QC Analytical Associate — Precise Lab Testing & Data Review

Bristol-Myers Squibb Co; Leiden; On-site; EUR 45,000 - 65,000; Full time

Job summary

Bristol Myers Squibb is seeking an Associate in QC Analytics to support in-process, final product and stability testing, with data review and verification. The role may involve method transfer, deviations, and continuous improvement tasks, and includes responsibilities such as training analysts and participating in investigations.

The position reports to QC Analytical management and requires a Bachelor’s degree (science preferred) and 2+ years of relevant experience in a regulated environment.

Qualifications

• Bachelor's degree or equivalent required, preferably in science.
• 2+ years of relevant analytical testing or QC experience in a regulated environment.
• Experience with techniques such as HPLC/UPLC, flow cytometry, qPCR, ELISA, and aseptic technique.

Responsibilities

• Perform routine testing of in-process, final product, and stability samples.
• Perform testing for method transfer/validation/verification.
• Perform data verification and GMP documentation reviews.
• Assist with document revisions, CAPA and deviation/ investigations.
• Train analysts on general job duties.
• Perform other tasks as assigned.

Skills

cGMP knowledge

LIMS/ELN

Data analysis

Technical writing

Effective communication

Education

Bachelor's degree or equivalent

MLO/HLO in bioanalytical science (NL)

Science-based degree preferred

Job description

Bristol Myers Squibb is seeking an Associate in QC Analytics to support in-process, final product and stability testing, with data review and verification. The role may involve method transfer, deviations, and continuous improvement tasks, and includes responsibilities such as training analysts and participating in investigations.

The position reports to QC Analytical management and requires a Bachelor’s degree (science preferred) and 2+ years of relevant experience in a regulated environment.