, dental, and vision coverage

401(k) with company match

Paid vacation and holidays

Job summary

A leading bio-pharmaceutical testing firm in Lancaster is seeking a Senior Analytical Chemist specializing in method development and validation. You will perform a variety of tests using advanced chromatographic systems and play a vital role in documenting work for GMP compliance. Ideal candidates have 4–8 years of relevant experience, hold a degree in chemistry, and can work in a fast-paced environment. This full-time position offers comprehensive benefits and competitive compensation.

Qualifications

• 4–8 years of experience in the analytical chemistry industry.
• Three years of pharmaceutical experience in a cGMP environment.
• Authorization to work in the US without restriction.

Responsibilities

• Perform various testing using chromatographic systems.
• Develop and execute validation plans.
• Train technical staff.

Skills

Chromatographic systems

Method validation

Troubleshooting

EMPOWER

HPLC

Education

Bachelor's or Master's degree in chemistry or related field

Tools

Karl Fischer

UV/Spec

ICP

Job description

Job Description

Senior Analytical Chemist – Method Development & Validation

Responsibilities

• Perform various types of testing using chromatographic systems, Karl Fischer (Coulometric and Volumetric), UV/Spec, wet chemistry analyses, HPLC, IC, IR, ICP, AA, TGP, DSC, PDA, auto-titrators, TLC, and dissolution apparatus.
• Execute specialized analyses, method transfer, and feasibility testing.
• Document work as required for GMP compliance.
• Perform tests accurately.
• Troubleshoot method and instrumentation problems.
• Use office and instrumentation-specific computer software.
• Produce written reports (e.g., SOP, OMC, client reports).
• Develop and execute validation plans.
• Carry out method transfers and feasibility studies.
• Train technical staff.
• Travel to client sites for technical meetings as required.

Ideal Candidate

• 4–8 years of experience within the industry.
• Experience using EMPOWER and HPLC.
• Experience with validation.

Minimum Qualifications

• Bachelor's or Master's degree in chemistry or related field, or equivalent experience.
• Three years related pharmaceutical experience in a cGMP environment.
• Authorization to work in the United States indefinitely without restriction or sponsorship.

Working Schedule

Full‑time, First Shift, Monday‑Friday 8 am–4 pm. Candidates currently living within a commutable distance of Lancaster, PA are encouraged to apply. 25% travel may be required. Remote work is not offered.

Benefits

• Comprehensive medical, dental, and vision coverage.
• Life and disability insurance.
• 401(k) with company match.
• Paid vacation and holidays.

EEO Statement

Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.