Associate Director, Stability Lead Development & Clinical

Role: Lead stability strategy for Moderna's mRNA portfolio, supporting development, clinical, and commercial products. Responsibilities: define and execute phase-appropriate stability plans, oversee stability protocols, review data, and author regulatory submissions; collaborate with cross-functional teams including Analytical Development, Quality, Regulatory, and Supply Chain; lead investigations related to stability issues and contribute to lifecycle management; leverage digital tools and analytics to enhance decision-making. Requirements: Bachelor's in Life Sciences, Chemistry, Engineering, or related field with 12+ years of experience or a PhD with 5+ years; strong expertise in stability for biologics, vaccines, or complex drug products; proven experience in regulatory submissions and stability data interpretation. Preferred: advanced degree, leadership in stability for biologics/vaccines, experience with regulatory interactions, and cross-functional influence skills. HighValue: biologics/vaccines, mRNA technology, development and commercial stages, stability and lifecycle management, GxP compliance, and cross-disciplinary team collaboration. WorkSetup: predominantly on-site at Norwood, MA with matrix leadership responsibilities.