Specialist, QC Analytical

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

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).

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.

Candidate Rights

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

Data Protection

We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https //careers.bms.com/fraud-protection.

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

If this posting is missing required information required by local law or incorrect, contact BMS at [e-mail] with the Job Title and Requisition number. Do not send application-related inquiries to this email. To check your application status, please login to your Candidate Home Account.

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/

R1606089 Specialist, QC Analytical