Radiopharma CMC Director: Technical Program Leader

Perspective Therapeutics; United States; Remote; USD 180,000 - 280,000; Full time

Job summary

Perspective Therapeutics seeks a Director of CMC Technical Program Management to lead cross-functional CMC programs from early development through commercialization, with focus on Pb-212 manufacturing, regulatory commitments, and technology transfer.

You will build integrated plans, manage cross-functional deliverables, track milestones, and drive risk mitigation while partnering with Regulatory, Quality, Manufacturing, supply chain, and clinical operations to ensure uninterrupted development

Qualifications

• Advanced degree in pharmaceutical sciences or related life sciences.
• Minimum 10 years in pharma/biotech with cross-functional leadership.
• Experience with regulatory submissions and CMC documentation.
• Experience with radiopharmaceuticals and technology transfer preferred.
• Ability to translate regulatory requirements into execution plans.

Responsibilities

• Lead senior CMC program planning across development to commercialization.
• Translate objectives into integrated execution plans with milestones.
• Coordinate regulatory submissions and manufacturing readiness deliverables.
• Manage technology transfer with CMOs/CDMOs and risk mitigation.
• Develop and maintain CMC risk management and dashboards.
• Partner with Regulatory, Quality, Manufacturing, Supply Chain, and Clinical Ops.

Skills

CMC program leadership

Cross-functional collaboration

Regulatory submissions

Technology transfer

Risk management

Education

Advanced degree in pharmaceutical sciences or related field

Tools

MS Project

Excel

SharePoint

PowerPoint

Job description

Perspective Therapeutics seeks a Director of CMC Technical Program Management to lead cross-functional CMC programs from early development through commercialization, with focus on Pb-212 manufacturing, regulatory commitments, and technology transfer.

You will build integrated plans, manage cross-functional deliverables, track milestones, and drive risk mitigation while partnering with Regulatory, Quality, Manufacturing, supply chain, and clinical operations to ensure uninterrupted development