Cellares
Cell Therapy Manufacturing Specialist
Bridgewater, NJ
Sponsorship not specifiedDetected 495 days ago
GMP
About the role
- Candidates should enjoy working in a fast-paced, mission-driven environment, and be prepared to tackle a broad selection of challenges as the company grows.
Responsibilities
- Perform routine procedures following written instructions (SOPs, batch records, solution documents, protocols, etc.)
- Provide user feedback to engineering and process teams, support with requirements gathering and review
- Support reagent preparation, leukopak processing, and sample testing in an R&D and GMP environment
- Perform routine clean room and laboratory activities including ordering, cleaning, restocking, and equipment qualification/maintenance
- Operate in a controlled GMP environment and perform gowning as per procedure
- Initiate and support the closure of Deviation Reports and CAPAs
- Review in-process and completed documents for accuracy and to make sure batch records are turned in to area management within specified days of completion
Requirements
- Complete required training and ensure compliance with established internal and external control procedures
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This listing is sourced directly from Cellares's careers page and normalized into a canonical job model.