The Manager Manufacturing will be responsible for managing the manufacturing and import of medicinal products and investigational medicinal products in compliance with §12 AMWHV, GMP, and regulatory requirements. This role ensures timely batch review, product testing, documentation, and release to the Qualified Person, while helping to maintain GMP-compliant facilities, partners/suppliers and optimized processes. This person collaborates and actively works within Quality Assurance to manage deviations, CAPA, audits, and regulatory compliance.