Accordingly, the candidate is responsible for executing the technology transfer in accordance with the established standard processes to facilitate alignment of tech transfer and validation activities across the projects for Drug Product manufacturing, evaluates CMC risks for appropriate escalation, recommends transition milestones and ensures a smooth transition of projects, recommends, and implements new technologies, as needed and supports Supply Chain Management with technical issues during routine commercial production. * Excellent knowledge of CMC development, process development and technology transfer, CMC regulatory, and GMP compliance in the field of small molecule solids and/or biologics parenteral formulations
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