Provide Quality assistance and oversight during manufacturing of in-process, upstream and downstream, and other GMP processes as required. Assists in the identification, generation and quality approval of investigation records that may result during day-to-day operations. Assure the quality of manufactured products complies with all applicable regulations and guidelines.
· BS/BA in Biological Sciences or equivalent relevant career experience.
· 3 + years of experience in a Pharmaceuticals environment.
· Practice knowledge and understanding of cGMPs.