Senior Bioprocess Specialist – GMP Manufacturing

Bristol-Myers Squibb Company; Harvard (MA); Sur place; USD 41 000 - 50 000; Plein temps

Avantages offerts par ce poste

Flexible Time Off

11 paid holidays

Volunteer days

Résumé du poste

Bristol Myers Squibb is hiring a Senior Bioprocess Associate in Devens, MA to execute commercial manufacturing of therapeutic proteins under cGMPs. The role emphasizes adherence to procedures, process documentation, and safe operation of bioreactors and chromatography systems.

You will support process automation, train on production systems, and assist with batch records while ensuring quality and regulatory compliance.

Qualifications

• High school diploma required; science background or equivalent desired.
• 2+ years in GMP biotech process operations.
• Attention to detail and teamwork are essential.
• Proficiency with common office tools and web-based apps.

Responsabilités

• Execute routine manufacturing per procedures with minimal instructions.
• Adhere to cGMPs and SOPs; support process docs and investigations.
• Operate bioreactors, chromatography skids, and prep equipment.
• Maintain inventory and participate in area safety initiatives.
• Review batch/exception reports with supervisor and QA.

Connaissances

Attention to detail

Collaboration

Interpersonal skills

Formation

High school diploma

B.S. in science/engineering/biochemistry

Outils

DeltaV

Syncade

OSI/Pi Historian

SAP

Description du poste

Bristol Myers Squibb is hiring a Senior Bioprocess Associate in Devens, MA to execute commercial manufacturing of therapeutic proteins under cGMPs. The role emphasizes adherence to procedures, process documentation, and safe operation of bioreactors and chromatography systems.

You will support process automation, train on production systems, and assist with batch records while ensuring quality and regulatory compliance.