Medical Devices QA Technician

Kerr, part of Envista, is seeking a Quality Assurance professional in Italy to review device history records and drive investigations of nonconformances. You will provide oversight of calibration, validate documentation, and support regulatory reporting.The role requires a bachelor’s degree in a relevant science/engineering field and 5+ years in regulated...

Kerr Italia S.r.l. in Scafati, part of Envista, is seeking a Technician Quality Control to support medical device quality systems.You will review SOPs, test instructions and calibration procedures, and perform final reviews of DHRs, NCRs, and CAPAs while supporting incoming and in-process inspections. The role requires 1–3 years in a regulated environment,...

Envista in Scafati, Campania, seeks a Quality Assurance professional to review manufacturing and quality records, manage nonconformances, CAPAs, and support regulatory reporting in a regulated medical devices environment. ISO 13485 and EU MDR knowledge preferred.You will build quality dashboards, automate workflows with Power BI and Excel, apply AI-enabled...

Envista in Scafati, Campania, seeks a Quality Assurance professional to review manufacturing and quality records, manage nonconformances, CAPAs, and support regulatory reporting in a regulated medical devices environment. ISO 13485 and EU MDR knowledge preferred.You will build quality dashboards, automate workflows with Power BI and Excel, apply AI-enabled...

Envista in Scafati, Campania, seeks a Quality Assurance professional to review manufacturing and quality records, manage nonconformances, CAPAs, and support regulatory reporting in a regulated medical devices environment. ISO 13485 and EU MDR knowledge preferred. You will build quality dashboards, automate workflows with Power BI and Excel, apply...

Envista in Scafati, Campania, seeks a Quality Assurance professional to review manufacturing and quality records, manage nonconformances, CAPAs, and support regulatory reporting in a regulated medical devices environment. ISO 13485 and EU MDR knowledge preferred.You will build quality dashboards, automate workflows with Power BI and Excel, apply AI-enabled...

Key Responsibility • Review documentation for SOP, Test Instruction and Calibration Procedure. • Final review & release of Medical Device History Records (DHRs). • Identify and initiate NCR internal and external (Supplier). • Own and drive CAPA to completion. • Assist with incoming inspection, in process inspection, returns & and continuous...

Job Description: Key Responsibility: • Review documentation for SOP, Test Instruction and Calibration Procedure. • Final review & release of Medical Device History Records (DHRs). • Identify and initiate NCR internal and external (Supplier). • Own and drive CAPA to completion. • Assist with incoming inspection, in process inspection, returns & and...

Job Description * Key Responsibility: Review documentation for SOP, Test Instruction and Calibration Procedure. * Final review & release of Medical Device History Records (DHRs). * Identify and initiate NCR internal and external (Supplier). * Own and drive CAPA to completion. * Assist with incoming inspection, in process inspection, returns & and continuous...