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Entry Level Medical Device Quality Assurance Jobs

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 ...

Saxon Global

QA ENGINEER

Saint Augustine, FL · On-site

Medical Device Quality Engineer Position Type :Contract Projected Start Date :08-09-2017 Zip Code :33716 City :St. Petersburg State :FL Required Skills : ISO 9000 Not looking for a Design or testing ...

KYYBA

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Medical Device Quality Control Technician

Atlanta, GA · On-site

$25 - $27.50/hr

At least one year in quality assurance role in medical device industry is preferred. Language Skills · Ability to read and interpret documents such as safety rules, operating and maintenance ...

Marquee Staffing - OC

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Medical Device Assembler, Weekend Day 3/12 Schedule

Irvine, CA · On-site

$19 - $20/hr

Medical Device implant manufacturer in Irvine is seeking applicants with manufacturing experience ... quality assurance program, as well as safety and environmental standards. Ability to establish ...

Applied Medical

Quality Inspector

Lake Forest, CA · On-site

$18/hr

... for medical device manufacturing and quality assurance. Key Responsibilities * Perform First ... Experience working with the SAP enterprise system. * Entry-level understanding of inspecting raw ...

Applied Medical

Quality Inspector

Lake Forest, CA

$18 - $23/hr

... for medical device manufacturing and quality assurance. Key Responsibilities * Perform First ... Experience working with the SAP enterprise system. * Entry-level understanding of inspecting raw ...

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Entry Level Medical Device Quality Assurance information

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How much do entry level medical device quality assurance jobs pay per hour?

As of Aug 18, 2026, the average hourly pay for entry level medical device quality assurance in the United States is $29.29, according to ZipRecruiter salary data. Most workers in this role earn between $18.75 and $34.38 per hour, depending on experience, location, and employer.

What is an entry level medical device quality assurance?

An Entry Level Medical Device Quality Assurance (QA) job involves ensuring that medical devices meet regulatory standards and company quality requirements. Individuals in this role assist with tasks such as inspecting products, documenting processes, performing tests, and supporting audits. They work closely with engineering, manufacturing, and regulatory teams to help maintain product safety and quality. Entry-level QA professionals typically learn about relevant regulations, such as FDA and ISO standards, and help implement quality control procedures. This role is a great starting point for a career in medical device quality management.

What are the key skills and qualifications needed to thrive as an entry level medical device quality assurance professional?

To thrive as an Entry Level Medical Device Quality Assurance professional, you typically need a bachelor's degree in a science or engineering field, strong analytical skills, and a solid understanding of quality principles and regulatory standards. Familiarity with quality management systems (such as ISO 13485), document control software, and basic statistical analysis tools is highly valuable. Attention to detail, effective communication, and a willingness to learn are important soft skills for this role. These skills and qualities are essential to ensure product safety, regulatory compliance, and continuous quality improvement in the medical device industry.

What are some typical challenges faced by entry level medical device quality assurance professionals?

Entry-level professionals in medical device quality assurance often encounter challenges such as learning to navigate complex regulatory requirements (like FDA or ISO standards), understanding technical documentation, and maintaining meticulous attention to detail during inspections and audits. Adaptability is key, as priorities can shift quickly in response to production needs or regulatory updates. Additionally, collaborating effectively with cross-functional teams—such as engineering, manufacturing, and regulatory affairs—is essential for ensuring product quality and compliance.

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

AspectEntry Level Medical Device Quality AssuranceQuality Control Technician
CertificationsISO 13485, FDA regulations, GMP knowledgeGMP, ISO 9001, basic technical certifications
Work EnvironmentManufacturing, R&D, regulatory compliance settingsProduction lines, inspection labs
Employer & Industry UsageMedical device companies, biotech firmsManufacturers, quality departments
Search & Comparison IntentUnderstanding QA roles in medical devicesTechnical inspection and testing roles

Entry Level Medical Device Quality Assurance focuses on ensuring compliance with regulations, documentation, and process audits, while Quality Control Technicians primarily perform product inspections and testing. Both roles are essential in manufacturing but differ in scope and responsibilities.

More about Entry Level Medical Device Quality Assurance jobs

What cities are hiring for Entry Level Medical Device Quality Assurance jobs?

Cities with the most Entry Level Medical Device Quality Assurance job openings:

What are the most commonly searched types of Medical Device Quality Assurance jobs?

The most popular types of Medical Device Quality Assurance jobs are:

What states have the most Entry Level Medical Device Quality Assurance jobs?

States with the most job openings for Entry Level Medical Device Quality Assurance jobs include:

What job categories do people searching Entry Level Medical Device Quality Assurance jobs look for?

The top searched job categories for Entry Level Medical Device Quality Assurance jobs are:

Entry Level Medical Device Quality Assurance jobs near you
Infographic showing various Entry Level Medical Device Quality Assurance job openings in the United States as of August 2026, with employment types broken down into 33% Full Time, and 67% Contract. Highlights an 100% In-person job distribution, with an average salary of $60,925 per year, or $29.3 per hour.

Medical Device Quality Inspector

Kellton Tech

Madison, WI • On-site

$30/hr

Contractor

Re-posted 25 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.