Description
Aquestive is hiring two Manufacturing Quality Associates to support GMP and quality compliance across development and commercial manufacturing. The role monitors manufacturing operations, conducts audits and walkthroughs, investigates nonconformances and product complaints, manages CAPA records, supports environmental monitoring and quality projects, reviews batch and operational records, performs AQL testing and line clearances, and maintains quality documentation. The positions are available on the 2nd shift from 12:00 PM to 8:30 PM and the 3rd shift from 12:00 AM to 8:30 AM, with off-hours and weekend work as needed. A bachelor's degree is required, preferably in chemistry, biochemistry, or a related science field, and at least five years of related experience in the pharmaceutical, biotechnology, or medical device industry is preferred.
