Senior Specialist, QC Analytical, Cell Therapy A2 Shift

Senior Specialist, QC Analytical, Cell Therapy A2 Shift Position Summary Responsible for supporting QC testing for in-process, final product, and stability samples, including data review and verification. Perform method troubleshooting, training, and transfer/validation. Execute document revisions, projects, deviations/investigations/CAPA, and continuous improvement efforts. Shift A2: Sunday – Wednesday, 2 PM – 12 AM Key Responsibilities Perform method transfer/validation and routine testing of in-process, final product, and stability samples. Anticipate and perform routine troubleshooting and problem solving with minimal guidance. Perform data verification, data review, and review of GMP documentation for general and complex methods. Perform document revision, project, CAPA, and deviation/investigation related tasks and/or continuous improvement efforts. Train and mentor others on QC test methods, processes, and procedures. Perform other tasks as assigned. Qualifications & Experience Specific Knowledge, Skills and Abilities Ability to accurately and completely understand, follow, interpret and apply global regulatory and cGMP requirements. Demonstrated technical writing skills. High problem‑solving ability, 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. Advanced knowledge of LIMS, ELN and laboratory data analysis systems preferred. Education / Experience / Licenses / Certifications Bachelor’s degree or equivalent required, preferably in science. (Netherlands: 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., cell‑based assays, flow cytometry, qPCR, ELISA, and aseptic technique). Compensation Overview Devens – MA – US: $43.84 – $53.12 per hour (full‑time employee basis). Additional incentive cash and stock opportunities may be available. Final compensation is determined based on demonstrated experience. Benefits eligibility may vary by job and location. For more on benefits, visit career site . Benefits Health Coverage: Medical, pharmacy, dental, and vision care. Well‑being Support: Programs such as BMS Well‑Being Account, BMS Living Life Better and Employee Assistance Programs. Financial Well‑being and Protection: 401(k) plan, short‑ and long‑term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support and survivor support. Paid Time Off: Flexible time off (unlimited with manager approval), 11 paid national holidays, optional holidays (varies by location), unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for various needs and an annual Global Shutdown between Christmas and New Years Day. EEO, Candidate Rights and Data Protection Supporting People With Disabilities: Contact for accommodations. Candidate Rights: BMS will consider qualified applicants with arrest and conviction records, pursuant to applicable laws. Data Protection: We will never request payments, financial information, or social security numbers during our application or recruitment process. Legal Statements Visit Equal Employment Opportunity statement and fraud protection information . #J-18808-Ljbffr Bristol Myers Squibb