Global Radiopharma Supply Chain Manager

Actinium Pharmaceuticals, Inc.; New York (NY); On-site; USD 110,000 - 150,000; Full time

Job summary

Actinium Pharmaceuticals is seeking a Supply Chain Manager to oversee end-to-end logistics for radiopharmaceutical development and clinical trials. You will manage procurement, inventory, and cross-border shipments of materials, isotopes, and patient doses, ensuring GMP/GCP compliance and proper regulatory documentation.

The role requires experience in biotech/pharma supply processes, strong cross-functional collaboration, and the ability to coordinate globally with sites, manufacturers,

Qualifications

• Bachelor’s degree in supply chain, life sciences, or related field.
• 3–5 years of relevant experience in biotech, pharma, or radiopharmaceuticals.
• Familiarity with drug development supply processes, import/export regulations, and radioactive material shipping (preferred).
• Experience with GMP/GCP compliance, SOP development, and inventory management systems is required.
• Specializes in radiopharmaceuticals, isotope logistics, and regulatory compliance for controlled materials.

Responsibilities

• Manage procurement, inventory, and cross-border shipments of materials, isotopes, and patient doses.
• Coordinate import/export documentation.
• Maintain supply chain accuracy.
• Manage vendor relationships.
• Develop SOPs for shipment processes.
• Coordinate global activities with clinical sites, manufacturing, vendors, and regulatory bodies.

Skills

Cross-functional collaboration

GMP/GCP compliance

Inventory management

Logistics management

Regulatory compliance

Education

Bachelor’s degree in supply chain, life sciences, or related field

Tools

Inventory management software

Regulatory documentation systems

Job description

Actinium Pharmaceuticals is seeking a Supply Chain Manager to oversee end-to-end logistics for radiopharmaceutical development and clinical trials. You will manage procurement, inventory, and cross-border shipments of materials, isotopes, and patient doses, ensuring GMP/GCP compliance and proper regulatory documentation.

The role requires experience in biotech/pharma supply processes, strong cross-functional collaboration, and the ability to coordinate globally with sites, manufacturers,