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You will ensure that our suppliers and external partners meet the highest quality and compliance standards - while enabling innovation, efficiency, and sustainable growth. You’ll operate as a key expert within our Quality organization, influencing
Provide end-to-end QA oversight of DP, IMP manufacturing activities internally and at CMOs, ensuring sustained GMP compliance and supply continuity for clinical trials. Ensure batch release within delegated authority in accordance with applicable GMP
Ensure compliance with international quality standards and regulatory requirements. Participation in regulatory inspections and external audits. Support the planning and execution of internal audits. Support with document control activities, including
The role is responsible for leading and developing the medical team, driving innovation, ensuring scientific excellence, regulatory compliance, and strong cross‑functional collaboration to support pre‑ and post‑launch activities across the