Opportunity Description
We are currently looking for a Quality & Regulatory Affairs Director to ensure the effective management of Quality, Regulatory Affairs and Pharmacovigilance activities across the Asia Pacific region, covering Biopharma, Diagnostics and Healthcare Solutions.
The Quality & Regulatory Affairs Director is a key member of the regional organization and acts as the Responsible Person as defined by local regulations. This role is responsible for maintaining the Quality Management System in compliance with company SOPs, local regulatory requirements, and international GDP/GMP standards, while also leading and developing the local QRA team.
You will act as the technical reference in the country, representing Grifols before health authorities, collaborating closely with HQ, and ensuring compliance across third‑party logistics providers and local operations.
What you will do
- Define and execute regulatory strategies for new and existing ...
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