Analytical Chemist I — GMP Testing & Method Validation

Eurofins USA BioPharma Services; Lancaster (Lancaster County); On-site; USD 60,000 - 90,000; Full time

Benefits offered by this job

Medical/Dental/Vision

Life and Disability Insurance

401(k) with company match

Paid vacation and holidays

Job summary

Eurofins USA BioPharma Services in Lancaster, PA is seeking a chemist with GMP experience to perform a range of analytical tests and validation activities. The role involves method transfers, compliance documentation, and client-site support as needed.

The ideal candidate will have a chemistry-related bachelor's degree, 2 years of pharmaceutical experience, and strong HPLC/validation skills, with eligibility to work in the U.S. without sponsorship.

Qualifications

• Bachelor's degree in chemistry, analytical chemistry, biochemistry, or related field.
• 2 years of pharmaceutical experience in a cGMP environment.
• HPLC and validation experience.
• Authorization to work in the United States indefinitely without restriction or sponsorship.

Responsibilities

• Perform various type of testing using chromatographic systems, Karl Fischer, UV/Spec, HPLC, IC, IR, ICP, AA, TGP, DSC, PDA, titrators, TLC, and dissolution apparatus.
• Execute specialized analyses and 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.
• Develop and execute validation plans.
• Carry out method transfers and feasibility studies.
• Train technical staff.
• Some travel to client sites for technical meetings could be required.

Skills

HPLC

Validation

Protein chromatography

GMP

Education

Bachelor's degree in chemistry/analytical chemistry/biochemistry

Job description

Eurofins USA BioPharma Services in Lancaster, PA is seeking a chemist with GMP experience to perform a range of analytical tests and validation activities. The role involves method transfers, compliance documentation, and client-site support as needed.

The ideal candidate will have a chemistry-related bachelor's degree, 2 years of pharmaceutical experience, and strong HPLC/validation skills, with eligibility to work in the U.S. without sponsorship.