Radiopharmaceutical Manufacturing Associate (3rd Shift)

NorthStar Medical Radioisotopes, LLC; Beloit (WI); On-site; USD 45,000 - 60,000; Full time

Benefits offered by this job

Competitive benefits package

World-class facilities

Job summary

A leading radiopharmaceutical company in Beloit is seeking a Radiopharmaceutical Manufacturing Associate for the 3rd shift. This entry-level full-time position involves executing manufacturing processes, maintaining safety checks, managing inventory, and ensuring cleanliness in production areas. Candidates with an Associate’s Degree in a STEM discipline and a passion for pharmaceutical manufacturing are encouraged to apply. The company offers a competitive benefits package and focuses on innovative therapies for cancer care.

Qualifications

• Associate’s Degree (AS) in a STEM discipline or equivalent.
• Bachelor's Degree in a STEM discipline and minimum one year of cGMP experience preferred.

Responsibilities

• Execute various aspects of radiopharmaceutical manufacturing.
• Assist in preparation and completion of manufacturing records.
• Perform safety checks and inspect processing equipment.
• Maintain cleanliness and orderliness of manufacturing spaces.
• Support troubleshooting of manufacturing equipment and process issues.

Skills

Manufacturing processes

Record keeping

Safety checks

Inventory tracking

Troubleshooting

Education

Associate’s Degree in STEM

Bachelor's Degree in STEM

Job description

Radiopharmaceutical Manufacturing Associate (3rd Shift)

Join the best radiopharmaceutical company in the world. NorthStar 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 cleanrooms 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 NorthStar 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.