Support compliance with all relevant and appropriate regulations and guidelines, such as those relating to GMP/GDP, health and safety, etc. * Support in-licensing activities by providing Quality Assurance expertise for the evaluation of new project opportunities including participation in due diligence activities. * Support the systems and processes in place for the appropriate documentation of the company development activities and to maintain them in a manner compliant with regulatory and corporate requirements. * Ensure the Clinical Supply Quality activities are consistent across the range of different environments and teams supported (Vendors / / in house). * Proactively support the activities of Clinical supply for relevant manufacturing quality systems (deviation close out / Cha
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