Job Overview
The primary objective of this role is to spearhead quality oversight and direction for Sterile Drug Product Filling operations.
* To write, review, and approve Standard Operating Procedures, Work Instructions, Quality Technical Agreements, Master Batch Records, Specifications, and other GMP documentation in line with established policies.
* Engage actively within cross-functional project teams to address issues promptly and provide input on real-time questions.
A high level of initiative, energy, motivation, and excellent organizational skills are expected from the successful candidate. Additionally, they must be able to effectively promote quality across teams.