Regulatory Affairs Specialist: GMP, FDA & Compliance
Sunrise Pharmaceutical
A leading pharmaceutical company in New Jersey is seeking a qualified individual to lead compliance efforts related to FDA regulations and GMP standards. The role involves managing documentation, overseeing analytical testing, and ensuring regulatory adherence across production processes. Ideal candidates will hold a Master’s Degree in Pharmaceutical Sciences and have substantial experience in the field. #J-18808-Ljbffr
Vacancy posted 1 day ago
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