Nuclear Manufacturing Supervisor

Cardinal Health

About The Position

What Nuclear Manufacturing contributes to Cardinal Health Manufacturing is responsible for cost of production and maintenance activities including process improvement, supply chain management, quality assurance, employee safety and engagement, and environmental commitment. Nuclear Manufacturing is responsible for the manufacturing of time sensitive radiopharmaceuticals in an integrity driven, highly regulated environment (i.e. FDA, NRC, DOT) to support patient treatment through disease diagnosis, staging, and monitoring. Schedule Monday - Friday Overnights/early mornings (can be starting your shift anytime between 8pm - 4am), based on business needs. Schedule can vary but you must be willing to work what is needed based off of business needs which can include some weekends and holidays. Candidate must be flexible to work different shifts, schedules, holidays, days and overtime as needed. 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

Requirements

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 preferred
Strong communication skills
Ability to manage up to 75 pounds
Ability to rotate shifts and/or schedules as business need requires. This will include weekends and holidays responsibilities.

Nice To Haves

Demonstrated experience success at managing a cross functional team preferred
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