This is a Night Shift - 8pm to 6am, 4 days/week Objective As Radiopharmaceutical Production Supervisor you will lead the laboratory procedures and processes involved in the manufacturing process to commercialize investigational drug products. You will be responsible for leading radiochemical synthesis, radiopharmaceutical manufacturing operations, with knowledge of relevant regulations including U.S. FDA 21 CFR 58, laboratory safety, radiation safety, and GMP operations. You will train, mentor, develop, and oversee the production staff in their nightly duties, promoting a culture of continuous improvement in manufacturing procedures. You will be responsible for collaborating with Quality, Facilities, Safety, and other departments to promote cross-functional teamwork and cooperation on action plans/project management. You will possess strong leadership skills, technical experience in a radiopharmaceutical or pharmaceutical manufacturing environment, and a keen understanding of regulatory compliance in the production of radiopharmaceuticals. You will have proven supervisory experience (hiring, training, performance management, staff development) along with excellent production operations and extensive knowledge of quality control ensuring the safe and efficient manufacturing of high-quality radiopharmaceutical products. This is a hands-on role and as production sites and trials expand, there will be opportunities for managerial responsibilities. Essential Functions Supervise Production Operations : Manage the daily operations of the radiopharmaceutical production line during the night shift, ensuring all processes are performed according to standard operating procedures (SOPs), safety guidelines, and regulatory requirements. Maintain accurate record keeping in accordance with GMP. Team Leadership & Development : Lead and mentor a team of production technicians, ensuring effective communication, teamwork, and a positive work environment. Provide training and support to team members on SOPs, GMP standards, and safety protocols. Quality Control & Assurance : Ensure compliance with Good Manufacturing Practices (GMP), cGMP, and all regulatory requirements. Oversee the monitoring of product quality and ensure that all produced radiopharmaceuticals meet the required specifications before release. Production Planning & Scheduling : Collaborate with the production planning team and Senior Production Manager to ensure that production schedules are adhered to, and that resources (materials, equipment, personnel) are appropriately allocated to meet production targets. Troubleshooting & Problem-Solving : Address, resolve and document any production issues that arise during the night shift, including equipment malfunctions, production delays, or quality concerns. Escalate issues when necessary to ensure timely resolution. Safety & Compliance : Ensure all safety protocols, particularly those related to radiation safety, hazardous materials, and equipment operation, are followed. Promote a culture of safety within the team and ensure all team members are trained and compliant with safety regulations. Documentation & Reporting : Maintain accurate and up-to-date records of production activities, including batch records, production logs, quality control documentation, and any incidents or deviations. Report key metrics and production performance to upper management. Continuous Improvement : Actively participate in initiatives to improve production efficiency, reduce waste, and increase output while maintaining the highest quality standards. Provide feedback to the management team on process improvements and operational efficiency. Qualifications Strong leadership and team management skills, with a proven ability to motivate and guide production teams. Excellent problem-solving and troubleshooting abilities, particularly in high-stakes production environments. Proficient in the use of production software and documentation management systems. Strong understanding of safety standards, particularly radiation safety, and hazardous material handling. Excellent communication skills including the ability present data in a comprehensive format to sr. leadership and the ability to work cross-functionally with other departments (e.g., Quality Assurance, Maintenance, Planning). Positive attitude and collaborative spirit needed. Education / Experience A Bachelor's degree in a scientific discipline (e.g., Chemistry, Biochemistry, Biology, Pharmaceutical Sciences) is preferred. Additional certifications in radiopharmaceuticals or GMP are a plus. At least 4-5 years of experience in pharmaceutical or radiopharmaceutical manufacturing, with 3-5 years of production supervision or management. Hands-on experience with radiopharmaceutical production, radiological safety, and GMP-compliant manufacturing processes is highly preferred. Familiarity with regulatory requirements such as FDA, DEA, and cGMP guidelines Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice. Work Environment This is a Night Shift - 8pm to 6am, 4 days/week The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Must be willing to work in a facility producing radioactive materials and requiring all employees to participate in safety programs designed to minimize potential and/or actual exposure levels. Must be able to work outside of regular work hours, (8pm – 6am) including off shift, weekend, and holiday work as business needs require. May be required to sit or stand for long periods of 8 hours a day while performing duties. Occasional kneeling, crouching, twisting the upper body, bending, stooping, pushing, pulling, or reaching may be required. Must possess good hand-eye coordination; close attention to detail is required. Must be able to work indoors and outdoors with exposure to mechanical/moving parts, hazards including radioactive, corrosive, flammable and toxic material, dust, dirt, odors, and irritants. Must be willing to wear a variety of Personal Protective Equipment (PPE), including eye and hearing protection, as needed. Willingness to complete safety training within allotted timeframes, and work in a team-based environment. For information on Perspective Therapeutics, visit our website at: www.perspectivetherapeutics.com. Perspective Therapeutics provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.