Specialist, QC Analytical

Bristol Myers Squibb · Leiden, Netherlands

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Role summary

Bristol Myers Squibb seeks a QC Analytical Specialist in Leiden to support quality control testing of in-process, final product, and stability samples. The role involves data verification, method transfer assistance, and documentation review in a regulated pharmaceutical manufacturing environment.

What they're looking for

Bachelor's degree in science or equivalent; MLO level 4 with relevant work experience considered
2+ years of analytical testing or QC experience in a regulated environment
Demonstrated proficiency with analytical techniques: HPLC/UPLC, qPCR, ELISA, flow cytometry, aseptic technique
Knowledge of LIMS, ELN, and laboratory data analysis systems preferred
Understanding of cGMP and global regulatory requirements
Strong technical problem-solving and data communication skills

What you'll be doing

Perform routine testing on in-process, final product, and stability samples
Execute testing for method transfer, validation, and verification activities
Verify analytical data and review GMP documentation for general methods
Support CAPA, deviation, investigation, and continuous improvement initiatives
Train analysts on standard laboratory procedures and duties

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Date posted6 days ago

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