Summary from listing
The role leads the pharmaceutical quality system across GMP-relevant areas at a manufacturing site, driving compliance with international GMP, FDA, EMA, ICH, and ISO requirements. Responsibilities include managing quality events, CAPA implementation, quality investigations, quality committee meetings, KPI reporting, and maintaining quality procedures. The position requires a bachelor's degree in a relevant scientific discipline, more than five years of quality or manufacturing experience, strong GMP and analytical skills, and advanced English proficiency.
