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Medical Device Manufacturing Engineering Manager Jobs

Medical Device Quality Inspector Location: Madison, WI (Onsite) Pay Rate: $30/hr (W2) Job Summary ... Reports to the Quality Control Manager. * Interfaces primarily with manufacturing, engineering, and ...

The ideal candidate brings strong medical device or equipment manufacturing experience, disciplined ... Engineering team while setting priorities and driving accountability. * Manage a project portfolio ...

Ability to work independently and manage multiple engineering projects Preferred Qualifications * Medical device manufacturing experience * Orthopedic device manufacturing experience * ISO 13485 ...

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Medical Device Manufacturing Engineering Manager information

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$80K

$123.1K

$154K

How much do medical device manufacturing engineering manager jobs pay per year?

As of Sep 13, 2026, the average yearly pay for medical device manufacturing engineering manager in the United States is $123,079.00, according to ZipRecruiter salary data. Most workers in this role earn between $110,000.00 and $136,500.00 per year, depending on experience, location, and employer.

What are popular job titles related to Medical Device Manufacturing Engineering Manager jobs?

For Medical Device Manufacturing Engineering Manager jobs, the most frequently searched job titles are:

Infographic showing various Medical Device Manufacturing Engineering Manager job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 14% Part Time, and 6% Contract. Highlights an 87% Physical, 1% Hybrid, and 12% Remote job distribution, with an average salary of $123,079 per year, or $59.2 per hour.

Medical Device Quality Inspector

Madison, WI • On-site

$30/hr

Contractor

Re-posted 21 days ago


Job description

Job Title: Medical Device Quality Inspector
Location: Madison, WI (Onsite)
Pay Rate: $30/hr (W2)
 

Job Summary

The Medical Device Quality Inspector is responsible for ensuring that materials, processes, and conditions related to the daily manufacturing, processing, and packaging of medical devices meet cGMP standards and comply with internal quality procedures and regulatory standards. This position plays a critical role in ensuring product quality and integrity in a regulated environment.

Essential Functions

  • Perform one of the following Quality department functions:
    • Inspect raw materials to ensure they meet production requirements.
    • Conduct in-process inspections of products and manufacturing processes.
    • Review final documentation and inspect packaging for medical devices, subassemblies, and kits.
  • Assist in documentation control activities within the manufacturing facility.
  • Complete activity documentation and attach appropriate quality status labeling.
  • Ensure proper storage and secure handling of products and labels.
  • Support the Quality team by occasionally conducting nonconformance investigations and assisting with preventive actions.
  • Perform quality reviews for quarantine releases on specific non-reportable, non-complaint materials.

Minimum Requirements

Education & Experience:

  • High School diploma or equivalent required.
  • Minimum 1 year of experience in a regulated work environment preferred.
  • Familiarity with FDA Quality System Regulations and ISO 13485 standards for medical device manufacturing.

Skills & Competencies:

  • Self-motivated and able to work independently.
  • Strong attention to detail.
  • Proficient in using computer-based systems daily.
  • Strong teamwork and collaboration skills.
  • Effective verbal and written communication abilities.

Organizational Relationship / Scope

  • Reports to the Quality Control Manager.
  • Interfaces primarily with manufacturing, engineering, and quality departments to assess nonconforming products and support supplier quality issues.

Working Conditions

  • Work is performed in a controlled environment within a medical device manufacturing facility.
  • Adherence to safety and hygiene protocols is required.