HireFT
Browse JobsHow it worksPricingAboutSuccess Stories
    Back to jobs
    BR

    Bristol Myers Squibb

    Biopharmaceutical

    Senior Specialist, QC Analytical

    Leiden, NetherlandsFull-time4+ yrs experiencePosted 4w ago
    All Bristol Myers Squibb jobs

    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 [email protected]. 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.

    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/

    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 [email protected] 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.

    R1605749 : Senior Specialist, QC Analytical

    Job details are sourced from the employer's original posting.

    Open job posting
    BR

    About the company

    Bristol Myers Squibb

    Bristol Myers Squibb is a biopharmaceutical company focused on discovering, developing, manufacturing, and marketing innovative medicines.

    View all Bristol Myers Squibb jobs
    Industry
    Biopharmaceutical
    Open roles
    137

    Interested in this role?

    Apply with HireFT

    Free to start — no card required.

    Your fit

    How well do you match?

    Sign in to see how your résumé lines up with this role.