PET Site Supervisor

Cardinal HealthTampa, FL
23h

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 40 hours per week. The typical schedule is Monday through Friday with a start time anywhere between the hours of 7:00p and 4:00a. for an 8 hour day. Candidate must be flexible to work different days, hours and schedules based on business needs.

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 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

  • Experience with the manufacturing of FDG and Sodium Flouride is preferred
  • Demonstrated project management experience strongly 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

Benefits

  • Cardinal Health offers a wide variety of benefits and programs to support health and well-being.
  • Medical, dental and vision coverage
  • Paid time off plan
  • Health savings account (HSA)
  • 401k savings plan
  • Access to wages before pay day with myFlexPay
  • Flexible spending accounts (FSAs)
  • Short- and long-term disability coverage
  • Work-Life resources
  • Paid parental leave
  • Healthy lifestyle programs
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