Director, CMC Technical Program Management

Role: Senior CMC Program Leader coordinating radiopharmaceutical development, manufacturing, and regulatory activities within Perspective Therapeutics. Responsibilities: develop and execute integrated plans across CMC, manufacturing, Quality, Regulatory, and Supply Chain functions; lead technology transfer and risk management; support regulatory submissions (INDs, NDA/BLA); partner with cross-functional teams to ensure clinical supply continuity; maintain project plans and drive program milestones from early development through commercialization. Requirements: advanced degree (M.S., Ph.D., Pharm.D.) in pharmaceutical sciences or related field; 10+ years in pharma/biotech with extensive experience leading cross-functional CMC initiatives; strong understanding of radiopharmaceutical, biologics, or complex therapies, GMP manufacturing, and regulatory standards (FDA, EMA, ICH); proficiency in project management tools. Preferred: experience with radiopharmaceuticals, biologics, or gene therapies, and contribution to regulatory filings. High-Value: radiopharmaceutical development, CMC, technology transfer, regulatory submissions, cross-functional leadership, 30% travel possible. WorkSetup: not specified.