Cell Therapy Specialist II
The Cell Therapy Specialist II supports the successful tech transfer and operational readiness process. The CTS II will use knowledge of cGMP regulations and project management to ensure manufacturing readiness. Responsibilities of primary importance are to ensure the successful time sensitive GMP manufacture and release of cell therapy products and promote a culture of quality and compliance. Ensure all processes and procedures related to operations are in full compliance with cGMP, CFR and site quality systems and company policies. Upon start of clinical manufacturing the CTS II will be part of a cohesive team responsible for Deviations, CAPAs, Change Controls and is expected to be able to work independently with minimal supervision.
*The company reserves the right to add or change duties at any time.
Job Qualifications & Skills
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