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Quality Control Manager

Job in Carmel, Hamilton County, Indiana, 46033, USA
Listing for: Aegis Worldwide
Full Time position
Listed on 2026-08-08
Job specializations:
  • Quality Assurance - QA/QC
    Regulatory Compliance Specialist, Quality Control - QC Analysts/Managers, Production QC/QA
Salary/Wage Range or Industry Benchmark: 90000 - 130000 USD Yearly USD 90000.00 130000.00 YEAR
Job Description & How to Apply Below

This role ensures timely testing and notification of any abnormal occurrences that could negatively affect manufactured products. The Manager oversees and maintains quality programs to ensure that all test specifications are met for raw materials, components, and validation testing. This position is responsible for scheduling laboratory testing, and implementing corrective actions.

Must Haves:
  • Bachelor's degree in chemistry, science, or related field highly preferred
  • 10+ years of quality control experience in a lab setting
  • 2+ years of experience managing processes or people in a quality control setting
  • Extensive experience with HPLC
Job Responsibilities:
  • Support investigations into product or process failures and customer complaints, author and review quality and safety reports and investigation findings.
  • Drive timely completion of all assigned corrective actions within the area.
  • Ensure safe handling of radioactive materials and maintain team exposure levels in line with As Low As Reasonably Achievable principles.
  • Mentor and develop team members to achieve high performance while promoting accountability and team ownership; recognize and reward strong performance.
  • Establish clear direction by aligning team goals with site strategies and actively managing individual performance.
  • Maintain compliance with U.S. and international regulatory standards and guidelines.
  • Collaborate cross-functionally to coordinate testing schedules and communication, supporting weekly production and ensuring QC testing and maintenance meet requirements.
  • Plan and oversee testing for production samples, raw materials, components, stability studies, validation activities, and experimental/protocol samples.
  • Review, verify, and update controlled documents related to the area of responsibility as needed.
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