Senior Bioprocess Operator - Night Shift

Bristol Myers Squibb EU Policy; Harvard (MA); On-site; USD 41,000 - 50,000; Full time

Benefits offered by this job

Comprehensive benefits

Flexible time off (FTO)

11 paid company holidays

Job summary

Bristol Myers Squibb EU Policy is seeking a Senior Bioprocess Associate for a night-shift role in Devens, MA. You will execute commercial manufacturing processes for therapeutic proteins under cGMPs, operate bioreactors, chromatography skids and support process automation systems, ensuring compliance and quality.

The role emphasizes adherence to GMP, SOPs, and safe work practices, with opportunities for process improvement and cross-functional collaboration within the manufacturing team.

Qualifications

• High school diploma required; B.S. in science, engineering, biochemistry or related discipline preferred but not required.
• Minimum of 2+ years of process operations experience in a GMP biotech facility.
• Knowledge of GMP and SOPs; prior experience in teamwork with accountability and attention to detail.
• Proficiency with common computer tools (word processing, spreadsheets, web apps).
• Demonstrates good interpersonal skills and professional relationships with management and coworkers.

Responsibilities

• Perform routine manufacturing tasks per procedures with minimal instructions.
• Follow GMP and SOPs; maintain clean room and regulatory compliance.
• Revise/create process documents and assist investigations.
• Train in process automation and operation of production equipment.
• Maintain inventory levels of materials and components.

Skills

GMP knowledge

SOP knowledge

Attention to detail

Team collaboration

Process automation

Regulatory compliance

Bioprocess operations

Education

High school diploma

B.S. in science/engineering/biochemistry

Tools

DeltaV

Syncade

OSI/Pi Historian

SAP

Trackwise

Maximo

Job description

Bristol Myers Squibb EU Policy is seeking a Senior Bioprocess Associate for a night-shift role in Devens, MA. You will execute commercial manufacturing processes for therapeutic proteins under cGMPs, operate bioreactors, chromatography skids and support process automation systems, ensuring compliance and quality.

The role emphasizes adherence to GMP, SOPs, and safe work practices, with opportunities for process improvement and cross-functional collaboration within the manufacturing team.