Schedule

• Monday - Friday

• Overnights/early mornings

• 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

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 preferred

• Strong communication skills

• Ability to manage weight up to 75 pounds

• Ability to rotate shifts and/or schedules as business need requires.  This could include weekends and holidays.

• 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

What is expected of you and others at this level

• Coordinates and supervises the daily activities of operations or business staff

• Administers and exercises policies and procedures

• Ensures employees operate within guidelines

• Decisions have a direct impact to work unit operations and customers

• Frequently interacts with subordinates, customers, and peer groups at various management levels

• Interactions normally involve information exchange and basic problem resolution

Anticipated salary range: $80,900 - $115,500

Bonus eligible: Yes

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

Application window anticipated to close: 1/26/2026 *if interested in opportunity, please submit application as soon as possible.

The salary range listed is an estimate. Pay at Cardinal Health is determined by multiple factors including, but not limited to, a candidate?s geographical location, relevant education, experience and skills and an evaluation of internal pay equity.