ZipRecruiter

Log In

1

Medical Device Quality Investigator Jobs (NOW HIRING)

Kellton Tech

Medical Device Quality Inspector

Madison, WI · On-site

$25 - $30/hr

Medical Device Quality Inspector Location: Madison, WI (Onsite) Pay Rate: $25-30/hr. on W2 **Opportunity to earn overtime pay** The Medical Device Quality Inspection group is responsible for assuring ...

Kellton Tech

Medical Device Quality Engineer

Madison, WI · On-site

$40 - $45/hr

This role oversees CAPA, Change Management, investigations, deviations, Quality Management Reviews ... medical device experience preferred) Skills & Competencies: * Strong communication, coaching ...

Synkriom

Be Seen First

Medical Device Quality Engineer

Warsaw, IN · On-site

$35 - $40/hr

Certified Quality Engineer (CQE) and Medical device, particularly Orthopedic industry, experience preferred Company Description Founded in 2015 and backed by two decades of hands-on experience, our ...

Kyyba Inc

Medical Device Quality Technician

Irving, TX

$21 - $21.98/hr

... medical device assembly. o May operate more advanced measuring instruments as needed. * Perform ... Support Quality Management Systems (QMS), Environmental Management Systems (EMS), and other ...

New

Merck & Co.

$142K - $224K/yr

... root cause investigation of deviations impacting device assembly and packaging ... medical device combination product manufacturing organization.Bachelor's degree in relevant ...

next page

Showing results 1-20

All JobsManufacturing JobsProduct Manufacturing JobsQuality Engineer Medical Device JobsMedical Device Quality Investigator Jobs

Medical Device Quality Investigator information

See salary details

$30.5K

$70.1K

$114K

How much do medical device quality investigator jobs pay per year?

As of Sep 9, 2026, the average yearly pay for medical device quality investigator in the United States is $70,123.00, according to ZipRecruiter salary data. Most workers in this role earn between $50,000.00 and $85,000.00 per year, depending on experience, location, and employer.

What is a medical device quality investigator?

A Medical Device Quality Investigator is a professional responsible for investigating quality issues related to medical devices, such as defects, non-conformities, or customer complaints. Their work involves gathering data, analyzing root causes, and ensuring corrective and preventive actions are implemented to maintain compliance with regulatory standards like FDA and ISO 13485. They collaborate with cross-functional teams to improve product quality and help ensure the safety and effectiveness of medical devices in the market.

What are the key skills and qualifications needed to thrive as a medical device quality investigator?

To thrive as a Medical Device Quality Investigator, you need a strong background in quality assurance, regulatory compliance, and root cause analysis, typically supported by a degree in engineering, life sciences, or a related field. Familiarity with industry standards (such as ISO 13485 or FDA regulations), CAPA management systems, and quality management software is essential. Attention to detail, critical thinking, and effective communication are standout soft skills for this role. These skills ensure thorough investigations, regulatory adherence, and the continuous improvement of device safety and quality.

What are some common challenges faced by medical device quality investigators in conducting root cause analysis?

Medical Device Quality Investigators often face challenges such as limited or incomplete data, complex product designs, and the need to coordinate input from multiple departments during root cause analysis. Investigators must navigate regulatory requirements while ensuring thorough documentation, all within tight deadlines to prevent production delays or recalls. Effective collaboration with engineering, manufacturing, and regulatory teams is essential to accurately identify root causes and implement corrective actions that meet both quality standards and compliance obligations.

What are popular job titles related to Medical Device Quality Investigator jobs?

For Medical Device Quality Investigator jobs, the most frequently searched job titles are:

Infographic showing various Medical Device Quality Investigator job openings in the United States as of September 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $70,123 per year, or $33.7 per hour.

Medical Device Quality Inspector

Madison, WI • On-site

Kellton Tech
See more jobs at Kellton Techexternal

$30/hr

Contractor

Re-posted 17 days ago

Job description

Job Title: Medical Device Quality Inspector
Location: Madison, WI
Pay Rate: $30/hr.

Position Summary:

The Medical Device Quality Inspector is responsible for ensuring that all materials, processes, and packaging activities comply with current GMP standards, FDA regulations, and company quality system requirements. This role plays a critical part in maintaining product integrity, safety, and compliance within a controlled manufacturing environment.

Essential Functions:

  • Perform one or more of the following Quality Department functions:
  • Inspect raw materials to meet production requirements.
  • Conduct in-process inspections of manufacturing products and processes.
  • Review final documentation and shipment packaging for medical devices, subassemblies, and kits.
  • Assist in the Madison Manufacturing documentation control room.
  • Complete documentation of inspection activities, prepare and apply material quality status labels, and ensure proper storage and handling of products and labeling.
  • Support Quality by assisting with nonconformance investigations and preventive actions within the QA unit.
  • Conduct quality reviews for quarantine releases on non-reportable, non-complaint, RMF-3 internal to an RSC.

Minimum Requirements:

Education & Experience:

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

Skills & Competencies:

  • Highly motivated with the ability to work independently.
  • Strong attention to detail and organizational skills.
  • Proficient in the use of computer-based systems.
  • Collaborative mindset; strong engagement both individually and within teams.
  • Excellent verbal and written communication skills.

Organizational Relationships & Scope:

  • Reports to the Quality Control Manager.
  • Responsible for timely completion of investigative work and detailed reporting.
  • Collaborates cross-functionally with Manufacturing, Engineering, and Quality teams to assess nonconforming products and support supplier quality efforts.

Working Conditions:

  • Work performed in a medical device manufacturing facility under controlled environmental conditions.
  • Regular exposure to cleanroom or production environments following standard safety and quality protocols.