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Quality In Medical Devices Jobs (NOW HIRING)

Manufacturing Engineer- Medical Devices

Maple Grove, MN ยท On-site

$74K - $96K/yr

... quality targets * Design Controls: Participate in design control activities including Design ... Experience with single-use disposable medical devices (catheters, guidewires, or similar products ...

Quality Control Inspector

Irving, TX ยท Hybrid

$23 - $25/hr

... medical devices and entering them into the spinal implant marketplace. We're centrally located in ... Astura's QC Inspector will perform various inspection techniques of medical devices. This position ...

Medical Devices System Engineer

Irvine, CA ยท On-site

$110K - $150K/yr

In this role, you will learn new technologies and lead technical teams to develop systems that ... Recommend and enforce design for compliance to electrical standards for medical devices. * Conduct ...

The ideal candidate is a proactive quality leader with experience in medical devices, healthcare packaging, or other regulated manufacturing environments. They are comfortable balancing strategic ...

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Quality In Medical Devices information

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$38.5K

$91K

$138.5K

How much do quality in medical devices jobs pay per year?

As of Sep 13, 2026, the average yearly pay for quality in medical devices in the United States is $91,047.00, according to ZipRecruiter salary data. Most workers in this role earn between $70,500.00 and $110,000.00 per year, depending on experience, location, and employer.

Quality Engineer - Medical Devices

Minneapolis, MN โ€ข On-site

$75K - $97K/yr

Contractor

Re-posted 25 days ago


Job description

Job Title: Quality Assurance Engineer – Medical Devices

Location: Northwest Minneapolis Metro Area

Type: 6-Month Contract-to-Hire

Job Summary

Seeking a Quality Assurance Engineer to support quality systems, manufacturing operations, CAPA, validation, audits, and DHF activities within a medical device environment. This role will partner cross-functionally to ensure compliance with FDA and ISO standards throughout the product lifecycle.

Key Responsibilities

  • Manage CAPAs, nonconformances, root cause investigations, and change controls
  • Support IQ/OQ/PQ validation activities and review quality documentation
  • Maintain DHF documentation and support product lifecycle activities
  • Review batch records, work orders, and manufacturing documentation for GMP compliance
  • Support incoming inspection, supplier quality, and audit readiness
  • Analyze quality metrics and drive continuous improvement initiatives
  • Support customer complaint investigations and PLM system updates

Required Qualifications

  • Bachelor’s degree in Engineering, Life Sciences, or related field
  • 5+ years of medical device quality or design assurance experience
  • Strong knowledge of FDA 21 CFR 820, ISO 13485, and ISO 14971
  • Experience with CAPA, NCs, DHF, audits, and validation activities
  • Familiarity with PLM systems such as Windchill, Agile, or Propel