Cell Therapy Manufacturing Associate II

Bristol Myers Squibb; Massachusetts; On-site; USD 41,000 - 50,000; Full time

Job summary

Bristol Myers Squibb is seeking a Clinical Manufacturing Associate II, Cell Therapy in Devens, MA. The role emphasizes cGMP manufacturing, aseptic processing, and collaboration across teams to support startup activities and ongoing operations.

The position requires a high school diploma with 2+ years in cGMP bioprocessing or related fields, with a preference for a science/engineering bachelor’s degree and GMP data integrity knowledge. On-site work with comprehensive benefits is provided.

Qualifications

• High school diploma and 2+ years of experience in cGMP bioprocessing manufacturing, cell therapy manufacturing or relevant experience.
• Bachelor’s degree in science or engineering is preferred; GMP compliance experience is valued.
• Knowledge of data integrity concepts (ALCOA+) and aseptic processing in ISO 5 environments is preferred.

Responsibilities

• Perform clinical patient process unit operations per SOPs and batch records.
• Maintain cGMP compliance and quality systems in manufacturing.
• Complete documentation per batch records, SOPs and work instructions.
• Operate in cleanroom environments and perform aseptic processing.
• Collaborate with support groups to troubleshoot technical and operational issues.
• Assist in setting up manufacturing areas and equipment; participate in facility commissioning.

Skills

cGMP knowledge

cell therapy manufacturing

cleanroom work

shift flexibility

travel to train

Education

High school diploma

Bachelor’s degree preferred in science/engineering

GMP compliance training

Job description

Bristol Myers Squibb is seeking a Clinical Manufacturing Associate II, Cell Therapy in Devens, MA. The role emphasizes cGMP manufacturing, aseptic processing, and collaboration across teams to support startup activities and ongoing operations.

The position requires a high school diploma with 2+ years in cGMP bioprocessing or related fields, with a preference for a science/engineering bachelor’s degree and GMP data integrity knowledge. On-site work with comprehensive benefits is provided.