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Quality Inspector Medical Device Jobs (NOW HIRING)

Applied Medical

Quality Inspector

Lake Forest, CA · On-site

$18 - $23/hr

Applied Medical is a new generation medical device company with a proven business model and ... The Quality Inspector supports quality control activities, contributes to continuous improvement ...

Applied Medical

Quality Inspector

Lake Forest, CA

$18 - $23/hr

Applied Medical is a new generation medical device company with a proven business model and ... The Quality Inspector supports quality control activities, contributes to continuous improvement ...

Applied Medical

Quality Inspector

Lake Forest, CA · On-site

$18/hr

Applied Medical is a new generation medical device company with a proven business model and ... Position Description The Quality Inspector plays an important role in supporting Applied Medical ...

Lancesoft INC

Assembler (Medical device)

Durham, NC · On-site

$18 - $18.20/hr

Conduct quality inspections on production lines to ensure compliance with standards * Follow SOPs ... Medical device or manufacturing assembly experience * Experience using measuring tools or ...

Ametek

Quality Inspector

Mansfield, MA · On-site

We are searching for a Quality Inspector to be responsible for testing materials and finished ... Experience working in medical device manufacturing * Knowledge and experience with GMP, ISO, FDA ...

Exalta Group

Quality Inspector

Bethlehem, PA · On-site

The Quality Inspector plays a critical role in ensuring Exalta products meet customer specifications, internal quality requirements, and applicable regulatory standards (medical device manufacturing ...

Tegra Medical

Quality Inspector II

Dartmouth, MA · On-site

This also includes any inspections required in support of validation activities. Role and ... Experience in medical device manufacturing preferred. * 3-5 years experience in quality control is ...

Astrix Inc

QC Inspector

Fairfield, CT · On-site

$17 - $22/hr

Pay Rate Low: 17 | Pay Rate High: 22 Our client, a leader in the medical device manufacturing industry, is seeking a QC Inspector to join their team on a contract to hire basis. This role is ...

Synkriom

Be Seen First

Quality Inspector I (Medical Device Manufacturing)

Englewood, CO · On-site

$20 - $24/hr

The Quality Inspector I is responsible for the inspection of materials, assemblies, work-in-progress, and finished medical devices, as well as the completion of documentation to determine conformance ...

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All JobsQuality Inspector Medical Device Jobs

Quality Inspector Medical Device information

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$12

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$32

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

As of Jun 29, 2026, the average hourly pay for quality inspector medical device in the United States is $20.39, according to ZipRecruiter salary data. Most workers in this role earn between $16.11 and $23.08 per hour, depending on experience, location, and employer.

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

AspectQuality Inspector Medical DeviceQuality Technician Medical Device
CertificationsISO 13485, FDA regulations, GMP knowledgeISO 13485, FDA regulations, GMP knowledge
Work EnvironmentManufacturing floors, inspection labsManufacturing floors, inspection labs
Employer & IndustryMedical device manufacturing companiesMedical device manufacturing companies
Primary FocusInspecting and ensuring product qualityPerforming quality checks and supporting inspection processes

The main difference is that Quality Inspector Medical Device roles focus on inspecting and verifying product quality, often involving final inspections and compliance checks. Quality Technicians Medical Device typically support inspection processes, perform routine tests, and assist inspectors. Both roles require similar certifications and work environments, but inspectors have a more oversight-oriented responsibility, while technicians support the inspection process.

What are some common challenges Quality Inspectors face in the medical device industry, and how can they effectively address them?

Quality Inspectors in the medical device sector often encounter challenges such as keeping up with strict regulatory standards, ensuring accurate documentation, and identifying subtle product defects. To address these, inspectors need to stay updated on the latest industry regulations (such as FDA and ISO standards), use precise measuring tools, and maintain clear communication with manufacturing and engineering teams. Regular training and collaboration with cross-functional teams can help inspectors remain vigilant and contribute to a culture of quality and compliance.

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

A Quality Inspector in the medical device industry is responsible for examining products and components to ensure they meet strict regulatory and company standards. They perform inspections during various stages of the manufacturing process, use specialized tools to measure and test products, and document any defects or non-conformance. Their role is crucial in ensuring patient safety and compliance with regulations set by agencies such as the FDA and ISO. Quality Inspectors also help identify areas for process improvement to maintain high-quality standards.

What are the key skills and qualifications needed to thrive as a Quality Inspector in the medical device industry, and why are they important?

To thrive as a Quality Inspector in the medical device industry, you need a solid understanding of quality assurance principles, regulatory standards (such as ISO 13485 or FDA requirements), and experience with inspection procedures, often supported by a relevant technical diploma or degree. Familiarity with inspection tools like calipers, micrometers, and visual inspection systems, as well as quality management software, is typically required. Attention to detail, analytical thinking, and effective communication are crucial soft skills for ensuring product compliance and reporting issues. These skills and qualifications are vital to maintain consistent product safety and quality, ensuring compliance with strict regulatory standards and protecting patient health.
More about Quality Inspector Medical Device jobs
What states have the most Quality Inspector Medical Device jobs? States with the most job openings for Quality Inspector Medical Device jobs include:
What job categories do people searching Quality Inspector Medical Device jobs look for? The top searched job categories for Quality Inspector Medical Device jobs are:
Quality Inspector Medical Device jobs near you
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.