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Medical Device Quality Control Jobs (NOW HIRING)

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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 ...

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Medical Device Quality Inspector Location: Madison, WI (Onsite) Pay Rate: $30/hr (W2) Job Summary ... Reports to the Quality Control Manager. * Interfaces primarily with manufacturing, engineering, and ...

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 ...

Job Title: Medical Device Quality Engineer Location: Madison, WI Pay Rate : $40--45/hr on W2 ... Quality Control, Engineering, Facilities, Materials Management, Regulatory Affairs, and Process ...

QC Technician - Medical Device

Irvine, CA · On-site

$20.63 - $25.65/hr

... device combination products for the treatment of coronary and peripheral artery disease. Our ... medical needs. Responsibilities The Quality Control Technician I is responsible for reviewing ...

... device combination products for the treatment of coronary and peripheral artery disease. Our ... medical needs. Responsibilities The Quality Control Technician I is responsible for reviewing ...

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Medical Device Quality Control information

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$11

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$33

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

As of Aug 17, 2026, the average hourly pay for medical device quality control 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 in a medical device quality control role, and how can I prepare for them?

Professionals in Medical Device Quality Control often face challenges such as keeping up with evolving regulatory standards, managing documentation for audits, and ensuring consistent product quality across batches. To prepare, it's helpful to develop strong attention to detail, stay updated on FDA and ISO guidelines, and build effective communication skills to collaborate with cross-functional teams like manufacturing and R&D. Being proactive in identifying potential risks and participating in continuous improvement initiatives can also help you succeed in this role.

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

AspectMedical Device Quality ControlMedical Device Quality Assurance
FocusInspecting and testing products to identify defectsDeveloping and maintaining quality systems and processes
ActivitiesProduct testing, inspection, samplingAudits, process validation, compliance management
CertificationsISO 13485, GMP trainingISO 13485, regulatory standards
Work EnvironmentLaboratories, manufacturing floorsQuality departments, regulatory offices

Medical Device Quality Control focuses on testing and inspecting products to ensure they meet quality standards, while Medical Device Quality Assurance emphasizes establishing systems and processes to prevent defects and ensure compliance. Both roles are essential in maintaining high-quality medical devices and often work closely within the industry.

What is medical device quality control?

Medical Device Quality Control refers to the processes and procedures used to ensure that medical devices meet safety, quality, and regulatory standards before they reach the market. This involves rigorous inspection, testing, and documentation throughout the manufacturing process to prevent defects and ensure consistent product performance. Quality control professionals work to identify issues, monitor compliance with industry regulations like ISO 13485 and FDA requirements, and help maintain the integrity of healthcare products. Their role is crucial in protecting patient safety and upholding the reputation of medical device manufacturers.

Is medical device quality control a good career?

Medical device quality control involves inspecting and testing devices to ensure they meet safety and regulatory standards, often requiring knowledge of quality management systems and industry regulations. It offers stable employment opportunities with potential for advancement and typically requires attention to detail and relevant certifications. The field is essential for patient safety and is considered a reliable career path within the healthcare manufacturing industry.

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

To thrive in Medical Device Quality Control, you need a solid understanding of quality assurance principles, regulatory standards (such as ISO 13485 or FDA 21 CFR Part 820), and experience with inspection techniques, often supported by a degree in engineering or life sciences. Familiarity with tools like statistical process control (SPC) software, electronic quality management systems (eQMS), and documentation protocols is typical. Attention to detail, problem-solving abilities, and strong communication skills are essential soft skills for excelling in this role. These competencies are crucial for ensuring product safety, regulatory compliance, and maintaining the reputation of the medical device manufacturer.
More about Medical Device Quality Control jobs

What cities are hiring for Medical Device Quality Control jobs?

Cities with the most Medical Device Quality Control job openings:

What states have the most Medical Device Quality Control jobs?

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

Infographic showing various Medical Device Quality Control job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% 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.

Medical Device Quality Control Technician

KYYBA

Atlanta, GA • On-site

$25 - $27.50/hr

Contractor

PTO

Posted 2 days ago

New

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Job description

Qualifications

·        To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

·        Ability to follow Good Manufacturing/Laboratory Practices (GMP and GLP)

Education and/or Experience

·        Bachelor's degree in a scientific or technical area or equivalent combination of experience and education. 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 instructions, and procedure manuals. Ability to write routine reports and correspondence. Ability to speak effectively before small groups of customers or employees of organization.

Computer Skills

·        To perform this job successfully, an individual should have knowledge of Database software; Internet software; Inventory software; Spreadsheet software and Word Processing software.

Other Skills and Abilities

·        Ability to follow procedures and accurately document results

·        Understanding the manufacturing processes of Company products and ability to recognize deviations from approved documented procedures

·        Attention to detail.

Ability to use bleach for cleaning purposes is required..

Company Description

Founded in 1998 and headquartered in Farmington Hills, MI, Kyyba has a global presence delivering high-quality resources and top-notch recruiting services, enabling businesses to effectively respond to organizational changes and technological advances.

At Kyyba, the overall well-being of our employees and their families is important to us. We are proud of our work culture which embodies our core values; incorporating value, passion, excellence, empowerment, and happiness, creates a vibrant and productive atmosphere. We empower our employees with the resources, incentives, and flexibility that they need to support a healthy, balanced, and fulfilling career by providing many valuable benefits and a balanced compensation structure combined with career development.

Kyyba is an Equal Opportunity Employer.

Kyyba does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, non-disqualifying physical or mental disability, national origin, veteran status or any other b


KYYBA logo

About KYYBA

Sourced by ZipRecruiter

About Kyyba: Founded in 1998 and headquartered in Farmington Hills, MI, Kyyba has a global presence delivering high-quality resources and top-notch recruiting services, enabling businesses to effectively respond to organizational changes and technological advances. At Kyyba, the overall well-being of our employees and their families is important to us. We are proud of our work culture which embodies our core values; incorporating value, passion, excellence, empowerment, and happiness, creates a vibrant and productive atmosphere. We empower our employees with the resources, incentives, and flexibility that they need to support a healthy, balanced, and fulfilling career by providing many valuable benefits and a balanced compensation structure combined with career development.

Industry

Recruiting and staffing services

Company size

501 - 1,000 Employees

Headquarters location

Farmington Hills, MI, US

Year founded

1998

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