Lead QA Operations for Vaccine and Biopharma Manufacturing
In this pivotal role, you will oversee the Quality Assurance (QA) Operations team responsible for ensuring Good Manufacturing Practice (GMP) compliance across a manufacturing site. As Associate Director of QA, you will guide a growing team of specialists in both Drug Substance (DS) and Drug Product (DP) manufacturing.
Main Responsibilities:
* Act as the QA Operations lead for onsite quality monitoring of DS and DP manufacturing
* Support technology transfer, shake down batches, and site GMP readiness initiatives
Requirements:
A successful candidate has:
* A Degree in Biopharmaceutical Science or a related discipline
* Minimum 8 years experience in vaccine or biopharma DS/DP manufacturing, preferably with sterile filling experience
* A proven track record in managing a team, mentoring specialists, and driving operational excellence
Desirable Skills:
Experience in startup or early-stage facility environments, including GMP readiness and inspections, along with strong knowledge of European regulations, cGMP, and quality compliance standards are highly desirable.
What We Offer:
This role requires excellent interpersonal and communication skills to collaborate in a matrix environment.