QC Analytical Specialist: Data-Driven Lab Impact

Bristol Myers Squibb; Leiden; On-site; EUR 60,000 - 85,000; Full time

Job summary

Bristol Myers Squibb is seeking a Specialist, QC Analytical to support in-process, final product, and stability testing. You will review data, participate in method transfers, deviations, and investigations while contributing to continuous improvement and proper GMP documentation, reporting to QC Analytical management.

The role requires a strong foundation in analytical techniques, regulatory understanding, and effective communication within a fast-paced team.

Qualifications

• Bachelor's degree in science or equivalent required.
• 2+ years in analytical testing or QC in regulated environment.
• Experience with techniques (cell-based assays, flow cytometry, HPLC/UPLC, qPCR, ELISA).

Responsibilities

• Perform routine QC testing for in-process, final product, and stability samples.
• Perform data verification and GMP documentation review for methods.
• Assist with method transfer, deviations, investigations, and continuous improvement.
• Train analysts on general duties.
• Support project tasks and CAPA/ investigations as needed.

Skills

cGMP knowledge

Analytical testing

Data review & verification

Written documentation

Teamwork & communication

Problem solving

Education

Bachelor's degree in science

MLO level 4 / equivalent experience

Tools

LIMS

ELN

HPLC/UPLC

Job description

Bristol Myers Squibb is seeking a Specialist, QC Analytical to support in-process, final product, and stability testing. You will review data, participate in method transfers, deviations, and investigations while contributing to continuous improvement and proper GMP documentation, reporting to QC Analytical management.

The role requires a strong foundation in analytical techniques, regulatory understanding, and effective communication within a fast-paced team.