GMP QC Chemist: Analytical Methods & Compliance

Eurofins PSS Insourcing Solutions; Foster City (CA); On-site; USD 60,000 - 70,000; Full time

Benefits offered by this job

Medical coverage

Dental coverage

Vision coverage

401(k) with match

Paid vacation and holidays

Job summary

Eurofins Lancaster Laboratories is seeking a GMP Chemist in Foster City, CA to support analytical testing and reference standard qualification within the Professional Scientific Services group. The role requires strong GMP knowledge, experience with UPLC/HPLC, NMR, FTIR, and empowers data handling software.

The ideal candidate has 2–5 years in an analytical GMP/GLP environment, excellent technical writing, and the ability to work independently or in a team while meeting project timelines.

Qualifications

• Experience executing small molecule analytical methods in GMP/GLP environments.
• Ability to review and verify lab data, calculations and test preparations.
• Strong writing skills for protocols, reports, and SOPs.

Responsibilities

• Support qualification and requalification of Reference Standards by analytical testing.
• Ensure GMP compliance through SOPs, training, and documentation.
• Review lab documentation and calculations before sample analysis.
• Perform data analysis and troubleshoot methods/instrumentation.
• Prepare data for presentations and technical reports.
• Coordinate shipments and testing with external labs and upload results.
• Work with cross-functional teams and external vendors to meet goals.
• Initiate investigations when needed and write transfer protocols.
• Maintain safe, organized, compliant lab environment through housekeeping.

Skills

GMP compliance

Analytical chemistry

UPLC/HPLC

NMR/FTIR

Empower software

Education

B.S. in Chemistry

M.S. in Chemistry

Tools

Empower software

Job description

Eurofins Lancaster Laboratories is seeking a GMP Chemist in Foster City, CA to support analytical testing and reference standard qualification within the Professional Scientific Services group. The role requires strong GMP knowledge, experience with UPLC/HPLC, NMR, FTIR, and empowers data handling software.

The ideal candidate has 2–5 years in an analytical GMP/GLP environment, excellent technical writing, and the ability to work independently or in a team while meeting project timelines.