Radiopharmaceutical Manufacturing Specialist (2nd shift)

NorthStar Medical Technologies; Beloit (WI); On-site; USD 60,000 - 110,000; Full time

Job summary

NorthStar Medical Radioisotopes in Beloit, WI seeks a manufacturing associate to execute cGMP-driven radiopharmaceutical production tasks, prepare batch records, review work orders, and maintain cleanroom safety and traceability.

AS or BS in STEM with 2+ years of cGMP experience is required; BS preferred. This role supports process improvement, operates under QMS guidelines, and involves cross-functional collaboration in a fast-growing field.

Qualifications

• AS or BS in STEM with 2+ years of cGMP or related experience.
• Experience producing or supporting radiopharmaceuticals or pharmaceutical manufacturing.
• Experience with batch records, SOPs, WI, and QMS documentation; immigration sponsorship not provided.

Responsibilities

• Execute various aspects of radiopharmaceutical manufacturing including pre-production setup and post-production activities.
• Review production work orders and maintain accurate batch records and logs.
• Perform safety checks, maintain cleanrooms, and ensure equipment traceability.
• Assist in root cause analysis and participate in process improvement projects.

Skills

cGMP knowledge

Record keeping

Cross-functional teamwork

Process improvement

Manufacturing operations

Education

AS in STEM

BS in STEM

Job description

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.

• Execute various aspects of radiopharmaceutical manufacturing, including pre-production set-up, manufacturing processes, post-production activities, and waste stream management.
• Assist in the accurate and timely preparation and completion of records manufacturing, including Batch Records, Forms, Logbooks, etc.
• Review production Work Orders on the production schedule.
• Author, review, and revise cGMP documentations, such as Batch Production Records (BPR), Standard Operating Procedures (SOP), Works Instructions (WI), and Production Checklists while upholding NorthStar’s QMS guidelines.
• Perform safety checks and routine inspection of the production processing equipment and control systems, consumables, and cleanrooms to ensure compliant manufacturing. Notify leader of equipment or operating problems and the need for additional materials, supplies, or investigations.
• Maintain accurate inventory of materials and consumables, and coordinate equipment traceability under the direction of the leader.
• Perform and assist in maintaining the cleanliness and orderliness of the cleanroom and/or manufacturing spaces, equipment, and materials in accordance with NorthStar’s respective policies and procedures.
• Work cross-functionally on employing standardized root cause analysis, investigation tools and methodologies.
• Contribute to interdepartmental projects including production scale-up and continuous process improvement.

Associate’s Degree (AS) in a STEM discipline and minimum two (2) years of cGMP (pharmaceutical or medical device), ISO 15189 (hospital), CLIA (clinical laboratory), ISO 9001 (industrial manufacturing), IATF 16949 (automotive) or AS9100 (aerospace) experience; or equivalent combination of education and experience. Relevant military experience will also be considered.

Bachelor’s Degree (BS) in a STEM discipline and minimum two (2) years of cGMP (pharmaceutical or medical device), ISO 15189 (hospital), CLIA (clinical laboratory), ISO 9001 (industrial manufacturing), IATF 16949 (automotive) or AS9100 (aerospace) experience preferred. CDMO/CMO experience, chemistry experience and knowledge of aseptic processes (cleanroom environment) and equipment qualification preferred.

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.