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Quality Control Inspector Medical Devices Jobs (NOW HIRING)

Quality Inspector

Baldwin Park, CA · On-site

$22 - $25/hr

Hands-on experience with quality inspection, quality control, or quality assurance in a manufacturing environment, preferably in medical devices. * Proficiency in blueprint reading and interpreting ...

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Quality Control Inspector -- Urgently hiring in Fountain Valley! Job Title : Quality Control ... medical devices, or advanced electronics; ASQ CQI certification a plus. Why Join Us in Fountain ...

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Position: QC Inspector Reporting Line: QHSE Manager Department: Manufacturing Facility: Lumpkin Rd ... variety of testing devices and procedures to maintain product quality. Essential Duties ...

Position: QC Inspector Reporting Line: QHSE Manager Department: Manufacturing Facility: Lumpkin Rd ... variety of testing devices and procedures to maintain product quality. Essential Duties ...

QC Inspector

O Fallon, MO · On-site

$20 - $23/hr

Anodyne Surgical is looking for a Quality Control Inspector who takes pride in precision and wants ... medical devices. * Comfortable using basic math and computer systems for data entry and review.

QC Inspector

O Fallon, MO · On-site

$20 - $23/hr

Anodyne Surgical is looking for a Quality Control Inspector who takes pride in precision and wants ... medical devices. * Comfortable using basic math and computer systems for data entry and review.

Quality Control Inspector - Welded Products | Manufacturing Environment We are seeking a detail-oriented Quality Control Inspector to support inspection of welded products in a fast-paced ...

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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 May 31, 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 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 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 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.

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.

More about Quality Control Inspector Medical Devices jobs
What cities are hiring for Quality Control Inspector Medical Devices jobs? Cities with the most Quality Control Inspector Medical Devices job openings:
What states have the most Quality Control Inspector Medical Devices jobs? States with the most job openings for Quality Control Inspector Medical Devices jobs include:
Infographic showing various Quality Control Inspector Medical Devices job openings in the United States as of May 2026, with employment types broken down into 2% As Needed, 94% Full Time, 2% Part Time, 1% Temporary, and 1% Nights. Highlights an 98% Physical, and 2% Hybrid job distribution, with an average salary of $44,668 per year, or $21.5 per hour.

Quality Inspector - Medical Devices

SAGE PRODUCT DEVELOPMENT INC

Foxboro, MA

$28 - $35/hr

Full-time

Posted 19 days ago


Job description

Direct Applicants Only. 
COMPANY OVERVIEW:
Sage Product Development, Inc. provides fast, efficient and creative product development and manufacturing services to medical device companies.  We are a focused team of experienced medical device engineers who know what it takes to develop successful products for startups, multinational companies, and everyone in between.
We combine a high level of experience with a low overhead company structure. We are all about solving client companies’ technical challenges and meeting their product development needs in a timely, efficient and highly personalized manner.

GENERAL SUMMARY:
  • Play a key role in ensuring product integrity, compliance, and overall quality throughout the materials control and inspection process.
  • Support incoming inspection of materials, components, and subassemblies used in medical device manufacturing. Ensures suppliers’ products meet specifications and company quality standards to support safe, compliant production.

ESSENTIAL JOB FUNCTIONS:
  • Perform standardized dimensional, mechanical and visual inspection of material, components and subassemblies for size, correct material, finish, appearance, and other pertinent requirements.
  • Verify that materials, equipment, processes, and products comply with quality specifications.
  • Dimensionally inspect products utilizing various measuring devices, such as calipers, micrometers and vision systems.
  • Interpret engineering drawings and specifications and confer with quality, engineering, or leadership staff to determine conformance of product.
  • Participate in maintenance and enhancements to Sage’s materials control system including procurement, incoming inspections, shipping and receiving, kitting, and inventory management.
  • Complete required inspection sheets and forms, maintaining necessary records or audits, dates inspector involved, acceptance or rejection and reasons, etc.
  • Update inventory log and transfer materials, components and subassemblies to warehouse for newly accepted lots.
  • Communicate and collaborate with operations personnel to ensure production needs are met.
  • Work independently and manage daily priorities with minimal supervision.
  • Ensure that work area and equipment are maintained in a clean, safe and orderly condition.
  • Follow all Sage quality systems procedures as applicable.
  • Prepare daily timesheets and submit completed timesheets on a weekly basis.

OTHER DUTIES AND RESPONSIBILITIES
  • Any other duties as assigned.
 
REQUIRED COMPETENCIES
  • Manual dexterity: Skilled hands and excellent hand-eye coordination are required to ensure proper completion of device assembly tasks.
  • Ability to work efficiently and independently is required.
  • The ability to communicate clearly both verbally and in writing is required.
Customer Focus
  • Provide professional, reliable and prompt service to client companies and coworkers. Work in partnership with others to meet or exceed customer expectations. Interpret customers’ needs and take appropriate action. Follow through on customers’ inquiries in a professional and timely manner.
Management of Resources
  • Manage the incoming inspection area. Work in an organized and time effective manner. Take initiative for self-development. Prioritize tasks effectively. Demonstrate initiative and innovation in the use of available resources.
Communication Skills
  • Write and speak in a concise, technically accurate, timely, and professional manner. Exhibit strong verbal presentation and negotiation skills. Interact with client company personnel in a positive and professional manner. Express ideas, recommendations, and solutions clearly, logically, and concisely in both written and verbal communications. Demonstrate tact and diplomacy in communications. Demonstrate active listening skills and ability to resolve discrepancies with customers.

PREPARATION, KNOWLEDGE, SKILLS & ABILITIES:
  • High School diploma, or equivalent.
  • Minimum of 5 years working in a manufacturing/quality environment for medical devices.
  • Proficiency with tools needed for inspection (calipers, micrometers, vision systems, etc.).
  • Proficiency reading and interpreting engineering drawings. Geometric Dimensioning and Tolerancing (GD&T) knowledge.
  • Experience with AQL sampling techniques.
  • Ability to interact with client companies in a professional manner.
  • Flexibility, persistence, resourcefulness, a drive to succeed, and an entrepreneurial spirit.
 
SUPERVISORY RESPONSIBILITY:
  • None.
REPORTS TO:
Director of Manufacturing
Direct Applicants Only. 
WORKING CONDITIONS/PHYSICAL DEMANDS:
  • Must be able to move throughout manufacturing, office and laboratory space, using a complete variety of office equipment, machinery and tools. Must be able to lift more than 25 pounds and stand for extended periods of time.
  • Must be able to wear cleanroom gowning items (head cover, coat, gloves, shoe covers, facial covering if needed) and work in cleanroom environment for extended periods of time.
  • Must be able to work with chemicals found in a manufacturing environment.
  • The above statements are intended to describe the general nature and level of work being performed by people assigned to do this job. The above is not intended to be an exhaustive list of all responsibilities and duties required.
  • External and internal applicants, as well as position incumbents who become disabled as defined under the Americans with Disabilities Act must be able to perform the essential job functions (as listed) either unaided or with the assistance of a reasonable accommodation to be determined by management on a case by case basis.