The role involves leading and managing new parenteral product and process technology transfer projects alongside commercialization efforts
Job Summary
The role involves leading and managing new parenteral product and process technology transfer projects alongside commercialization efforts.
Candidates must possess at least three years of relevant experience in a cGMP parenteral manufacturing site to ensure compliance with safety and quality standards.
The position requires supporting the TS/MS primary loop and production operations while preparing technical documents such as validation protocols and change controls.
Matching Summary
The role involves leading and managing new parenteral product and process technology transfer projects alongside commercialization efforts.