Manage the manufacturing and import of medicinal products and investigational medicinal products in compliance with Β§12 AMWHV, GMP, and regulatory requirements. Ensure timely batch review, product testing, documentation, and release to the Qualified Person, while helping to maintain GMP-compliant facilities, partners/suppliers and optimized processes. Collaborate within Quality Assurance to manage deviations, CAPA, audits, and regulatory compliance.
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