Supervisor Quality Assurance
Core
Supervising Quality Inspection and Non-Conforming Material teams to ensure incoming materials meet high-quality standards for continuous glucose monitoring (CGM) devices.
Role type
Supervisor, Quality Assurance (Medical Devices)
Builds
CGM devices for patients with diabetes
Domain
Medical Devices / Continuous Glucose Monitoring
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Supervision of inspection personnel, 21CFR820 compliance, EN ISO 13485 knowledge, acceptance sampling plans (ANSI/ASQ Z1.4, Z1.9, C=0), Non-conforming Material control, Metrology systems, GDT knowledge, Reading technical drawings and specifications, Inventory management (MRP systems), Continuous improvement project management, Procedure writing, Training personnel, Cross-functional collaboration
Preferred skills
Oracle, 1factory, IQVIA, Reliance, SolidWorks, Vision systems (Keyence, OGP, Mitutoyo), High Gages, CT scanners
Technologies
Oracle, 1factory, IQVIA, Reliance, SolidWorks, Jira, Microsoft Office, MRP systems
Responsibilities
Perform supervisory and administrative duties for Receiving Inspection and QA Support personnel, Coordinate tasks and work plans for Receiving Inspection and Non-Conforming Material areas, Verify accuracy of inspection activities and records in factory inspection systems, Manage material flow, storage, and inventory transactions, Conduct training for personnel, Maintain quality metrics and reports, Identify and implement continuous improvement projects, Write and update area-related procedures, Support inspection of engineering builds, Work across sites to align Receiving Inspection Activities
Seniority
Mid-Senior, Hands-on IC with team lead responsibilities