Supervisor, Radiopharmaceutical Manufacturing

NorthStar Medical Technologies; Beloit (WI); On-site; USD 65,000 - 90,000; Full time

Job summary

NorthStar Medical Radioisotopes seeks a motivated manufacturing leader to oversee day-to-day operations in radiopharmaceutical production and ensure regulatory compliance. You will lead a team, drive training, and maintain quality standards across the line.

The role requires an AS in a STEM field with 4+ years of cGMP experience and at least 1 year of leadership. The company emphasizes growth, safety, and reliability in a fast-growing field.

Qualifications

• Associate’s Degree in STEM with 4+ years cGMP experience; 1+ year leading others required.

Responsibilities

• Manage day-to-day activities and personnel to ensure compliant manufacturing and meeting master production schedules.
• Provide leadership, training, and support to the team.
• Monitor and enforce strict quality assurance procedures and key operational metrics.

Skills

Leadership

Team management

Regulatory compliance

Quality assurance

Education

Associate’s Degree 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.

• Manage the day-to-day activities and personnel to ensure efficient manufacturing of products to meet the master production schedule ensuring compliance with regulatory requirements, while maintaining high safety standards.
• Provide leadership, training, and support to the team. Responsible for the performance of team members and ensuring training requirements are achieved.
• Monitor and enforce strict quality assurance procedures and key operational metrics to meet the specifications of each product.
• Address and resolve any issues related to equipment, processes, or personnel in a timely and effective manner with proper communication and/or escalation as needed.
• Effectively communicate with essential manufacturing support groups to ensure clarity on product specifications, address any escalations promptly, and coordinate delivery schedules. Regularly update management on production status and any critical issues.
• Responsible to ensure complete and accurate records are maintained for Radiopharmaceutical Manufacturing (Batch Production Record) according to customer and/or Product Development orders.
• Assist leader in maintaining the department’s budget, focusing on the efficient allocation and utilization of resources by monitoring monthly production expenditures.
• Collaborate with the manufacturing support teams to allocate resources effectively, supporting the technology transfer and process scale-ups in radiopharmaceutical manufacturing to meet business needs and product development goals.

Associate’s Degree (AS) in a STEM discipline and minimum four (4) years of cGMP experience; or equivalent combination of education and experience. Minimum one (1) year of experience leading others 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.