QA Operations Lead — Cell Therapy Materials

Bristol-Myers Squibb; Massachusetts; On-site; USD 130,000 - 158,000; Full time

Benefits offered by this job

Health Coverage

Wellbeing Support

Financial protection

Paid Time Off

Job summary

Bristol Myers Squibb seeks a Senior Manager of Quality Assurance Material Operations for Cell Therapy at the Devens, MA facility. You will lead QA material disposition, ensure cGMP compliance, and drive data integrity across ERP and eSystem master data programs.

You will coach a team, interact with cross-functional groups, and prepare documentation for regulators and internal stakeholders. This role emphasizes risk-based decision making and continuous improvement.

Qualifications

• A minimum of 8 years of experience in the pharmaceutical or related GMP industry.
• Bachelor's degree in biological science, engineering, or similar.
• Experience with material inspection, disposition programs, and SAP/MES master data.
• Experience supervising a team of individual contributors and first-line leaders.

Responsibilities

• Oversee incoming material inspection and disposition programs.
• Manage eSystem quality master data approvals in ERP and SAP and Syncade MES.
• Hire, train, and coach staff to sustain programs.
• Represent Devens facility in network initiatives and audits.

Skills

cGMP manufacturing

Quality oversight

Problem solving

Leadership

Education

Bachelor's degree in biological sciences or engineering

Tools

SAP

Syncade MES

Job description

Bristol Myers Squibb seeks a Senior Manager of Quality Assurance Material Operations for Cell Therapy at the Devens, MA facility. You will lead QA material disposition, ensure cGMP compliance, and drive data integrity across ERP and eSystem master data programs.

You will coach a team, interact with cross-functional groups, and prepare documentation for regulators and internal stakeholders. This role emphasizes risk-based decision making and continuous improvement.