Manager, QA - Drug Product (Parenteral)

Company: Bristol Myers Squibb

Job Description

Responsible for reviewing and approving batch and test documentation for investigational medicinal products, APIs, raw materials, and packaging components, ensuring compliance with GMP regulations and releasing compliant materials. Supports investigations of non-conformances and quality incidents, and reviews/approves Quality System documents like batch records and validation protocols.

Requirements

• MS with 4-6 years or BS with 7-9 years of pharmaceutical/healthcare experience, including 2-4 years in a regulated function.
• Strong knowledge of GMP, pharmaceutical processing, and leadership skills are essential.