Sr Manufacturing Associate, Cell Therapy - Devens MA
About The Position
Bristol Myers Squibb Cell Therapy Manufacturing is seeking a Senior Manufacturing Associate to support routine cell therapy manufacturing operations. The role calls for enthusiasm, intellectual curiosity, scientific rigor, flexibility, and a goal-oriented approach, with safety and quality in mind and a good understanding of good manufacturing practices. This is an onsite position in Devens, Massachusetts, with a rotating 6 a.m.–6 p.m. shift that includes holidays and weekends. The associate works in a cleanroom and performs aseptic processing while helping maintain manufacturing environmental conditions in accordance with controlled-area specifications and global Health Authority requirements.
Requirements
- Good understanding of good manufacturing practices.
- Ability to work efficiently with safety and quality in mind.
- Goal-oriented and flexible approach.
- Ability to demonstrate practical and theoretical knowledge in the work.
- Ability to solve simple problems and apply new perspectives using existing solutions.
Responsibilities
- Execute operations described in standard operating procedures and batch records.
- Complete documentation required by process transfer protocols, validation protocols, standard operating procedures, and batch records.
- Perform tasks consistently with safety policies, quality systems, and GMP requirements.
- Complete training assignments to develop the technical skills and knowledge required for the role.
- Train others on SOPs and work instructions so they can successfully complete manufacturing operations.
- Support investigations and identify innovative solutions.
- Assist in setting up manufacturing areas and equipment or fixtures.
- Perform facility and equipment commissioning activities.
- Write technically sound manufacturing operating procedures that promote effective and efficient operations and comply with cGMP requirements.
- Work with production planning to execute the daily unit operations schedule, including people, product, and material flow across multiple shifts.
- Work in a cleanroom and perform aseptic processing.
- Maintain manufacturing environmental conditions, including non-viable particulate and viable microbial levels per controlled-area classification specifications, by performing area disinfection as required.
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What This Job Offers
Job Type
Full-time
Career Level
Senior
Education Level
No Education Listed
