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You lead the site Quality organization and serve as the key authority for GMP compliance and quality strategy. In this executive leadership role, you shape the site’s quality culture while enabling the successful delivery of innovative therapies,
The Manager will handle site-level Quality System compliance, ensuring full compliance of the site quality System with US FDA, ISO 13485, MDSAP/MDR and other applicable country specific regulatory requirements. Specific focus will be
You will combine strategic leadership with hands-on execution. You will be responsible for designing, building, and leading the clinical operations function, while directly overseeing early-phase clinical trials. Lead the strategic planning and execution
This pivotal role is responsible for maintaining supply chain integrity and product quality across API, cosmetics, drugs, devices, components, and finished products. You will be central to ensuring operational excellence, regulatory compliance, and
In this role, the candidate will represent RA in the Clinical Trial Teams and work closely with the CRO and internal stakeholders to ensure regulatory oversight and progress of the clinical trial submissions in EU/ROW. The candidate may also