Description
This pharmaceutical Quality Assurance role manages workflows within and across quality functions, resolves cross-functional events, approves standards and products, oversees testing and GMP compliance, evaluates manufacturing and control records, and supervises direct reports. The position requires extensive US and European drug-product GMP knowledge, pharmaceutical quality assurance experience, technology-transfer and facility-qualification experience, a bachelor’s degree in a scientific discipline, and at least eight years of pharmaceutical quality assurance experience, preferably with parenteral dosage forms. It is an onsite position.
