ZipRecruiter

Log In

1

Medical Device Quality Control Inspector Jobs (NOW HIRING)

Regal Staffing Services

QC Inspector Lead

Midlothian, TX · On-site

$20 - $25/hr

Minimum 2 years of hands-on experience as Quality Control Lead Inspector in cGMP environment; preferably in pharmaceutical, biomedical, or medical device field (regulated industry) * Ability to ...

Medical Device Manufacturing Co

Be Seen First

Quality Control Inspector

Pompano Beach, FL · On-site

$17/hr

... device inspection by measuring dimensions, such as length, diameter, and distance between reference points, using precision instruments such as micrometers, calipers, comparators to ensure product(s ...

Arthrex

Quality Control Inspector II

Santa Barbara, CA · On-site

$1.5K/wk

Join our talented team at a growing global medical device company focused on Helping Surgeons Treat Their Patients Better™. Essential Duties and Responsibilities * Performs and documents ...

Summa

QC Inspector

Houston, TX · On-site

$20 - $25/hr

Compensation: 20-25/hr Summary We're working with a growing medical device manufacturer looking to add a QA Inspector focused on incoming quality control. This role supports inspection of raw ...

ARTHREX

Quality Control Inspector II

Santa Barbara, CA · On-site

$1.5K/wk

Salary Minimum: $21.85 Salary Maximum: $29.65 Arthrex, Inc. is a global medical device company and ... The QC Inspector performs a variety of quality control test and inspection functions on materials ...

previous pagenext page

Showing results 21-40

All JobsManufacturing JobsProduct Manufacturing JobsQuality Control Inspector JobsMedical Device Quality Control Inspector Jobs

Medical Device Quality Control Inspector information

See salary details

$11

$21

$33

How much do medical device quality control inspector jobs pay per hour?

As of Sep 10, 2026, the average hourly pay for medical device quality control inspector in the United States is $21.48, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $24.04 per hour, depending on experience, location, and employer.

What does a medical device quality control inspector do?

A Medical Device Quality Control Inspector is responsible for examining medical devices during and after production to ensure they meet all regulatory, quality, and safety standards. This involves inspecting products for defects, verifying measurements, and ensuring compliance with industry regulations such as FDA and ISO standards. Inspectors document their findings, report any issues, and may recommend corrective actions to improve quality. Their work is critical to ensuring that only safe and effective medical devices reach healthcare providers and patients.

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

To excel as a Medical Device Quality Control Inspector, you need a solid understanding of quality assurance principles, regulatory standards (such as ISO 13485 or FDA requirements), and a background in science or engineering. Familiarity with inspection tools like calipers, micrometers, and statistical process control software is typically required, along with any relevant quality certifications (e.g., ASQ CQI). Attention to detail, analytical thinking, and effective communication are crucial soft skills for identifying defects and collaborating with production teams. These competencies ensure product safety, regulatory compliance, and the consistent delivery of high-quality medical devices.

What are some common challenges faced by medical device quality control inspectors, and how can they be addressed?

Medical Device Quality Control Inspectors often face challenges such as keeping up with evolving regulatory standards, ensuring precise documentation, and maintaining consistency during inspections of complex products. To address these, inspectors should stay updated through regular training, closely follow Standard Operating Procedures (SOPs), and use checklists to ensure thoroughness. Collaboration with engineering, production, and regulatory teams is also essential to resolve issues promptly and ensure compliance with industry regulations.

What is the difference between Medical Device Quality Control Inspector vs Quality Assurance Technician?

AspectMedical Device Quality Control InspectorQuality Assurance Technician
CertificationsISO 13485, FDA regulationsISO 9001, GMP training
Work EnvironmentManufacturing, lab settingsProduction lines, labs
Employer & IndustryMedical device manufacturingVarious manufacturing sectors

The Medical Device Quality Control Inspector focuses on inspecting and testing medical devices to ensure compliance with industry standards, while the Quality Assurance Technician oversees broader quality processes, including documentation and process improvements. Both roles require similar certifications and often work in manufacturing environments, but their primary responsibilities differ in scope and focus.

What states have the most Medical Device Quality Control Inspector jobs?

States with the most job openings for Medical Device Quality Control Inspector jobs include:

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

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

Infographic showing various Medical Device Quality Control Inspector 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 $44,668 per year, or $21.5 per hour.

Quality Control Manager / Supervisor (Medical Device Manufacturing)

Gardner, MA • On-site

Corporate Solutions Tech
Recruiting and Staffing Services • 11 - 50 employees
Learn more about Corporate Solutions Techexternal

Full-time

Posted 19 days ago

Job description

Job Summary

We are seeking a Quality Control Manager / Supervisor to lead Quality Control activities within a regulated medical device contract manufacturing environment. This position will oversee a team of approximately 4–5 direct reports and be responsible for quality control operations, inspection, calibration, product release, DHR review, nonconforming material controls, and continuous improvement.

The ideal candidate will have strong experience in medical device manufacturing, metrology, calibration systems, and quality control, along with proven supervisory or management experience.

Responsibilities
  • Manage daily Quality Control operations, including inspection, testing, review, and release of materials and finished medical devices.
  • Establish priorities and allocate resources while maintaining production schedules and quality requirements.
  • Develop, implement, and maintain QC procedures, work instructions, inspection methods, and acceptance criteria.
  • Oversee incoming inspection of components, raw materials, labels, packaging materials, and outsourced manufacturing services.
  • Support supplier quality activities and supplier corrective actions.
  • Manage final inspection, product testing, and product acceptance activities.
  • Review quality records supporting final product acceptance.
  • Authorize or oversee final release of finished medical devices.
  • Perform or oversee comprehensive Device History Record (DHR) reviews.
  • Ensure manufacturing and inspection records are complete, accurate, and traceable.
  • Administer and continuously improve the calibration program for inspection, measuring, and test equipment.
  • Coordinate external calibration vendors and service providers.
  • Manage qualification, maintenance, and monitoring of QC equipment.
  • Identify, document, segregate, and control nonconforming materials and products.
  • Participate in MRB activities and support investigations involving nonconformances, complaints, CAPAs, and audits.
  • Lead, coach, mentor, and develop Quality Control Inspectors and Technicians.
  • Conduct training, qualification, and competency assessments.
  • Establish departmental goals and performance metrics.
  • Support internal, customer, supplier, and regulatory audits.
  • Participate in CAPA investigations and process improvement initiatives.
  • Support risk management activities and Quality Management System improvements.
  • Analyze quality metrics and identify opportunities for continuous improvement.
  • Promote a culture of quality, compliance, accountability, and continuous improvement.
Required Qualifications
  • 5+ years of Quality Control, Quality Assurance, or Manufacturing Quality experience within the medical device industry.
  • Minimum 2–3 years of leadership or supervisory experience.
  • Medical device manufacturing experience required.
  • Experience with:
    • Incoming inspection
    • Final product inspection
    • Product release
    • DHR review
    • Calibration management
    • Nonconforming material disposition
    • CAPA participation
    • Internal and external audits
  • Strong knowledge of FDA 21 CFR Part 820 and ISO 13485.
  • Knowledge of metrology and calibration systems.
  • Familiarity with Gage R&R and measurement system analysis.
  • Ability to interpret engineering drawings, specifications, and test methods.
  • Knowledge of statistical sampling plans and inspection techniques.
  • Strong technical writing and documentation skills.
  • Excellent organizational, problem-solving, verbal, and written communication skills.
  • Ability to lead cross-functional teams and influence decision-making.
  • ERP, Electronic QMS, and calibration management system experience preferred.
Education
  • Bachelor's degree in Engineering, Quality, Life Sciences, Manufacturing, or a related technical discipline required.
  • Equivalent combination of education and relevant experience may be considered.
Preferred Qualifications
  • ASQ CQE, CQA, or CQT certification.
  • ISO 13485 Lead Auditor certification.
  • Experience with electronic and paper-based DHR systems.
  • Experience with validation activities, including IQ/OQ/PQ.
  • Contract manufacturing experience preferred.
  • Class II medical device experience or higher preferred.
  • Experience managing calibration and preventative maintenance systems.
  • Experience with supplier management, SCARs, return-to-vendor processes, and final batch release.
  • Ability to read engineering drawings and understand dimensions.