Training Specialist, Cell Therapy Manufacturing in Devens, MA
Job in
Harvard, Worcester County, Massachusetts, 01451, USA
Listed on 2026-07-18
Listing for:
Bristol-Myers Squibb
Full Time
position Listed on 2026-07-18
Job specializations:
-
Manufacturing / Production
Pharmaceutical Manufacturing, Manufacturing & Industrial Operations
Job Description & How to Apply Below
Training Specialist, Cell Therapy Manufacturing
Location:
Devens, MA, USA
Job : R1604362
Shift: Monday – Thursday, 1pm – 11pm
CompensationHourly: $35.50 – $43.02. Additional incentive cash and stock opportunities may be available.
Responsibilities- Demonstrate the ability to execute operations as described in standard operating procedures and batch records.
- Show strong practical and theoretical knowledge in the work performed.
- Complete documentation required by training policies and standard operating procedures.
- Perform and demonstrate tasks in a manner consistent with safety policies, quality systems, and GMP requirements.
- Qualify new employees on the assigned curriculum required for their job functions.
- Execute trainee re‑qualification as needed.
- Ensure on‑time completion of training assignments so technical skills and knowledge are adequate before training other individuals.
- Collaborate with support groups on recommendations and solve training gaps between new‑hire onboarding and transition to manufacturing operations.
- Identify innovative solutions.
- Support creation of manufacturing training materials such as on‑the‑job trainings and instructor‑led trainings.
- Work independently, escalates issues appropriately, and collaborates with management to resolve them.
- Knowledge of cGMP regulations and FDA guidance applicable to biologics and cell therapy manufacturing.
- Ability to gown into a cleanroom environment.
- Comfortable working near strong magnets.
- Experience delivering training to adult learners and groups.
- Experience and knowledge of cell therapy operations preferred.
- Effective communication with peers, trainees, and cross‑functional stakeholders.
- Collaboration with employees at all levels.
- Strong problem‑solving and critical‑thinking skills.
- 4+ years of experience in cGMP bioprocessing manufacturing, cell therapy manufacturing, or relevant experience.
- Bachelor’s degree in a relevant science or engineering discipline, or equivalent work experience.
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