Cellares
Manager, Quality Control
Bridgewater, NJ
Sponsorship not specified$90k-$210kDetected 33 days ago
ExcelAuditingGMPMolecular BiologyCommunicationMicrosoft Office
About the role
- This position will work with the Quality Control team in supporting our efforts in the GMP manufacturing of cellular therapy products.
- This role will report to the Senior Director of Quality Control.
- Cell Shuttles will be deployed in Cellares' Smart Factories around the world to meet total patient demand for cell therapies at global scale.
Responsibilities
- This individual will lead a group of QC analysts performing analytical testing of in-process and final product from cell therapy products.
- They will interface across different parts of the company to support novel products used in cell and gene therapy.
Requirements
- Minimum of 7 years experience in a cGMP or cGxP at an operational level supporting manufacturing in a pharmaceutical or biotech environment
- At least 2 years in a managerial role
- Strong working knowledge of quality systems and regulatory requirements including 21 CFR Part 11/210/211
- Must have working knowledge of controlled documentation, data systems, cGMPs, SOPs, analytical testing, and auditing
Nice to have
- M.S. in a scientific discipline is preferred
- Prior experience related to method development/validation preferred
- BA or B.S. degree in a science discipline required, or comparable experience
Compensation
- $90k-$210k
Benefits
- Self-awareness, integrity, authenticity, and a growth/entrepreneurial mindset
Company info
- We are seeking an innovative and highly motivated individual to join our team as the Manager of Quality Control at our GMP manufacturing facility located in Bridgewater, NJ.
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This listing is sourced directly from Cellares's careers page and normalized into a canonical job model.