The Digital Marketing Intern will be a motivated and organized individual who will assist in enhancing our digital presence and contribute to the company’s growth by building brand awareness both internally and externally.

This position will shepherd Contract Development and Manufacturing Organization (CDMO) projects through their life cycle at NorthStar, including initial kickoff, technology transfer, validation, and drug product manufacturing, both clinical and commercial. The CDMO Project Manager is responsible for providing internal and external leadership for CDMO projects. This role will serve as the main contact for driving the tactical execution of CDMO projects upon contract approvals. This role may also provide support to the Commercial organization in the outreach and courting of new sponsors.

The role of the Senior Regulatory Affairs Specialist is to manage regulatory, quality, and business issues to permit NorthStar to develop, produce, and distribute medical radioisotopes and radiopharmaceuticals that comply with U.S. Food and Drug Administration (FDA) and other applicable requirements.  The Senior Regulatory Affairs Specialist will have primary responsibility to handle day-to-day activities related to FDA electronic submissions for drug marketing approvals. This role will also work with the Vice President, Quality and Regulatory to develop NorthStar regulatory and quality strategy.  

The Senior MS&T, Accelerator Support is responsible for overseeing routine maintenance and repair activities for our particle (electron) accelerators and their supporting systems/equipment; this includes planning, organizing, leading, training, and/or executing maintenance and repair on these systems. This position will also support the commissioning and installation of accelerators and supporting systems/equipment, as well as the development of procedures for associated maintenance and troubleshooting.This position must actively manage these activities with limited...

Design or plan protocols for equipment or processes to produce products meeting internal and external purity, safety, and quality requirements. Establish Commissioning and Qualification (C&Q) policies/strategies, lead specific C&Q projects for radioactive pharmaceutical manufacturing equipment and processes and ensuring compliance with quality standards/requirements and industry standards (FDA, EMA, ISO, ICH, etc.). Drive C&Q project completion and compliance in a challenging and fast-moving environment in a timely and efficient manner. All projects and duties will be completed in compliance with applicable cGMP, FDA, and all other regulatory agencies standards. Effectively...

The Health Physics Technician (HPT) performs technical functions related to NorthStar’s radiation safety program under the supervision of the Lead Health Physicist. The HPT work practices must comply with WI and Federal regulations, NorthStar radioactive material licenses and radiation device registrations, and NorthStar policies and procedures.

The Senior MS&T Engineer is responsible for successful internal and external manufacturing and technical transfer and operational readiness. This includes leading the development and execution of operations and maintenance procedures and other necessary documentation to ensure effective process transfer between process development and operations.   The Senior MS&T Engineer is responsible for leading the development and evaluation of manufacturing processes and implementing equipment and tools for...

The Nuclear Pharmacist will handle radioactive materials within the scope of manufacturing and production of radiopharmaceuticals for clinical trials and commercial products. It is expected that this role will act as the subject matter expert (SME) for radiopharmaceutical preparations, and as such, will participate in routine operations and train operations staff accordingly. This includes equipment calibration, batch dissolution, product synthesis, dispensing of medical radioisotopes, and aliquoting of finished patient doses, while complying with procedures, instructions, and prescribed routines. The Nuclear Pharmacist will draw from experience and expertise to identify and...

The Chemical Process Engineer II will assist the product and process development teams with creation and implementation of simple to complex manufacturing process designs in compliance with cGMP regulations. This position will be responsible for defining and creating new procedures for documenting or qualifying equipment/processing which can be transitioned to manufacturing production engineering team members.  The successful candidate will be familiar with manufacturing within a regulated industry such as medical device/pharmaceutical and possess in-depth engineering knowledge in science.  

The MS&T Engineer is responsible for supporting both internal and external manufacturing and technical transfer activities to support manufacturing readiness. This includes assisting in the development of operations and maintenance procedures and other necessary documentation to ensure effective process transfer between process development and operations.   The MS&T Engineer is responsible for developing and evaluating manufacturing processes and...

The primary role of this position is to conduct and validate various biological and analytical quality control assays associated with the processing of radiopharmaceutical isotopes and drugs to ensure compliance with established standards.   This role requires extensive training on radiation safety including ALARA (“as low as reasonably achievable”) principles.     The Senior Quality Control Analyst will lead various activities, as further described below.    

The Radiopharmaceutical Manufacturing Specialist 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...