Associate Director, CMC Regulatory Affairs – Small Molecules

Monte Rosa Therapeutics, Inc is seeking an Associate Director of CMC Regulatory Affairs to lead global regulatory strategies for Chemistry, Manufacturing, and Controls across development stages. You will author Module 3 content, review summaries, and partner with Process Chemistry, Analytical Development, Drug Product, Quality, and Clinical Supply teams to ensure compliant filings.The ideal candidate has 8+ years in CMC regulatory affairs, experience with IND/CTA submissions and NDA/MAA/BLA, #J-18808-Ljbffr