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Supervisor, Production Management

Job in Aurora, Arapahoe County, Colorado, 80012, USA
Listing for: Cardinal Health
Full Time position
Listed on 2025-12-18
Job specializations:
  • Manufacturing / Production
    Production Manager, Operations Manager
Salary/Wage Range or Industry Benchmark: 75600 - 107900 USD Yearly USD 75600.00 107900.00 YEAR
Job Description & How to Apply Below
Supervisor, Production Management page is loaded## Supervisor, Production Management locations:
CO-Aurora-Nuclear Manuf Svcstime type:
Full time posted on:
Posted Todayjob requisition :

** Anticipated salary range:**$75,600 - $107,900
** Bonus eligible:
** No
* * 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 myFlex Pay
* Flexible spending accounts (FSAs)
* Short- and long-term disability coverage
* Work-Life resources
* Paid parental leave
* Healthy lifestyle programs
** Application window anticipated to close:
** 12/28/2025  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.
*** What Production Management contributes to Cardinal Health
*** Responsible for Production Operations, Maintenance, Plant Engineering, Safety, Quality Control, Scheduling, Accounting, and Employees. Supervises plant personnel directly and through subordinate managers and/or supervisors. Prepares and maintains long- and short-range plans. Promotes good relations with community, government agencies, customers, and union representatives. Conduct or participates in conduct of labor negotiations and administers wage, salary, and bonus programs in accordance with corporate policies.

Reviews, evaluates, and approves promotion and transfer of exempt personnel
*** Shift/Schedule
**** Day Shift Supervisor
* 10 Hour Shifts
* Saturday – Tuesday 9:30am - 8:00pm
* Candidate must be flexible to work different days, schedule or hours based on business need.
*** Responsibilities
* *** Handles planning and implementation of I-123 Iodine capsules in a pharmaceutical manufacturing cGMP production environment.
* Communicate activities to the manufacturing team to meet assigned manufacturing goals; directs the work activities of manufacturing technicians including shift assignments, safety, cGMP compliance and training programs.
* Participates with other manufacturing management staff in the planning and implementation of work schedules, equipment and materials needs, and staffing requirements to meet safety, quality, and productivity goals.
* Ensures efficient use of human resources by regularly monitoring work activities, setting performance expectations and measuring results, and providing feedback to employees daily.
* Formulates and recommends manufacturing policies, procedures and programs that enhance overall effectiveness of the operating unit.
* Ensures that required training for specific work activities are completed for all shift staff; maintain up-to-date training records.
* Tracks and reports on manufacturing job duties such as safety incidents, quality issues and throughput measures.
* Set expectations for communications between supporting departments and among manufacturing technicians to facilitate continuous productivity.
* Assists in troubleshooting and problem-solving when process or people problems arise; ensure timely resolution.
* Focus on high safety performance, high quality performance, and high productivity performance.
* Conducts 1 On 1 check points with each tech on your team. Handles performance discussions and writing at the necessary times through the year. This would include but not limited to Our Time To Talk (OTTT ) discussions #1,2,3 and year end.
* Manages time sheets to be completed accurately, ability to coordinate all time off requests.
* Other duties as assigned
*** Qualifications
* *** 4-8 years of experience, preferred
* Bachelor’s degree in related field, or equivalent work experience, preferred
* A minimum of 2+ years related work experience (GMP pharmaceutical or chemical processing experience) preferred
* Strong organizational and planning skills
* Strong interpersonal skills with subordinates as well as peers and superiors
* Excellent understanding of basic…
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