Senior Cell Therapy Manufacturing Associate – Onsite

Bristol Myers Squibb; United States; On-site; USD 46,000 - 56,000; Full time

Benefits offered by this job

Comprehensive benefits

Flexible time off

11 paid holidays

Job summary

Bristol Myers Squibb (BMS) is seeking a Senior Manufacturing Associate, Cell Therapy for its Devens, MA site. The role focuses on executing GMP-compliant manufacturing operations for cell therapy, including aseptic processing, equipment setup, and training others.

Candidates should have cGMP experience and be able to work day/night shifts, including holidays, in a cleanroom environment. The position offers comprehensive benefits, a strong emphasis on safety and quality, and opportunities to

Qualifications

• Knowledge of cGMP regulations and FDA guidance.
• Ability to work assigned shift (including holidays).
• Cleanroom environment and aseptic processing proficiency.
• Comfort around human blood components and magnets.
• Experience with cell therapy manufacturing and related equipment.

Responsibilities

• Execute operations described in SOPs and batch records.
• Maintain compliance with safety, quality systems, and GMP requirements.
• Complete documentation for process transfers, validations, and batch records.
• Train others on SOPs and work instructions for manufacturing operations.
• Support investigations and identify innovative solutions.
• Assist setup of manufacturing areas and equipment, and perform commissioning activities.
• Collaborate with production planning to execute daily operations across shifts.
• Work in a cleanroom and perform aseptic processing to meet Health Authority requirements.

Skills

cGMP knowledge

Cleanroom experience

Aseptic processing

Cell therapy manufacturing

Shift flexibility

Education

High school diploma + 3+ years cGMP experience

Bachelor's in relevant science or engineering

Tools

Automated equipment

Biosafety cabinets ISO 5

Job description

Bristol Myers Squibb (BMS) is seeking a Senior Manufacturing Associate, Cell Therapy for its Devens, MA site. The role focuses on executing GMP-compliant manufacturing operations for cell therapy, including aseptic processing, equipment setup, and training others.

Candidates should have cGMP experience and be able to work day/night shifts, including holidays, in a cleanroom environment. The position offers comprehensive benefits, a strong emphasis on safety and quality, and opportunities to