Technician 2, QC Sample Management, A1 shift, Cell Therapy

Job Summary Associate for QC Sample Management at the Cell Therapy Facility (CTF) in Devens, MA. This role is responsible for the movement and control of QC samples and materials, including in‑process, finished drug product, characterization, retain, and stability samples processed through the QC laboratories. Work Hours 12‑hour rotating shift (36/48 hours over a 2‑week period). Shifts run from 6:00AM to 6:00PM and include working every other weekend and holidays that fall on scheduled workdays. Flexibility to work irregular hours and short‑notice overtime may be required. Responsibilities Handle test samples throughout the sample lifecycle: receipt, storage, distribution, transfer, and disposal. Facilitate cold‑chain transfers of samples. Ensure samples and materials are appropriately labelled and maintain sample tracking, labelling, and chain‑of‑custody records in accordance with regulatory requirements and written procedures. Maintain inventory and distribution of QC samples and materials to functional groups as scheduled or requested. Apply 5S and FIFO principles as appropriate. Support performance metrics for the sample management group. Support investigations through data gathering or interview processes. Collaborate with other departments to identify and implement process efficiencies. Communicate effectively with management regarding task completion, roadblocks, and needs. Perform other tasks as assigned. Qualifications and Education Requirements Experience with cold‑chain sample storage and transfer in a GMP regulated environment. Knowledge of basic electronic systems (e.g., email, MS Office) required. Experience with LIMS and ELN computer applications preferred. Ability to lift and carry objects up to 20lbs. Knowledge of regulatory standards as they apply to GMP laboratories preferred. Attention to detail and demonstrated organizational skills. Ability to adapt and adjust to changing priorities and manage multiple assignments with challenging/conflicting deadlines. Ability to work in a high‑paced team environment, meet deadlines, and prioritize work. Effective communication skills with peers, department management, and cross‑functional teams. Bachelor’s degree in Chemistry, Microbiology, or related science with 0–2+ years of relevant work experience, preferably in a regulated environment; or Associate’s degree with 2+ years of relevant experience. Alternate education and experience combinations may substitute. Awareness of biohazardous materials and potential exposure to fluctuating or extreme temperatures. Compensation Overview Devens, MA – $32.18 to $38.99 per hour for a full‑time employee (FTE). Additional incentive cash and stock opportunities may be available and final pay will be based on demonstrated experience. Benefits Health coverage (medical, pharmacy, dental, and vision), wellbeing support programs, financial well‑being plans (401(k), disability, life insurance), work‑life benefits (unlimited paid time off with manager approval, paid national holidays, optional holidays, paid sick time, volunteer days, summer hours flexibility, leaves of absence, global shutdown). Eligibility for specific benefits varies by job and location. Equal Employment Opportunity Statement Bristol Myers Squibb is an equal opportunity employer. We do not discriminate on the basis of age, color, disability, gender, gender identity or expression, genetic information, marital status, national origin, pregnancy, protected veteran status, race, religion, or sex. We accommodate reasonable requests for workplace adjustments for qualified applicants with disabilities. For more information, visit our Accessibility page or contact View email address on click.appcast.io. #J-18808-Ljbffr Bristol-Myers Squibb