What are the responsibilities and job description for the CDMO Product Development Technician I position at NorthStar Medical Radioisotopes, LLC?
Join the best radiopharmaceutical company in the world!
If you’re looking to make an impact while building a meaningful career in a specialized, fast-growing field, NorthStar Medical Radioisotopes is the place to do it. NorthStar Medical Radioisotopes is a growing, commercial-stage company focused on advancing patient care by providing therapeutic radioisotopes and novel radiopharmaceuticals to detect and treat cancer.
At the forefront of NorthStar’s technological innovation is scientific excellence, using first-in-kind electron accelerator technology and integrated campus capabilities to drive progress in radiopharmaceutical manufacturing. Our work is driven by a meaningful mission—advancing life-saving radiopharmaceutical development and ensuring a reliable supply of critical medical isotopes for patients in need. As a rapidly growing organization operating on the cutting edge of science, we offer exceptional career growth and professional development opportunities, supported by world-class facilities and a competitive benefits package.
- Perform routine and non-routine experiments and/or analyses following NorthStar procedures and guidelines. Ensure data is collected and documented according to good documentation practices.
- With appropriate supervision, perform tasks as needed to support product development. This may include solution preparation, equipment checks, and documentation preparation.
- Perform tasks as needed to support product development. This may include solution preparation, equipment checks, and documentation preparation.
- Understand and execute the cradle-to-grave processes specific to all radioactive substances that are used in the laboratory including, but not limited, to DOT check in/check out process, waste management, and documentation/filing.
- Maintain low-level radioactive waste inventory management including: storage, manifestation, and disposal in accordance with regulatory requirements.
- Maintain supplies and manage inventory within the laboratory space.
Knowledge of ALARA principles required. Previous experience in a nuclear pharmacy, nuclear medicine department, laboratory setting, or cGMP environment preferred.
CDMO Product Development Technician I
Associate’s degree in a related science discipline or related medical field or completion of an accredited Nuclear Medicine Technology educational program required
Please note the company cannot provide immigration-related sponsorship (including H-1B status, O-1 status, Optional Practical Training support, etc.) for this position. Each successful applicant will be required to complete the Form I-9, Employment Eligibility Verification, demonstrating both identity and employment authorization, on or before the first day of employment. Under federal law, only truthful information may be provided on the Form I-9.