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GMP Facility Operations Specialist
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We are seeking an experienced GMP Facility Operations Specialist to join our team at CRIS. In this role, you will be responsible for overseeing the day-to-day operations of our GMP facility, ensuring that all activities are conducted in accordance with GMP guidelines and regulations.
Key Responsibilities:
- Oversee production of cell-based therapy products in CRIS' GMP facility
- Ensure compliance to Good Manufacturing Practice (GMP) guidelines and relevant safety requirements
- Manage all aspects of laboratory operations, including planning production schedules and resolving operational issues
- Collaborate with other functions to facilitate new product introduction and technology transfer of CRIS projects
- Participate in the development of new manufacturing processes and process improvements