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NorthStar

The Radiopharmaceutical Manufacturing Associate performs duties to support the development and manufacturing of radiopharmaceuticals for NorthStar operations. This includes equipment preparation, product dissolution, and dispensing of medical radioisotopes while complying with procedures, instructions, and prescribed routines. All duties and responsibilities will be completed in compliance with applicable regulatory agency standards. This position supports production in a 24-hour manufacturing facility which means your schedule provides days off during the week when weekend work is required. Early morning, late evening, weekend, and some holiday work will be required with occasional overtime. Please note requirements include compliance with clean room gowning protocols, which means all jewelry, including physically attached items, must not interfere with the effectiveness of personal protective equipment. In addition, all cosmetics, fragranced products (perfumes, aftershave, etc.), and nail products are prohibited, including clear nail polish, artificial nails, and nail extenders.

The CDMO Product Development Technician II will provide support in NorthStar’s radiologic science laboratories within the CDMO Product Development Department. Responsibilities include the ability to independently perform laboratory controls, maintenance and calibration of equipment, manifestation and disposal of radioactive material, preparation of laboratory solutions, assistance with product development/production, and general laboratory maintenance. This role will specialize in development, verification, and validation of current and/or new and existing radiopharmaceutical products/medical devices. The Senior CDMO Product Development Technician will have additional responsibilities, including leading laboratory process improvements, conducting training for others entering the radiation space, and providing direction and leadership to other technicians.

The Accelerator Operator is responsible for performing routine and non-routine particle (electron) accelerator equipment operations and maintenance tasks necessary to safely, compliantly and efficiently manufacture bulk radiopharmaceuticals. This position will assist with commissioning and installation of systems and equipment, and the development of associated process procedures and instructions. Following this, the role will transition to a traditional role of routine operations and maintenance. The individual will be part of the operational success of the radioisotope production process including accelerator startup/shutdown operations and maintenance, target irradiation, and other routine operations.