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https://careers.evonik.com/en/about/meet-the-team/ Responsibilities Maintain and revise QA related procedures, as needed. Maintain cGMP training systems and perform on-site team member training in Quality related matters Ensure GxP support and oversight, as applicable, for relevant site functions and activities Support QA team members with Senior QA level knowledge, experience, guidance, coaching and mentoring, as required Perform QA batch record review and disposition of manufactured early phase clinical product batches. Provide final QA approval of investigations and disposition of any impac

179 Open Roles

179 open roles · apply directly
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