The Quality Assurance Shop Floor (QASF) organization is responsible for quality oversight and advising on quality operations at the Devens Cell Therapy Facility in accordance with BMS policies, standards, procedures, and Global current Good Manufacturing Practices (cGMPs)
Job Summary
The Quality Assurance Shop Floor (QASF) organization is responsible for quality oversight and advising on quality operations at the Devens Cell Therapy Facility in accordance with BMS policies, standards, procedures, and Global current Good Manufacturing Practices (cGMPs).
The Manager will handle internal compliance and documentation tasks, routine communication to front-line employees, and metrics/monitoring for key QASF processes, acting as a local process owner for core QASF systems.
Bristol Myers Squibb offers a wide variety of competitive benefits, services, and programs that provide employees with the resources to pursue their goals, both at work and in their personal lives.
Matching Summary
The Quality Assurance Shop Floor (QASF) organization is responsible for quality oversight and advising on quality operations at the Devens Cell Therapy Facility in accordance with BMS policies, standards, procedures, and Global current Good Manufacturing Practices (cGMPs).
Salary
Base: $100,480 - $121,756; Bonus/Equity: Additional incentive cash and stock opportunities may be available; Benefits: Health Coverage, Wellbeing Support, Financial Well-being and Protection, Work-life benefits
Skills & Requirements
Must-have
Quality oversight of cell therapy facility
cGMP compliance and documentation
Process ownership for QASF systems
GxP record review and approval
Stakeholder relationship management
On-the-floor quality oversight
Nice-to-have
Psychological and physical safety champion
Teamwork and continuous improvement culture
Pioneering mindset and innovative solutions
Coaching and mentoring operators
Key Requirements
6+ years of relevant cGMP experience
2+ years of QA shop floor experience
Bachelor's degree in STEM field preferred
Experience with GxP electronic systems
FDA/EMA regulations in biopharmaceuticals or cell therapy manufacturing preferred