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Medical Device Quality Control Jobs in Minnesota

CAERUS CORP

Quality Control Inspector

Blaine, MN

$20 - $25/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Quality Control Inspector Schedule: B: Monday - Thursday, 5pm - 3:30am Pay Range: $20.00 - $25.00 ... Why Join Us? * We're a mid-sized medical device contract manufacturer, which means you get the best ...

Caerus Corp

Quality Control Inspector

Blaine, MN · On-site

$20 - $25/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Quality Control Inspector Schedule: B: Monday - Thursday, 5pm - 3:30am Pay Range: $20.00 - $25.00 ... Why Join Us? * We're a mid-sized medical device contract manufacturer, which means you get the best ...

Merit

Quality Control Technician

Hills, MN

$23 - $31/hr

  • Medical

  • Retirement

  • PTO

Experience working in a medical device environment. COMPETENCIES Organization Interpersonal Skills ... Control Risk Category II: The risk category explains whether or not employees are likely to come ...

Coloplast

Quality Engineer

Plymouth, MN · On-site

$88K - $98K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Working knowledge of medical device regulations (Regulation 2017/745 (EU MDR), US 21 CFR Part 820). * ASQ Certified Quality Engineer preferred. Required Knowledge, Skills and Abilities * Working ...

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Medical Device Quality Control information

See Minnesota salary details

$11

$21

$32

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

As of Aug 20, 2026, the average hourly pay for medical device quality control in Minnesota is $21.03, according to ZipRecruiter salary data. Most workers in this role earn between $16.97 and $23.56 per hour, depending on experience, location, and employer.

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.

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.

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 are popular job titles related to Medical Device Quality Control jobs in Minnesota?

For Medical Device Quality Control jobs in Minnesota, the most frequently searched job titles are:

What job categories do people searching Medical Device Quality Control jobs in Minnesota look for?

The top searched job categories for Medical Device Quality Control jobs in Minnesota are:

What cities in Minnesota are hiring for Medical Device Quality Control jobs?

Cities in Minnesota with the most Medical Device Quality Control job openings:

Medical Device Quality Control jobs near you
Infographic showing various Medical Device Quality Control job openings in Minnesota as of August 2026, with employment types broken down into 1% As Needed, 76% Full Time, 15% Part Time, 7% Contract, and 1% Nights. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $43,749 per year, or $21 per hour.

Medical Device Complaint Specialist

Three Point Solutions, Inc.

Moundsview, MN • On-site

Full-time

Re-posted yesterday

Job description

Job title : Medical Device Complaint Specialist
Client : Medical Device Manufacturing Company
Duration : 24 Months
Location : Mounds View, MN 55112
Shift : 1st Shift (Hybrid - 4 Days Onsite, 1 Day Remote)
Description:
  • Support Medical Device Report (MDR) activities.
  • Review and process complaint records.
  • Manage adverse event reporting.
  • Monitor medical device surveillance.
  • Maintain MDR and ADE records.
  • Review clinical safety data.
  • Prepare safety summaries and reports.
  • Ensure regulatory compliance.
  • Support complaint investigations.
  • Collaborate with cross-functional teams.
  • Maintain quality documentation.
  • Support regulatory reporting projects.

Required Qualifications:
  • Bachelor's degree required.
  • 1-3 years of relevant experience.
  • Medical Device Reporting (MDR) experience.
  • Complaint handling experience.
  • Knowledge of regulatory compliance.
  • Strong analytical and critical thinking skills.
  • Excellent organizational and time management skills.
  • Strong written communication.
  • Attention to detail.
  • Ability to manage multiple priorities.

Preferred Qualifications:
  • Clinical background (RN or Healthcare Professional).
  • Biomedical Engineering background.
  • Experience in a regulated environment.
  • Knowledge of quality systems.
  • Medical device industry experience.
  • Experience with adverse event reporting.
  • Cross-functional collaboration experience.

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