PET Site Supervisor

Cardinal Health•Atlanta, GA

6d•$80,900 - $115,500•Onsite

About The Position

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. The primary work environment consists of a cyclotron and associated manufacturing facility to produce PET radiopharmaceuticals, which must be kept clean, orderly, properly lighted and maintained in optimum operating condition. Employees handle radioactive materials and are exposed to very low amounts of radiation that are deemed safe by current standards. The facility is operated under well-controlled and closely monitored conditions that are regulated by both State and Federal agencies, and that are enforced by the corporate internal quality and regulatory group. Each staff member will receive specific training in keeping radiation exposures within regulatory guidelines and he/she will be routinely monitored for their exposure to radiation. Noise levels are considered low to moderate.

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
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

Nice To Haves

Bachelor’s degree in related field, or equivalent work experience preferred
4-8 years of experience preferred
Experience with the manufacturing of FDG and Sodium Fluoride is preferred
Demonstrated project management experience strongly preferred
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