About the role
Lead quality assurance for a GMP-regulated pharmaceutical manufacturing site.
Lead quality assurance for a GMP-regulated pharmaceutical manufacturing site. This role is based on site in Cork, Ireland. The successful candidate will join the operations team and work closely with senior stakeholders.
Responsibilities
- Own the site quality management system
- Lead deviation, CAPA and change-control processes
- Prepare for and host regulatory inspections
- Approve batch documentation and release activities
Requirements
- 7+ years in pharmaceutical quality assurance
- Strong knowledge of EU GMP
- Experience hosting HPRA or FDA inspections