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Quality Control Inspector Medical Devices Jobs (NOW HIRING)

DPR Construction

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Quality Control Inspector

Phoenix, AZ · On-site

$18 - $35/hr

Able to operate electronic devices such as iPhone, iPad, and capable to use Microsoft suite ... Including medical, dental, and vision. · Financial Security: With a 401K plan and AD&D insurance ...

Endologix

Quality Control Inspector

Santa Rosa, CA

Overview Join our mission-driven Quality team as the Quality Control Inspector at Endologix! WHO WE ... and finished medical devices to ensure compliance with quality standards and regulatory ...

Endologix

Quality Control Inspector

Santa Rosa, CA · On-site

Overview Join our mission-driven Quality team as the Quality Control Inspector at Endologix! WHO WE ... and finished medical devices to ensure compliance with quality standards and regulatory ...

Aerotek

QC Inspector

Garland, TX

Job Title: QC Inspector The QC Inspector performs detailed in-process and final inspections of ... medical devices, serving as a critical gatekeeper for quality. The organization offers strong ...

KRYPTON SOLUTIONS LLC

QC Inspector

Plano, TX · On-site

You will have benefits such as Medical, Dental, Vision, 401(k), Life Insurance, and Paid Time Off ... Make a difference as a QC Inspector As a QC Inspector at Krypton Solutions, your daily ...

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Quality Control Inspector Medical Devices information

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$33

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

As of Jun 29, 2026, the average hourly pay for quality control inspector medical devices 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 are some common challenges faced by Quality Control Inspectors in the medical device industry, and how can they be addressed?

Quality Control Inspectors in the medical device industry often face challenges such as keeping up with rigorous and evolving regulatory standards, ensuring consistent documentation, and identifying subtle defects in highly technical products. To address these, inspectors should stay updated on industry regulations (like FDA and ISO standards), follow standardized inspection protocols, and participate in ongoing training. Collaboration with engineering and manufacturing teams is also essential to resolve non-conformances quickly and maintain high product quality.

What are the key skills and qualifications needed to thrive as a Quality Control Inspector in Medical Devices, and why are they important?

To thrive as a Quality Control Inspector in Medical Devices, you need a solid understanding of quality assurance principles, knowledge of regulatory standards like ISO 13485, and a background in life sciences or engineering. Familiarity with inspection tools (calipers, micrometers), statistical process control software, and documentation systems is typically required. Attention to detail, strong analytical thinking, and effective communication distinguish top performers in this position. These skills ensure product safety and compliance, which are critical for patient health and regulatory approval.

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

AspectQuality Control Inspector Medical DevicesQuality Assurance Technician Medical Devices
CertificationsOften requires GMP, ISO 13485, or specific industry certificationsSimilar certifications, with additional focus on QA methodologies
Work EnvironmentLaboratory, manufacturing floor, inspection stationsQuality labs, production areas, documentation review
Primary FocusInspecting products for defects, ensuring compliance with specificationsDeveloping and maintaining quality systems, process improvements
Employer & Industry UsageMedical device manufacturing companies, suppliersMedical device companies, regulatory agencies

While both roles focus on quality in medical device manufacturing, the Quality Control Inspector Medical Devices primarily conducts product inspections to identify defects, whereas the Quality Assurance Technician Medical Devices develops and maintains quality systems to prevent defects. Both roles require similar certifications and work environments, but their core responsibilities differ in scope and focus.

What does a Quality Control Inspector do in the medical device industry?

A Quality Control Inspector in the medical device industry is responsible for ensuring that products meet established safety and quality standards. They examine materials, components, and finished devices for defects or deviations from specifications. Inspectors use specialized tools and testing procedures to verify product compliance with regulatory requirements, such as those set by the FDA or ISO. Their work is critical to maintaining patient safety and ensuring that only high-quality devices reach the market.
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Quality Control Inspector Medical Devices jobs near you
Infographic showing various Quality Control Inspector Medical Devices job openings in the United States as of June 2026, with employment types broken down into 2% As Needed, 24% Full Time, 45% Part Time, and 29% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $44,668 per year, or $21.5 per hour.
Quality Control Inspector (Medical Device / GMP)

Quality Control Inspector (Medical Device / GMP)

Intellectt INC

Portland, OR • On-site

Contractor

Posted 28 days ago

Job description

Role: Quality Control Inspector
Location: Portland, OR - 97224
Duration: 7 Months
Shift Timings: 8 AM to 4:30 PM
 
 
Job Description:
The Inspector performs basic routine inspection of electronic, electro-mechanical and/or mechanical materials, components and sub-assemblies received, in process of manufacture, or manufactured, for conformance with quality assurance standards.
Key Job Duties and Responsibilities:
Inspection & Testing: Performs visual and physical inspections of raw materials, in-process components, and finished products to ensure they meet quality specifications.
Uses precision measuring tools and lab equipment to verify product dimensions and performance.
Documentation & Compliance: Accurately maintains Lot History Records (LHR), batch records, and inspection logs in compliance with Good Documentation Practices (GDP) and FDA regulations.
Defect Management: Identifies, classifies, and reports defects.
Manages non-conforming material by initiating Non-Conformance Reports (NCR) and assisting with investigations.
Process Control: Monitors production processes to ensure adherence to standard operating procedures (SOPs) and Good Manufacturing Practices (GMPs).
Equipment Maintenance: Calibrates, cleans, and performs routine maintenance on inspection and testing equipment to ensure accuracy.
Collaboration: Works with production and engineering teams to support quality improvements, provide feedback on product quality, and ensure regulatory compliance.
 
Key Competencies:
Attention to Detail: High level of accuracy in documentation and inspection.
Computer Literacy: Proficient in using software like SAP, POMS, or Laboratory Information Management Systems (LIMS).
Technical Knowledge: Understanding of ISO 13485 and FDA 21 CFR Part 820 regulations.
Communication: Ability to clearly report deviations and collaborate in a team environment.
Common Educational/Experience Requirements:
High school diploma or equivalent is required. Associate’s or Bachelor’s degree in a technical field preferred.
Previous experience in manufacturing, particularly in medical device, pharmaceutical, or similar regulated industries is highly desired.
1+ years of experience desired.