Associate, QC Analytical

Bristol-Myers Squibb; Leiden; On-site; EUR 42,000 - 62,000; Full time

Job summary

Bristol Myers Squibb in Leiden, Netherlands, seeks an Associate, QC Analytical to support testing of in-process, final product, and stability samples and to assist with method transfer, deviations, and continuous improvement. You will review data, ensure GMP documentation accuracy, and help train analysts in a fast-paced team.

Qualifications include a science degree, 2+ years in analytical QC, and experience with HPLC/UPLC and other analytical techniques; familiarity with LIMS/ELN is preferred.

Qualifications

• Bachelor's degree or equivalent in science.
• Netherlands: Bachelor's degree / HLO in bioanalytical science preferred.
• MLO level 4 with equivalent work experience may be considered.
• 2+ years of relevant analytical testing or QC experience in a regulated environment.
• Experience with cell-based assays, flow cytometry, HPLC/UPLC, qPCR, ELISA, and aseptic technique.
• Knowledge of regulatory and cGMP requirements.

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.

Skills

Regulatory and cGMP compliance

LIMS and ELN knowledge

Data analysis systems

Problem solving

Effective communication

Technical writing

Team collaboration

Prioritization and deadline adherence

Education

Bachelor's degree in science

MLO level 4 or equivalent

Netherlands: HLO in bioanalytical science (preferred)

Job description

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).

#LI-Hybrid

How We Work

Where you work matters – because collaboration, innovation and patient impact happen in many settings.

Our roles are structured across four work models: site-essential, site-by-design, field-based and remote‑by‑design. The model assigned to this role is based on its core responsibilities.

Learn more at https://careers.bms.com/ways‑of‑working.

Supporting People with Disabilities

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles.

Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer.

If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to [e-mail].

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BMS will consider qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

For roles based in Los Angeles County only: If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california‑residents/

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R1606160 : Associate, QC Analytical Data Privacy Link

We’re creating innovative medicines for patients fighting serious diseases. We’re also nurturing our own diverse team with inspiring work and challenging career options. No matter the role, each one of us makes a contribution. And that makes all the difference.