Senior QA Technician - Medical Devices Inspection

Hydrogen Group; Saint Paul (MN); Sur place; USD 65 000 - 90 000; Plein temps

Résumé du poste

Hydrogen Group is seeking a Senior Quality Assurance Technician to be the final check on sterile and non-sterile medical devices, performing inspections and lab testing from incoming materials to finished products.

You will run analytical tests (UV-Vis, FTIR, particulates), review manufacturing records and supplier data, and manage nonconforming and returned materials, maintaining quarantine areas and audit-ready documentation.

Qualifications

• Associate’s degree or higher in a STEM subject.
• 3+ years in quality control and inspection within medical device manufacturing.
• Working understanding of analytical chemistry.
• Confidence reading blueprints, specifications and technical procedures.
• Hands-on inspection tools experience: gauges, micrometers, calipers, comparators, microscopes.
• Clear technical writing and reporting skills; able to speak with auditors, suppliers and management.
• Strong attention to detail, including fine visual inspection under magnification.

Responsabilités

• Final check on sterile and non-sterile medical devices.
• Perform inspections and laboratory testing from incoming materials to finished product.
• Run analytical tests using UV-Vis, FTIR and particulate analysis.
• Review manufacturing records and supplier data for conformity.
• Manage nonconforming and returned materials; maintain quarantine areas and audit-ready records.

Connaissances

Analytical chemistry understanding

Blueprints & specs reading

Technical writing & reporting

Attention to detail

Auditor liaison

Formation

Associate’s degree or higher in STEM

Outils

Gauges

Micrometers

Calipers

Comparators

Microscopes

Description du poste

Hydrogen Group is seeking a Senior Quality Assurance Technician to be the final check on sterile and non-sterile medical devices, performing inspections and lab testing from incoming materials to finished products.

You will run analytical tests (UV-Vis, FTIR, particulates), review manufacturing records and supplier data, and manage nonconforming and returned materials, maintaining quarantine areas and audit-ready documentation.