Quality Supervisor - 3rd shift

The Quality Supervisor – 3rd Shift will be responsible for overseeing quality personnel, processes, and compliance within an assigned production area. The ideal candidate will support continuous improvement initiatives, drive adherence to quality standards, and provide strong leadership through coaching, goal-setting, and effective communication. This role plays a key part in ensuring product quality and regulatory compliance in a high-performance medical device environment.

Key Responsibilities:

• Coordinate and supervise inspection activities based on production priorities, resource availability, and inspector training levels.

• Support and schedule inspections and special testing required for product release, validation builds, or non-conforming materials.

• Communicate personnel, process, material, and compliance issues to the QC Manager in a timely manner.

• Lead and coordinate inventory inspections for non-conforming components that may impact compliance with product specifications.

• Investigate corrective action requests (CARs) and drive root cause analysis, identification of solutions, and implementation of corrective actions.

• Review and ensure proper completion of all required quality records and documentation for product and process inspections.

• Ensure product and process compliance with internal procedures, industry standards, and customer quality requirements.

• Provide ongoing training and development to quality inspectors regarding procedures, standards, and quality expectations.

• Support ISO and quality system activities, maintaining alignment with regulatory requirements.