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Radiopharmaceutical Manufacturing Associate; 3rd Shift

Job in Beloit, Rock County, Wisconsin, 53511, USA
Listing for: NorthStar Medical Radioisotopes, LLC
Full Time position
Listed on 2025-12-07
Job specializations:
  • Manufacturing / Production
    Pharmaceutical Manufacturing, Validation Engineer
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below
Position: Radiopharmaceutical Manufacturing Associate (3rd Shift)

Radiopharmaceutical Manufacturing Associate (3rd Shift)

Join the best radiopharmaceutical company in the world. North Star Medical Radioisotopes offers opportunities in a specialized, fast‑growing field focused on therapeutic radioisotopes and novel radiopharmaceuticals for cancer care.

Responsibilities
  • Execute various aspects of radiopharmaceutical manufacturing, including pre‑production set‑up, manufacturing processes, and post‑production activities.
  • Assist in the accurate and timely preparation and completion of records related to manufacturing, including Batch Records, Forms, Log Books, etc.
  • Perform safety checks and routine inspection of processing equipment, consumables, and clean rooms to ensure effective production. Notify leader of equipment or operating problems and the need for additional materials, supplies, or investigations.
  • Receive and track inventory of materials, consumables, and equipment list and report any deficiencies to the leader.
  • Maintain the cleanliness and orderliness of the cleanroom and/or manufacturing spaces, equipment, and materials in accordance with North Star policies and procedures.
  • Support troubleshooting of manufacturing equipment and process issues, and escalating manufacturing, safety, and compliance issues.
  • Support interdepartmental activities including production scale‑up and continuous process improvement.
Qualifications

Associate’s Degree (AS) in a STEM discipline or equivalent combination of education and experience.

Bachelor's Degree in a STEM discipline and minimum one year (1) of cGMP experience 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.

Seniority Level

Entry level

Employment Type

Full‑time

Job Function & Industries

Research, Analyst, and Information Technology;
Pharmaceutical Manufacturing

Benefits

Competitive benefits package supported by world‑class facilities.

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Position Requirements
10+ Years work experience
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