Analytical QC Specialist — Data-Driven Methods & Validation

Bristol-Myers Squibb Co

Leiden

Hybrid

EUR 55,000 - 75,000

Full time

10 days ago

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Benefits offered by this job

Health insurance

Job summary

Bristol Myers Squibb in the Netherlands is seeking a QC Analytical Specialist to support in-process, final product, and stability testing, including data verification and GMP documentation. You will assist with method transfer/validation, deviations, investigations, and continuous improvement, training analysts, and ensuring adherence to global regulatory requirements.

The role requires a bachelor’s degree in science, 2+ years in analytical QC, knowledge of HPLC/UPLC, flow cytometry and other

Qualifications

Ability to accurately and completely understand, follow, interpret and apply Global Regulatory and cGMP requirements.
Knowledge of LIMS, ELN and laboratory data analysis systems preferred.
Problem-solving ability/mentality, technically adept and logical.
Ability to communicate effectively with peers, department management and cross-functional peers.
Experience with writing technical documents preferred.
Ability to work in a fast-paced team environment, meet deadlines, and prioritize work.

Responsibilities

Perform routine testing of in-process, final product, and stability samples.
Perform testing for method transfer/validation/verification.
Perform data verification, data review and review of GMP documentation for general methods.
May perform document revision, project, CAPA and deviation/ investigation related tasks and/ or continuous improvement efforts.
Train analysts on general job duties.
Perform other tasks as assigned.