Maintain daily contact with the of non-chromatographic release and IPC labs to ensure optimal support for testing laboratories. * Drive systematic changes in QC non-chromatographic area, create and assess change controls, facilitate implementation plan. * 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. * Act as SME for non-chromatographic analytical technologies and provide scientific oversight * Drive complex scientific / quality investigations in your field in a cross-functional team and facilitate related remediation plans (e.g., CAPA plan). * Liaise with relevant organizations, such as QA, chemical production, R&D, CMC RA and build a network of contacts to support troubleshooting.
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