Provide end‑to‑end quality oversight across manufacturing, testing, documentation, and product disposition
Job Summary
Provide end‑to‑end quality oversight across manufacturing, testing, documentation, and product disposition.
You’ll be a key partner to Operations, QC, Engineering, Supply Chain and QPs, helping maintain a robust Quality Management System and supporting inspection readiness across the site.
Play a pivotal role in safeguarding the quality of life‑changing biologic medicines, where your expertise directly protects patients and strengthens a world‑class manufacturing site.
Matching Summary
Provide end‑to‑end quality oversight across manufacturing, testing, documentation, and product disposition.
Skills & Requirements
Must-have
cGMP oversight
batch record review and approval
technical documentation review
QMS elements oversight
health authority inspection engagement
Nice-to-have
thrive in fast-paced environment
meaningful difference
inclusive and equitable environment
Key Requirements
Degree in Pharmacy, Biology, Biotechnology, Engineering, or relevant scientific discipline
Fluency in written and spoken English
Experience in pharmaceutical or biotech industry
Solid understanding of GMP, quality systems, and regulatory expectations