Senior Manager, Quality Assurance Material Operations, Cell Therapy
Bristol Myers Squibb
August 14, 2026
Remote friendly (Devens, MA)
United States
Operations
Senior Manager, Quality Assurance Material Operations, Cell Therapy (Devens, MA)
Responsibilities:
- Develop, implement, execute, and sustain quality and material disposition activities in accordance with BMS policies, standards, procedures, and Global cGMP.
- Lead oversight of incoming material visual inspection, disposition, and eSystem master data programs.
- Ensure timely/accurate delivery of disposition requirements from Quality Control and Supply Chain.
- Ensure compliant release of incoming raw materials/consumables; maintain and review SOPs.
- Act as Subject Matter Expert in projects and regulatory inspections.
- Direct quality initiatives for continuous improvement and site manufacturing efficiencies.
- Recognize quality issues/opportunities; provide guidance interpreting complex data.
- Communicate clearly with management; multitask and solve minor-to-moderate issues with limited supervision.
Qualifications / Required Skills:
- Knowledge/experience with cGMP manufacturing, Quality, and compliance.
- Oversight of incoming material inspection and disposition programs.
- Oversight of highly complex eSystem quality master data approvals in ERP and electronic batch record systems (SAP, Syncade MES).
- Ability to hire/train/coach leaders and execute/sustain program work.
- Maintain quality Inspection Plans in SAP; oversee/approve incoming material procedural documentation and new material requests.
- Present/review programs with internal, global, and health authority auditors.
- 8+ years in pharmaceutical or related GMP industry.
- Bachelorβs degree in biological science/engineering or equivalent combination of education/experience.
Benefits (explicitly stated):
- Health coverage (medical, pharmacy, dental, vision), wellbeing support, 401(k), disability and life insurance, and other listed protections.
Apply anyway note:
- If the role doesnβt perfectly match your resume, BMS encourages applying.
Responsibilities:
- Develop, implement, execute, and sustain quality and material disposition activities in accordance with BMS policies, standards, procedures, and Global cGMP.
- Lead oversight of incoming material visual inspection, disposition, and eSystem master data programs.
- Ensure timely/accurate delivery of disposition requirements from Quality Control and Supply Chain.
- Ensure compliant release of incoming raw materials/consumables; maintain and review SOPs.
- Act as Subject Matter Expert in projects and regulatory inspections.
- Direct quality initiatives for continuous improvement and site manufacturing efficiencies.
- Recognize quality issues/opportunities; provide guidance interpreting complex data.
- Communicate clearly with management; multitask and solve minor-to-moderate issues with limited supervision.
Qualifications / Required Skills:
- Knowledge/experience with cGMP manufacturing, Quality, and compliance.
- Oversight of incoming material inspection and disposition programs.
- Oversight of highly complex eSystem quality master data approvals in ERP and electronic batch record systems (SAP, Syncade MES).
- Ability to hire/train/coach leaders and execute/sustain program work.
- Maintain quality Inspection Plans in SAP; oversee/approve incoming material procedural documentation and new material requests.
- Present/review programs with internal, global, and health authority auditors.
- 8+ years in pharmaceutical or related GMP industry.
- Bachelorβs degree in biological science/engineering or equivalent combination of education/experience.
Benefits (explicitly stated):
- Health coverage (medical, pharmacy, dental, vision), wellbeing support, 401(k), disability and life insurance, and other listed protections.
Apply anyway note:
- If the role doesnβt perfectly match your resume, BMS encourages applying.