Quality Supervisor – Medical Device Manufacturing

About the role

Argon Medical Devices is seeking a Quality Supervisor to lead the quality function for its medical device manufacturing operations. The role ensures that incoming, in‑process, and finished products meet stringent regulatory and company standards.

Key responsibilities

• Supervise quality personnel and schedule daily inspection, testing, and sampling activities.
• Perform inspections of purchased parts, sub‑assemblies, and finished products using physical, mechanical, and electrical measurement methods.
• Document inspection results, update procedures, protocols, and checklists, and maintain controlled document files.
• Coordinate equipment calibration with the Calibration department and monitor critical instrumentation.
• Review Device History Records (DHRs) and other documentation for compliance with Good Documentation Practices.
• Provide coaching, performance feedback, and disciplinary actions as needed.
• Act as a communication link between management and the quality department.

Required profile

• Experience supervising quality staff in a regulated manufacturing environment.
• Strong understanding of inspection, testing, and calibration processes.
• Ability to interpret and enforce quality procedures and regulatory requirements.
• Excellent organizational and documentation skills.

Required skills

• Inspection and testing of mechanical, electrical, and physical components.
• Calibration coordination and equipment monitoring.
• Device History Record (DHR) review and Good Documentation Practices.