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.
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The Senior Supplier Quality Manager will support the management a group of globally based, experienced professionals and leads complex and strategic initiatives in collaboration with other Convatec Senior leaders. The Global Supplier Quality teams are accountable for developing, deploying and executing global policies and procedures that ensure Convatec business units are harmonized and compliant to the appropriate regulations and standards.