Senior Specialist, QC Analytical

Bristol-Myers Squibb; Leiden; Hybrid; EUR 65,000 - 85,000; Full time

Benefits offered by this job

Hybrid work model

Job summary

Bristol Myers Squibb is seeking a Senior Specialist, QC Analytical, to perform method transfer/validation and routine testing of in-process, final product, and stability samples. You will review GMP documentation, verify data, and train new analysts in a fast-paced QC environment.

The role emphasizes strong technical writing, regulatory compliance, and collaboration with cross-functional teams to ensure quality and compliance across projects.

Qualifications

• Bachelor’s degree or equivalent required, preferably in science.
• Advanced degree preferred.
• NL: Master’s or Bachelor’s degree /HLO in (bioanalytical) science required.
• 4+ years of relevant analytical testing or QC experience in a regulated environment.

Responsibilities

• Perform method transfer/validation and routine testing of samples.
• Troubleshoot and solve problems with minimal guidance.
• Data verification, data review and GMP documentation review.
• Train and mentor others on QC methods and GMP processes.

Skills

Communication

Technical writing

Analytical data systems

Education

Bachelor's degree or equivalent

Master's degree (preferred)

Tools

LIMS

Document Management

Quality Management systems

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: The Senior Specialist QC Analytical is responsible for performing method transfer/validation and routine testing including troubleshooting and problem solving. The Senior Specialist is also responsible for performing data verification and review and training new analysts. Next to that, the Senior Specialist performs documentation review and other GMP or project related activities e.g., investigations.

Key Responsibilities

• Perform method transfer/validation and routine testing of in-process, final product, and stability samples.
• Anticipate and perform troubleshooting and problem solving with minimal guidance.
• Perform data verification, data review and review of GMP documentation for general and complex methods.
• Perform QC disposition of the SOTR.
• Perform document revision, project, CAPA and deviation/ investigation related tasks and/ or continuous improvement efforts.
• Train and mentor others on QC test methods, GMP processes and procedures.
• Perform other tasks as required to support the QC laboratories.

Qualifications

• Specific Knowledge, Skills, Abilities:
• Ability to accurately and completely understand, follow, interpret and apply BMS Regulatory and cGMP requirements.
• Demonstrated technical writing skills.
• Advanced knowledge of LIMS, Document Management and Quality Management and laboratory data analysis systems preferred.
• High problem-solving ability/mentality, technically adept and logical.
• Ability to communicate effectively with peers, department management and cross-functional peers about task status, roadblocks and needs.
• 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.
• Advanced degree preferred.
• NL: Master’s or Bachelor's degree /HLO in (bioanalytical) science required.
• 4+ years of relevant analytical testing or QC experience or equivalent combination of education and experience, preferably in a regulated environment.
• Demonstrated experience in cell and molecular biology techniques (e.g. HPLC/UPLC assays, cell-based assays, flow cytometry, qPCR, ELISA, and aseptic technique).

#LI-Hybrid

We hire for skills and capabilities, not just credentials – if this role excites you, but doesn’t perfectly match your resume, we encourage you to apply anyway.

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]. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

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R1605749 : Senior Specialist, 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.