NIGHT SHIFT: Senior Manufacturing Associate, Cell Therapy in Devens, MA

Senior Manufacturing Associate, Cell Therapy Location: Devens, MA Shift Information 6pm – 6am rotating shift, including holidays and weekends, onsite. Responsibilities Execute operations described in standard operating procedures and batch records. Demonstrate strong practical and theoretical knowledge in their work. Complete documentation required by process transfer protocols, validation protocols, standard operating procedures, and batch records. Solve simple problems and take new perspectives using existing solutions. Perform tasks in a manner consistent with safety policies, quality systems, and GMP requirements. Complete training assignments to ensure the necessary technical skills and knowledge. Train others on SOPs and Work Instructions to successfully complete manufacturing operations. Support investigations. Identify innovative solutions. Assist in setting up manufacturing areas and equipment/fixtures; perform facility and equipment commissioning activities. Write manufacturing operating procedures that are technically sound, promote effective and efficient operations, and comply with cGMP requirements. Work with production planning to execute daily unit operations schedules that include people, product, and material flow across multiple shifts. Work in a cleanroom environment and perform aseptic processing; maintain manufacturing environmental conditions (non‑viable particulate and viable microbial levels per controlled area classification specifications) by performing area disinfection regimens as required to meet global Health Authority requirements. Knowledge and Skills Knowledge of cGMP regulations and FDA guidance applicable to biologics and cell therapy manufacturing. Ability to work assigned shift (day, night, weekends and/or holidays). Ability to work in a cleanroom environment and perform aseptic processing. Comfortable being exposed to human blood components. Ability to be in close proximity to strong magnets. Experience in cell therapy manufacturing, including cell washing processes, automated equipment, cell separation techniques, and cryopreservation processes. Experience with aseptic processing in ISO 5 biosafety cabinets and universal precautions for handling human‑derived materials in BSL‑2 containment areas. Experience in cell expansion using incubators and single‑use bioreactors. Basic Requirements High school diploma and 3+ years of experience in cGMP bioprocessing manufacturing, cell therapy manufacturing, or relevant experience. Bachelor’s degree in a relevant science or engineering discipline and relevant experience is strongly preferred. Working Conditions Stand and walk while operating manufacturing/computer equipment for several hours at a time, throughout the day. Carry, lift, push, and pull up to 50 lb several times a day while handling production equipment and/or materials. Climb using stepladders in production areas or stairwells several times a day. Bend or kneel several times a day. Perform overhead reaching during handling of production materials/files/supplies up to 25 lb several times a day. Move head and neck while using computer applications and handling production equipment and materials several times a day. Twist waist while setting up equipment several times a day. Repetitive use of arms, wrists, and hands while setting up equipment and processing several times a day. Wear personal protective equipment (PPE) and other clean‑room garments daily; this may include safety shoes, safety glasses, aprons, face shields, lab coats, full‑body gowns, hairnets, gloves, and hearing protection. Compensation Overview US $33.51 – $40.61 per hour (full‑time employee). Additional incentive cash and stock opportunities may be available. Final compensation will be based on demonstrated experience. Candidate Rights BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. #J-18808-Ljbffr Bristol Myers Squibb