Jobid: 627320747060895993 (0.0502)
At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it.
Position Summary
Responsible for supporting QC testing for in-process, final product, and stability samples, including data review/verification. May assist with method transfer, documentation, deviations, investigations, and continuous improvement efforts.
Duties/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.
Reporting Relationship
This position will report to QC Analytical management.
Qualifications
Specific Knowledge, Skills, Abilities:
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.
Education/Experience/ Licenses/Certifications:
Bachelor’s degree or equivalent required, preferably in science. Netherlands: Bachelor’s degree / HLO in (bioanalytical) science preferred. MLO level 4 with equivalent combination of work experience may be considered.
2+ years of relevant analytical testing or QC experience or equivalent combination of education and experience, preferably in a regulated environment.
Demonstrated experience in various techniques (e.g., cell-based assays, flow cytometry, HPLC/UPLC, qPCR, ELISA, and aseptic technique).
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