Supply Chain Operator, Cell Therapy
Listed on 2026-06-30
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Quality Assurance - QA/QC
Production QC/QA
Supply Chain Operator, Cell Therapy Shifts Available
Day Shift: 6am - 6pm, rotational schedule including holidays and weekends.
Responsibilities- Performs cGMP functions associated with packaging operations, including visual inspection, labeling, and cartoning to support operations described in standard operating procedures and batch records.
- Performs receiving transitions for patient and/or healthy donor samples and shipments for finished goods product.
- Performs room sanitization activities to maintain controlled environment compliance.
- Completes documentation required by process transfer protocols, validation protocols, standard operating procedures, and batch records.
- Performs tasks consistently with the safety policies, quality systems, and GMP requirements.
- Completes training assignments to ensure the necessary technical skills and knowledge.
- Assists in setting up packaging manufacturing areas and equipment/fixtures, and performs facility and equipment commissioning activities.
- Trains others on SOPs and work instructions to successfully complete product packaging operations.
- Executes daily unit operations schedule that includes people, product, and material flow across multiple shifts.
- Additional duties, tasks, and responsibilities as assigned by the Supply Chain department.
- Experience with electronic batch records preferred.
- Driven and motivated individual eager to learn and execute final product packaging operations.
- Must be able to work assigned shift (Day or Night).
- Must be able to work flexible hours, including weekends and/or holidays, to complete work activities.
- Must be able to work in a clean room environment and perform final product packaging.
- Must be comfortable being exposed to human blood components.
- Must be able to work with temperature‑controlled products.
- Receiving and shipping experience is a plus.
- Knowledge of inventory systems preferred.
- Proficiency in reading, writing, and verbally communicating in English.
- Knowledge of cGMP regulations and FDA guidance applicable to biologics and cell therapy manufacturing is preferred.
- High school diploma and or GED equivalency.
- 1-3 years of experience in cGMP manufacturing within a biopharmaceutical or related field.
Devens – MA – US: $30.81 – $37.33 per hour. The starting compensation range(s) for this role are listed above for a full‑time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job‑related knowledge, and experience.
Final, individual compensation will be decided based on demonstrated experience.
- 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 (EAP). - 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.
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 Visit to access our complete Equal Employment Opportunity statement.
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R1603186 :
Supply Chain Operator, Cell Therapy
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