Description
The Manager, Quality Systems leads the development, implementation, and continuous improvement of pharmaceutical quality systems, including change control, deviations, investigations, CAPA, document and record management, training, quality metrics, management reviews, internal audits, regulatory inspections, and quality complaint investigations. The role manages audit and regulatory inspection responses, supports regulatory submissions, coordinates with third parties and regulatory agencies, and may support QA operations, product release, and stability oversight. It is an on-site Monday-through-Friday position requiring a bachelor’s degree, at least eight years of experience in the pharmaceutical, medical device, vaccines, blood, or biologics industry, and at least five years of quality assurance experience with quality systems responsibilities.
