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Production Manager, Post Sterilization Services

Job in Ellettsville, Monroe County, Indiana, 47429, USA
Listing for: americas-cookmedical
Full Time position
Listed on 2026-09-06
Job specializations:
  • Manufacturing / Production
    Production Manager, Regulatory Compliance Specialist, Quality Engineering
Salary/Wage Range or Industry Benchmark: 75000 - 105000 USD Yearly USD 75000.00 105000.00 YEAR
Job Description & How to Apply Below
Location: Ellettsville

Overview

The Production Manager at Cook Incorporated establishes directions and goals within one or more manufacturing departments and ensures conformance/compliance to internal procedures and external standards; and ensures adequate resources are available to meet delivery standards for internal and external products. This position interacts regularly with Operations Management to support global business direction & identify areas in need of improvement.

Responsibilities
  • Maintain first-hand understanding of the state of the department(s) by spending an effective amount of time in the department(s)
  • Ensure work order status is updated in a timely manner
  • Maintain and evaluate KPI’s for productivity and evaluations
  • Recognize, develop and utilize natural leaders
  • Must be heavily involved with all personnel matters including employee performance issues, corrective action processes, and employee development plans and actions
  • Drive quality and efficiency improvements
  • Provide direction/guidance to ensure that expectations and goals are clear and understood
  • Ensure work is being completed in a safe, sanitary and orderly environment
  • Ensure area functions effectively independent of leadership oversight
  • Support audits, investigations and tours within the department
  • Ensure compliance of, and adherence to, internal procedures and processes
  • Initiate actions to improve quality and efficiency
  • Must maintain all training requirements for the position, while seeking out opportunities for continuous development and growth
  • Adhere to the Quality Management System and its processes to meet FDA 21 CFR 820, ISO 13485, and other applicable regulatory requirements
Qualifications
  • High School Diploma or GED required
  • Bachelors degree in Engineering, Management or a related field; or experience of such kind and amount as to provide a comparable background preferred
  • Minimum 2 years experience in manufacturing management preferred
  • Knowledge of/or training in ISO, GMP and CFR standards
  • Computer proficiency, experience with Microsoft products (Word and Excel)
Physical Requirements:
  • General office setting.
  • Exposure to moderate noise and light levels within manufacturing facility
  • Requires close visual acuity when working with computers, etc.
  • Maintain a physical presence in the area of responsibility
  • Proper attire/clothing and personal protective equipment/clothing as required within Controlled Production Areas
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