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ElevateBio is looking for a Specialist II, QA Operations to join their growing Quality Group at our BaseCamp facility in Waltham, MA. In this role, the Specialist II will be primarily responsible for providing Quality oversight over execution of clinical cell and gene therapy manufacturing for cGMP compliance through on the production floor interactions, review and approval of batch related documents, and events. This individual will engage with other members within operational departments as a Quality partner by providing real-time support in order to achieve on-time closure of quality records. A successful candidate in this position will effectively execute complex assignments, apply knowledge of best practices of cGMP to define solutions, and has subject matter expertise within Quality related functions.
