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Medical Device Quality Control Jobs in Wisconsin

Medical Device Quality Inspector Location: Madison, WI Pay Rate: $30/hr. Position Summary: The ... Reports to the Quality Control Manager . * Responsible for timely completion of investigative work ...

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 ...

Senior Quality Manager

Madison, WI · On-site

$130K - $160K/yr

... medical device design and manufacturing site. Utilizes quality statistics to develop effective ... Build, mentor, and lead a high-performing quality assurance and quality control (QA/QC) team ...

Senior Quality Manager

Milwaukee, WI · On-site

$130K - $160K/yr

... medical device design and manufacturing site. Utilizes quality statistics to develop effective ... Build, mentor, and lead a high-performing quality assurance and quality control (QA/QC) team ...

Quality Engineer II

Kenosha, WI

$70K - $90K/yr

... and directs quality control programs designed to ensure continuous production of products ... Knowledge of the medical device manufacturing industry is highly preferred. * Experience with CNC ...

Quality Engineer II

Kenosha, WI · On-site

$70K - $90K/yr

... and directs quality control programs designed to ensure continuous production of products ... Knowledge of the medical device manufacturing industry is highly preferred. * Experience with CNC ...

Medical Device Assembler

Madison, WI · On-site

$23 - $24/hr

Ensure work is completed in compliance with company quality system and medical device regulations. Essential Functions Assemble and test finished and semi-finished medical devices per established ...

Quality Assurance Specialist

Kenosha, WI · On-site

$65K - $75K/yr

Advanced knowledge and experience of the CAPA and complaint process in a medical device manufacturing facility. * Experience with content management/quality systems, archiving and control techniques.

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Medical Device Technician

Madison, WI · On-site

$38K - $48K/yr

Ensure work is completed in compliance with company quality system and medical device regulations. Essential Functions * Assemble, test, and repair work per established work instructions, policies ...

QA Technician

Middleton, WI · On-site

$22 - $25/hr

The Quality Technician you will ensure compliance with medical device quality and regulatory standards by performing incoming inspections, maintaining Device History Records (DHRs), and managing ...

Ensures compliance with the company quality system, in accordance with the applicable Code of ... Ability to create or update service procedures and service manuals as part of the change control ...

Experience or exposure to medical device (Med* Device) quality or regulatory environments. * Strong technical writing skills, with the ability to document investigations, complaints, and reports ...

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Medical Device Quality Control information

See Wisconsin salary details

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$21

$33

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

As of Jul 27, 2026, the average hourly pay for medical device quality control in Wisconsin is $21.68, according to ZipRecruiter salary data. Most workers in this role earn between $17.45 and $24.28 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 quality control in medical devices?

Quality control in medical device manufacturing involves inspecting and testing products to ensure they meet safety, performance, and regulatory standards. Medical device quality control professionals use tools like calibration, documentation, and statistical analysis to identify defects and maintain product consistency throughout production. Compliance with standards such as ISO 13485 is essential in this role.

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 quality control still a job?

Yes, quality control remains a vital role in the medical device industry, ensuring products meet safety and regulatory standards. Quality control professionals typically perform inspections, testing, and documentation, often requiring knowledge of industry regulations and tools like calibration equipment. The role continues to be essential for maintaining product quality and compliance.

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

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.

Do you need a degree for QC?

For a Medical Device Quality Control position, a degree is often preferred but not always required; relevant experience, technical skills, and certifications such as ISO or Six Sigma can also be valuable. Employers may consider candidates with strong attention to detail and knowledge of quality standards even without a formal degree.

What medical device company pays the most?

In the medical device industry, senior quality control roles often have higher salaries, especially at large multinational companies like Medtronic, Abbott, and Johnson & Johnson. Compensation varies based on experience, location, and certifications such as ISO or Six Sigma, but top-paying companies tend to offer competitive salaries for experienced professionals in quality assurance and control positions.
What cities in Wisconsin are hiring for Medical Device Quality Control jobs? Cities in Wisconsin with the most Medical Device Quality Control job openings:
Infographic showing various Medical Device Quality Control job openings in Wisconsin as of July 2026, with employment types broken down into 88% Full Time, 6% Part Time, and 6% Contract. Highlights an 100% In-person job distribution, with an average salary of $45,086 per year, or $21.7 per hour.

Medical Device Quality Inspector

Kellton Tech

Madison, WI • On-site

$30/hr

Contractor

Posted 3 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.