Senior CMC Regulatory Strategist – Small Molecules

Monte Rosa Therapeutics seeks a seasoned Associate Director of CMC Regulatory Affairs to shape global CMC strategy and author critical submission content. You will collaborate with Process Chemistry, Analytical Development, Drug Product, Quality, and Clinical Supply to ensure compliant, high-quality filings.You will drive Module 3 content, quality summaries, and responses while engaging with FDA/EMA and other regulators. #J-18808-Ljbffr