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Posted 2/07/2018

AustarPharma LLC  in Edison, NJ is seeking a Regulatory Affairs Specialist:  MS in  Pharmaceutics , Pharmaceutical Chemistry or closely related fields with at least 1 year of experience in  collecting and reviewing technical CMC documents,  reviewing clinical study protocols and reports, and providing guidance to ANDA R&D departments for FDA and cGMP complianceExperience in drug development with solid dosage form, drug analysis, drug delivery and clinical trial design is also required.  Send resume to: Ms. Ivy Lee  at

Post expires 3/09/2018

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