GMP Bioprocess Operator for Therapeutic Proteins

Bristol-Myers Squibb Company; Harvard (MA); On-site; USD 35,000 - 42,000; Full time

Benefits offered by this job

Flexible Time Off

11 paid holidays

Volunteer days

Stock opportunities

Job summary

Bristol Myers Squibb is seeking a Bioprocess Associate for our Devens, MA site. You will perform commercial manufacturing of therapeutic proteins under cGMP, following SOPs and safety protocols.

The role involves operating production equipment, maintaining inventory, and supporting process documentation and investigations to ensure quality and compliance. The position emphasizes training in process automation, collaboration across teams, and adherence to GMP standards in a regulated

Qualifications

• Minimum high school diploma; associate-level biotechnology degree preferred.
• Experience with GMPs and clean rooms or highly regulated environments is desirable.
• Proficiency with common computer tools and web-based applications.

Responsibilities

• Operate production equipment per GMPs and SOPs.
• Revise and create process documents and assist investigations.
• Train for proficiency in process automation and production equipment.
• Lead in maintaining material and components inventory.
• Support a safe work environment and contribute to area initiatives.
• Weigh and check raw materials; assemble, clean and autoclave components.
• Assist in maintaining inventory and performing routine manufacturing tasks.
• Assist in revising SOPs and batch records and in process investigations.

Skills

GMP compliance

SOP procedures

Process automation

Attention to detail

Team collaboration

Education

High school diploma

Associates Degree in Biotechnology

Tools

Process automation software

Business systems

Job description

Bristol Myers Squibb is seeking a Bioprocess Associate for our Devens, MA site. You will perform commercial manufacturing of therapeutic proteins under cGMP, following SOPs and safety protocols.

The role involves operating production equipment, maintaining inventory, and supporting process documentation and investigations to ensure quality and compliance. The position emphasizes training in process automation, collaboration across teams, and adherence to GMP standards in a regulated