QC Analyst: Analytical Methods & Data Review

Bristol Myers Squibb EU Policy

Leiden

On-site

EUR 45,000 - 60,000

Full time

2 days ago

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Job summary

Bristol Myers Squibb is seeking a QC Analytical Associate to support testing of in-process, final product and stability samples, with data review and method transfer support. The role involves data verification and adherence to GMP documentation, with opportunities to participate in deviations, investigations, and continuous improvement.

The successful candidate will work within a fast-paced team, ensuring accurate technical documentation and training junior staff as required.

Qualifications

Bachelor’s degree or equivalent in science.
2+ years of analytical testing or QC experience in a regulated environment is preferred.
Experience with cell-based assays, flow cytometry, HPLC/UPLC, qPCR, ELISA and aseptic technique is desirable.

Responsibilities

Perform routine testing of in-process, final product, and stability samples.
Perform testing for method transfer/validation/verification.
Review GMP documentation and data verification consistently.
Possibly participate in deviations, investigations, CAPA and continuous improvement tasks.
Train analysts on general job duties and procedures.