Radiopharma Site Supervisor - Nuclear Manufacturing

Cardinal Health, Inc.; Birmingham (AL); On-site; USD 81,000 - 116,000; Full time

Benefits offered by this job

Medical/Dental/Vision

Paid time off

Health savings account

401k savings plan

myFlexPay access

FSAs

Disability coverage

Work-Life resources

Paid parental leave

Healthy lifestyle programs

Job summary

Cardinal Health, Inc. is seeking a Nuclear Manufacturing professional in Birmingham, AL to lead manufacturing operations for time-sensitive radiopharmaceuticals in a regulated environment.

You will manage staff, ensure regulatory compliance, and drive quality and financial reporting in a fast-paced setting. The role requires 4–8 years of experience, strong leadership, and the ability to adapt to varying shifts while maintaining cGMP and GDP standards.

Qualifications

• Bachelor’s degree in related field, or equivalent work experience preferred.
• 4-8 years of experience preferred.
• Ability to obtain and maintain current qualifications to include production and/or quality.
• Demonstrated success in managing people and leading a team.
• Strong communication skills.
• Ability to lift up to 55 lbs.
• Ability to rotate shifts and/or schedules as business need requires. This will include weekends, holidays and on call responsibilities.
• Demonstrated experience success at managing a cross functional team required.
• Experience with the manufacturing of FDG and Sodium Fluoride is preferred.
• Demonstrated project management experience strongly preferred.
• Experience working in compliance with all regulatory standards including Environmental Health and Safety, cGMP, Radiation Safety, applicable FDA and pharmacy laws, DOT, and internal policies and interpretations.
• Past experience conducting performance reviews preferred.
• Past experience creating employee schedules around manufacturing production hours and needs preferred.
• Prior budgeting experience preferred.
• Past financial reporting experience preferred.

Responsibilities

• Works in compliance with all regulatory standards including EHS, cGMP, Radiation Safety, applicable FDA and pharmacy laws, DOT, and internal policies and interpretations
• Manages small group of staff to ensure manufacturing operations
• Conducts performance reviews
• Creates employee schedules around manufacturing production hours and needs
• Handles facility budgeting. Generates reports as it relates to financial performance
• Acts as Project Manager for investigational new drugs
• Executes Standard Operating Procedures (SOPs) in accordance with current Good Manufacturing Practices (cGMP) requirements including Good Documentation Practices (GDP)
• Monitors and verifies quality in accordance with SOPs
• Performs general maintenance
• Maintains a sterile environment, including required cleaning of equipment and facility
• Work in partnership with cross functional teams to ensure product/production expectations and demands are met
• Adheres to a large volume of SOPs, with the ability to adapt to process improvements
• Utilizes technology to support manufacturing processes
• Maintain qualifications for production and/or quality in order to release product

Education

Bachelor’s degree in related field

Job description

Cardinal Health, Inc. is seeking a Nuclear Manufacturing professional in Birmingham, AL to lead manufacturing operations for time-sensitive radiopharmaceuticals in a regulated environment.

You will manage staff, ensure regulatory compliance, and drive quality and financial reporting in a fast-paced setting. The role requires 4–8 years of experience, strong leadership, and the ability to adapt to varying shifts while maintaining cGMP and GDP standards.