Global MSAT Drug Product Qualification and Validation Lead
KI-Beschreibung
In this role, you will lead the global strategy for drug product manufacturing processes, ensuring compliance and quality through equipment qualification and validation. Your expertise will guide teams in implementing best practices and navigating regulatory inspections.
Anforderungen
ca. 4 – 6 Jahre- •Ph.D. in pharmaceutical sciences, engineering, biochemistry, or related field, or equivalent experience
- •Expertise in equipment qualification for aseptic drug product manufacturing
- •Extensive experience in process validation for sterile biologics, including lyophilized and liquid formats