Up-to-date knowledge of pharmaceutical product release, stability testing, analytical method validation, analytical method transfer and compendial method verification as per current regulatory standards. * Maintain daily contact with the of non-chromatographic release and IPC labs to ensure optimal support for testing laboratories. * Liaise with relevant organizations, such as QA, chemical production, R&D, CMC RA and build a network of contacts to support troubleshooting. * Independently prepare, finalize, and/or review GMP procedures applicable to non-chromatographic laboratories of the QC. * Develop fit-for-purpose standards and guidelines applicable to the QC analytical laboratory to achieve both scientific excellence and regulatory compliance in a commercial QC environment where New Product Introduction is in strategic focus.
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