Nuclear Manufacturing Supervisor

Cardinal Health

83d • $80,900 - $121,275

About The Position

Nuclear Manufacturing contributes to Cardinal Health Manufacturing by being 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. The schedule is Monday - Friday with overnights/early mornings. The schedule can vary, but candidates must be willing to work based on business needs, including different shifts, schedules, holidays, and overtime as needed.

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 manage weight up to 75 pounds.
• Ability to rotate shifts and/or schedules as business need requires, including weekends.
• 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 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 a 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.
• Works 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.
• Maintains qualifications for production and/or quality in order to release product.

Benefits

• 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.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: Bachelor's degree
• Number of Employees: 5,001-10,000 employees