MMS Holdings Inc. is seeking a regulatory writer focused on nonclinical documents for UK-based remote work. You will develop and manage technical submissions (Module 2.4/2.6, IB, NCSRs, RTQs) and ensure compliance with GLP, ICH, FDA/EMA guidelines. Lead projects, collaborate with cross-functional teams, and guide junior writers to deliver high-quality regulatory content in alignment with sponsor formats and timelines. #J-18808-Ljbffr
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