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Medical Device Quality Control Jobs in Arizona (NOW HIRING)

Hanger, Inc.

QA/QC Engineer I

Phoenix, AZ

$27.02 - $40.48/hr

... medical device regulations, including 21 CFR 820, the Medical Device Directive (MDD), ISO 13485 ... Support QA/QC activities by following established procedures and requirements related to 21 CFR 820 ...

onsemi

Sr. Customer Quality Manager

Scottsdale, AZ · On-site

$140 - $180/hr

... control in the semiconductor industry. Medical device exp. is a plus. * Background in customer-facing roles, semiconductor, and/or the Medical Industry, and strategic leadership * Hands-on skills in ...

Hanger

QA/QC Engineer I

Phoenix, AZ · On-site

$60 - $80/hr

Support QA/QC activities by following established procedures and requirements related to 21 CFR 820 ... Some experience in the medical device industry, quality assurance, regulatory affairs, or a related ...

GN Group

Medical Device Sales

Prescott, AZ · On-site

$76.50 - $93.50/hr

Medical Device Sales - Prescott, Arizona****Salary Potential:**$2,500/month while training. When ... Beltone remains the most trusted brand for quality products and care among its patients and adults ...

Hanger, Inc.

QA/QC Engineer I

Phoenix, AZ · On-site

Support QA/QC activities by following established procedures and requirements related to 21 CFR 820 ... Some experience in the medical device industry, quality assurance, regulatory affairs, or a related ...

Hanger, Inc.

QA/QC Engineer I

Phoenix, AZ

Support QA/QC activities by following established procedures and requirements related to 21 CFR 820 ... Some experience in the medical device industry, quality assurance, regulatory affairs, or a related ...

Gn

Medical Device Sales

Prescott, AZ · On-site

$85K/yr

Medical Device Sales - Prescott, Arizona Salary Potential: $2,500/month while training. When ... Beltone remains the most trusted brand for quality products and care among its patients and adults ...

Beltone

Medical Device Sales

Prescott, AZ

$85K/yr

Medical Device Sales - Prescott, Arizona Salary Potential: $2,500/month while training. When ... Beltone remains the most trusted brand for quality products and care among its patients and adults ...

Beltone

Medical Device Sales

Prescott, AZ · On-site

$85K/yr

Medical Device Sales - Prescott, Arizona Salary Potential: $2,500/month while training. When ... Beltone remains the most trusted brand for quality products and care among its patients and adults ...

Herbally Yours Inc

Production QC Technician

Gilbert, AZ · On-site

$25 - $30/hr

We are looking for an experienced Production QC Technician to join our manufacturing team. This is ... Dietary supplement, nutraceutical, food/beverage, cosmetics, pharmaceutical, medical device, or ...

System One

Quality Control Associate

Oro Valley, AZ · On-site

$25.75/hr

Responsible for generating compliant QC documentation as part of the Device History Record required ... medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as ...

CYNET SYSTEMS

Quality Control Associate

Tucson, AZ · On-site

$25/hr

Responsible for generating compliant QC documentation as part of the Device History Record required for releasing items into inventory from the raw material to the in-process finished goods.

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Medical Device Quality Control information

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

As of Sep 5, 2026, the average hourly pay for medical device quality control in Arizona is $20.01, according to ZipRecruiter salary data. Most workers in this role earn between $16.11 and $22.40 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 Arizona?

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

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

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

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

Cities in Arizona 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 Arizona as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 14% Part Time, 2% Temporary, and 6% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $41,626 per year, or $20 per hour.

QA/QC Engineer I

Hanger, Inc.

Phoenix, AZ

$27.02 - $40.48/hr

Full-time

Posted 14 days ago

Job description

Overview

The Quality Assurance Engineer I supports quality assurance and product development activities in accordance with medical device regulations, including 21 CFR 820, the Medical Device Directive (MDD), ISO 13485, and ISO 14971. Under the guidance of senior QA staff, the engineer assists with incoming inspection and product release tasks by following established procedures to help ensure products meet defined specifications and quality requirements. The duties will also include providing support for document control activities, helping maintain quality records, assisting with CAPA documentation, and participating in basic product review investigations as assigned. The QA Engineer I also works with Product Development by completing required design control documentation and following established processes for new and existing product lines.


Responsibilities

  • Support QA/QC activities by following established procedures and requirements related to 21 CFR 820, ISO standards, and CE mark guidelines under the direction of senior team members.
  • Perform basic incoming inspections and final product checks using predefined inspection criteria and document results accurately.
  • Assist with complaint intake activities by logging complaints, organizing required documentation, and escalating issues to senior QA staff for evaluation in accordance with regulatory procedures.
  • Provide support for document control tasks, including updating logs, routing documents for approval, and maintaining organized and compliant document files.
  • Help maintain quality records, such as device history records, QA logs, test reports, and equipment records, ensuring files are complete and properly stored.
  • Assist in tracking product traceability data by entering information into tracking systems and verifying completeness.
  • Participate in validation activities (IQ, OQ, PQ) by collecting data, preparing documentation, and performing routine test steps under supervision.
  • Support calibration and equipment maintenance programs by scheduling calibration service, maintaining calibration logs, and helping track equipment status.

Qualifications

Minimum:

  • Bachelor’s degree in electrical or mechanical engineering 

Preferred:

  • Some experience in the medical device industry, quality assurance, regulatory affairs, or a related engineering environment; exposure to products with electronic components is preferred.
  • Familiarity with basic quality and regulatory concepts such as 21 CFR 820, 21 CFR Part 11, and ISO 13485; coursework, project work, or prior internship experience in these areas is preferred.
  • Experience supporting CAPA‑related activities (e.g., gathering data, documenting actions, assisting with investigations) within a structured quality system is beneficial.