QC Technician II- Medical Device

Hydrogen Group; Saint Paul (MN); On-site; USD 65,000 - 90,000; Full time

Job summary

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.

Responsibilities

• 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.

Skills

Analytical chemistry understanding

Blueprints & specs reading

Technical writing & reporting

Attention to detail

Auditor liaison

Education

Associate’s degree or higher in STEM

Tools

Gauges

Micrometers

Calipers

Comparators

Microscopes

Job description

As a Senior Quality Assurance Technician, you’ll be the final check on sterile and non-sterile medical devices, carrying out inspections and laboratory testing from incoming materials through to finished product. You’ll run analytical testing using equipment such as UV-Vis, FTIR and particulate analysis, review manufacturing records and supplier data, and make sure only conforming product moves forward. You’ll also own the control of nonconforming and returned material, keeping quarantine areas and records accurate and audit-ready.

Qualifications:

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