Able to lead QC operations and handling regulatory issues for international and national dossiers. Able to responsible for evaluating analytical information, validate outcomes and COAs to make sure compliance. Able to manage OOT, deviations, OOS and change controls.
Strong knowledge of analytical techniques like UV, IR, HPLC and pharmaceutical protocols, with mindfulness of ISO 17025. Candidate must have M.Sc. Degree in Chemistry or Pharm-D from any reputed university.
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