Night-Shift Bioprocess Associate – GMP Manufacturing

Biopharma Careers; Harvard (MA); On-site; USD 85,475,000 - 103,584,000; Full time

Job summary

Bristol Myers Squibb in Devens, MA is seeking a Senior Bioprocess Associate to execute cGMP manufacturing for therapeutic proteins. The role covers batch records, SOPs, and equipment like bioreactors and chromatography skids, with night shifts.

You will work in a collaborative team, ensure quality, safety, and compliance, and use DeltaV, Syncade, SAP, and TrackWise to maintain production records.

Qualifications

• High school diploma is required; a BS in science/engineering/biochemistry or related field is preferred.
• Experience with cGMP operations and SOPs in biotech manufacturing.
• Strong attention to detail and ability to work in teams with accountability.
• Proficient with common computer tools and production documentation.

Responsibilities

• Execute routine manufacturing assignments per procedures with minimal supervision.
• Adhere to GMP standards and SOPs; revise batch records as needed.
• Operate bioreactors, chromatography skids, and related production equipment.
• Maintain inventory levels and support area safety initiatives.
• Use automation systems (DeltaV, Syncade) and business systems (SAP, TrackWise, Maximo) for records.

Skills

Attention to detail

Collaboration

Teamwork

Accountability

Education

B.S. in science/engineering/biochemistry or related

High school diploma

Tools

DeltaV

Syncade Interactions

OSI/Pi Historian

SAP

TrackWise

Maximo

Job description

Bristol Myers Squibb in Devens, MA is seeking a Senior Bioprocess Associate to execute cGMP manufacturing for therapeutic proteins. The role covers batch records, SOPs, and equipment like bioreactors and chromatography skids, with night shifts.

You will work in a collaborative team, ensure quality, safety, and compliance, and use DeltaV, Syncade, SAP, and TrackWise to maintain production records.