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Aegis Worldwide

Quality Control Manager

carmel, IN

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About this opportunity

Aegis Worldwide lists this Quality Control Manager opportunity in carmel, Indiana. Review the employer’s description below for duties, qualifications and application requirements.

Job description

Aegis Worldwide

Quality Control Supervisor

3rd Shift

$115,000 - 135,000

Position Summary:

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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