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Medical Device Qa Jobs in Arizona (NOW HIRING)

Hanger, Inc.

QA/QC Engineer I

Phoenix, AZ

$27.02 - $40.48/hr

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 ...

Hanger

QA/QC Engineer I

Phoenix, AZ · On-site

$60 - $80/hr

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 ...

Hanger, Inc.

QA/QC Engineer I

Phoenix, AZ · On-site

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 ...

Hanger, Inc.

QA/QC Engineer I

Phoenix, AZ · On-site

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 ...

Dexcom

Sr Software QA Engineer

Mesa, AZ

Demonstrated knowledge of medical device quality systems and regulatory requirements, including FDA 21 CFR Part 820, IEC 62304, ISO 13485, ISO 14971, IEC 82304, EU MDR, and other applicable global ...

GN Group

Medical Device Sales

Prescott, AZ · On-site

$80 - $100/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 ...

Gn

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 ...

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 ...

Ralliant

Quality Assurance Engineer

Chandler, AZ · On-site

Quality Assurance Engineer Job Overview PacSci EMC is seeking a Quality Assurance Engineer to ... Experience in other highly regulated manufacturing environments, particularly medical device or ...

onsemi

Sr. Customer Quality Manager

Scottsdale, AZ · On-site

$150 - $200/hr

The position will require a strong medical device as well as semiconductor quality background, as daily collaboration with Sales, Product & Test Engineering, Product Quality, Central Engineering ...

DHL

Quality Assurance Supervisor

Waddell, AZ · On-site

$55K - $90K/yr

DHL Supply Chain offers multiple benefits including Medical, Dental, Vision, Prescription, Discounted Stock Purchase, and a generous PTO policy. Quality Assurance Supervisor (US-N) Would you like to ...

DPDHL

Quality Assurance Supervisor

Waddell, AZ

$55K - $90K/yr

DHL Supply Chain offers multiple benefits including Medical, Dental, Vision, Prescription, Discounted Stock Purchase, and a generous PTO policy. Quality Assurance Supervisor (US-N) Would you like to ...

DHL

Quality Assurance Supervisor

Goodyear, AZ · On-site

$55K - $90K/yr

DHL Supply Chain offers multiple benefits including Medical, Dental, Vision, Prescription, Discounted Stock Purchase, and a generous PTO policy. Quality Assurance Supervisor (US-N) Would you like to ...

DPDHL

Quality Assurance Supervisor

Goodyear, AZ · On-site

$55K - $90K/yr

DHL Supply Chain offers multiple benefits including Medical, Dental, Vision, Prescription, Discounted Stock Purchase, and a generous PTO policy. Quality Assurance Supervisor (US-N) Would you like to ...

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All JobsMedical Device Qa JobsMedical Device Qa Jobs in Arizona

Medical Device Qa information

See Arizona salary details

$12

$35

$68

How much do medical device qa jobs pay per hour?

As of Sep 8, 2026, the average hourly pay for medical device qa in Arizona is $35.72, according to ZipRecruiter salary data. Most workers in this role earn between $17.74 and $48.54 per hour, depending on experience, location, and employer.

What is a medical device QA?

Medical Device Quality Assurance (QA) professionals are responsible for ensuring that medical devices meet regulatory standards and are safe and effective for use. They develop and implement quality management systems, conduct audits, and oversee documentation throughout the product lifecycle. QA professionals also work closely with engineering, manufacturing, and regulatory teams to identify and resolve quality issues, manage risk, and ensure compliance with industry standards such as ISO 13485 and FDA regulations.

What are the key skills and qualifications needed to thrive as a medical device QA, and why are they important?

To thrive as a Medical Device QA, you need a solid understanding of quality assurance principles, regulatory standards (such as ISO 13485 and FDA 21 CFR Part 820), and a relevant degree in engineering or life sciences. Familiarity with quality management systems (QMS), document control software, and auditing tools is typically required, along with certifications like Certified Quality Auditor (CQA) or Six Sigma. Strong attention to detail, problem-solving abilities, and effective communication help ensure compliance and drive continuous improvement. These skills and qualities are crucial to maintaining product safety, regulatory compliance, and overall quality within the highly regulated medical device industry.

What are some common challenges faced by medical device QA professionals, and how can they be addressed?

Medical Device QA professionals often encounter challenges such as navigating complex regulatory requirements, ensuring product consistency, and keeping up with frequent changes in standards. Addressing these challenges typically involves staying current with FDA and ISO updates, maintaining robust documentation practices, and fostering clear communication with cross-functional teams like R&D and manufacturing. Regular training sessions and proactive risk management strategies also help QA professionals ensure quality and compliance throughout the product lifecycle.

What is the difference between Medical Device Qa vs Medical Device Quality Inspector?

AspectMedical Device QaMedical Device Quality Inspector
CertificationsISO 13485, FDA regulations, Six SigmaISO 13485, FDA regulations, Six Sigma
Work EnvironmentDesign, development, and process oversight in manufacturingInspection and testing on production lines
ResponsibilitiesEnsuring quality systems and complianceInspecting products for defects and conformance

Medical Device Qa professionals focus on quality assurance processes, compliance, and system improvements, while Medical Device Quality Inspectors primarily perform product inspections and defect detection. Both roles require similar certifications and work within the medical device industry, but their daily tasks and focus areas differ significantly.

What are popular job titles related to Medical Device Qa jobs in Arizona?

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

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

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

Medical Device Qa jobs near you
Infographic showing various Medical Device Qa 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 $74,292 per year, or $35.7 per hour.

QA/QC Engineer I

Hanger, Inc.

Phoenix, AZ

$27.02 - $40.48/hr

Full-time

Posted 17 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.