Associate Director Quality Assurance (JMR)
Job Location: East Windsor, NJ
Date Posted: 2020-09-15
(Cell/Clinical Contract Manufacturing Compliance Preferred)
Growing Biotechnology Innovator needs someone to manage outsourced contract manufacturing and development organizations (CDMO) to maintain and improve compliance to the company’s quality standards (FDA/EMA). Will perform product release activities including reviewing batch records, analytical test data, and other documentation for product release. Will track and trend deviations, corrective actions, and process data.
Position will require 8+ years in quality assurance preferably with cell/clinical manufacturing compliance experience.
Please contact Joe Raia at email@example.com
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