Bioprocess Associate
Bristol Myers Squibb
September 03, 2026
Remote friendly (Devens, MA)
United States
Operations
Position Summary:
- The Bioprocess Associate uses current Good Manufacturing Practices (cGMPs) in the execution of commercial manufacturing processes for therapeutic proteins.
Key Responsibilities:
- Operate production equipment in an assigned functional area in accordance with GMPs and SOPs.
- Revise/create process documents and assist with process-related investigations.
- Train for proficiency in process automation, supporting business systems, and primary production equipment operations.
- Maintain material and components inventory levels.
- Support a safe work environment and area-specific work safety initiatives.
- Weigh and check raw materials.
- Assemble, clean, and autoclave process components.
- Perform routine manufacturing assignments per written procedures with minimal instructions.
- Assist in revising/creating SOPs and Batch Records and support process-related investigations.
Qualifications & Experience:
- Minimum high school diploma required; science knowledge via certificate program or Associates Degree in Biotechnology or related field desired.
- Prior experience with GMP regulations and/or clean room/highly regulated environment desired.
- Experience working on teams requiring personal accountability, attention to detail, collaboration, and results.
- Proficiency with common computer tools and web-based applications.
Compensation (Devens, MA, US):
- $25.34–$30.70 per hour (full-time). Additional incentive opportunities may be available (eligibility-based).
- The Bioprocess Associate uses current Good Manufacturing Practices (cGMPs) in the execution of commercial manufacturing processes for therapeutic proteins.
Key Responsibilities:
- Operate production equipment in an assigned functional area in accordance with GMPs and SOPs.
- Revise/create process documents and assist with process-related investigations.
- Train for proficiency in process automation, supporting business systems, and primary production equipment operations.
- Maintain material and components inventory levels.
- Support a safe work environment and area-specific work safety initiatives.
- Weigh and check raw materials.
- Assemble, clean, and autoclave process components.
- Perform routine manufacturing assignments per written procedures with minimal instructions.
- Assist in revising/creating SOPs and Batch Records and support process-related investigations.
Qualifications & Experience:
- Minimum high school diploma required; science knowledge via certificate program or Associates Degree in Biotechnology or related field desired.
- Prior experience with GMP regulations and/or clean room/highly regulated environment desired.
- Experience working on teams requiring personal accountability, attention to detail, collaboration, and results.
- Proficiency with common computer tools and web-based applications.
Compensation (Devens, MA, US):
- $25.34–$30.70 per hour (full-time). Additional incentive opportunities may be available (eligibility-based).