Cellares
Director, Quality Compliance
Bridgewater, NJ · Director
Sponsorship not specified$90k-$250kDetected 60 days ago
GMP
About the role
- This individual will be responsible for leading Quality Compliance activities for the Bridgewater site.
- They will be identifying and assessing regulatory and quality risks during site GMP operations ensuring adherence to global regulations and Cellares' policies and procedures.
- This individual will be responsible for leading the continuous inspection readiness efforts and the site's self-inspection program.
Responsibilities
- They will manage routine use of the Cellares Quality Management Systems.
- The company is both developing and operating integrated technologies for cell therapy manufacturing to accelerate access to life-saving cell therapies.
Compensation
- $90k-$250k
Benefits
- The company's Cell Shuttle integrates all the technologies required for the entire manufacturing process in a flexible and high-throughput platform that delivers true walk-away, end-to-end automation.
- Leveling will be based on overall experience, education, and demonstration of knowledge throughout the interview process.
Company info
- We are seeking an innovative and highly motivated Director, Quality Compliance, who will contribute significantly to the growth of the Cellares team.
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