Temp Regulatory Document Associate
Regeneron Pharmaceuticals, Inc.
Position Description Regulatory Document Associate for the department will review draft pharmaceutical regulatory documents to ensure the accuracy and consistency of data and other content included in regulatory submissions and related documents. The Regulatory Document Associate will review content primarily related to biopharmaceutical chemistry, manufacturing, and controls. Additional opportunities may arise for a Regulatory Document Associate with copyediting experience. Regulatory Document Associate - R45236 Roles Responsibilities Locate appropriate source documents and perform data verification Verify consistency of data and content included in multiple sections of submission documents Maintain consistent terminology, names, and abbreviations Skills Rigorous attention to detail, exceptional organizational and communication skills Comfort with technical/scientific content and with navigating multiple systems, and the ability to work well under tight deadlines. Education Requires a four-year degree in related field Previous experience with detailed document review is strongly preferred. Experience with or knowledge of biopharmaceutical development, testing, or manufacturing a plus. #J-18808-Ljbffr Regeneron
Vacancy posted 5 days ago
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