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Certify medicinal products to EU requirements, provide quality and compliance guidance, oversee QMS elements (CAPAs, deviations, change controls), ensure manufacturing/packaging documentation, support investigations and audits, advise cross-functional teams, maintain GMP/GDP knowledge, and support continuous improvement and regulatory readiness.

The Project Manager will lead CQV projects, ensuring compliance and timely execution, manage project documentation, and coordinate with stakeholders.

Support quality and compliance for commercial manufacturing: perform batch record review and disposition, oversee certification, manage deviations and investigations, apply cGMP and regulatory requirements, use SAP/Trackwise, and drive continuous improvement of Quality Systems.

The Process Engineer will manage small-to-medium scale projects, specify process equipment, revise diagrams, support QA Validation, and ensure compliance with regulations.