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Medical Device Qa Jobs in Arizona (NOW HIRING)

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 ...

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 ...

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 ...

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Medical Device Assembler

Marana, AZ · On-site

$17 - $18.08/hr

Medical Device Assembler Location: Marana, AZ 85653 Employment Type: W2 Contract - 12 Months with ... Perform required transactions within quality systems to support manufacturing and quality ...

Medical Device Assembler

Marana, AZ · On-site

$17.08 - $18.08/hr

Medical Device Assembler Location: Marana, AZ 85653 Employment Type: W2 Contract - 12 Months with ... Perform required transactions within quality systems to support manufacturing and quality ...

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 ...

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 ...

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 ...

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 ...

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 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 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 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 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 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 ...

Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical ... Job Title Director Quality Assurance The Opportunity The Director Quality Assurance is responsible ...

Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical ... Job Title Director Quality Assurance The Opportunity The Director Quality Assurance is responsible ...

Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical ... Job Title Director Quality Assurance The Opportunity The Director Quality Assurance is responsible ...

Position Summary The Quality Assurance Supervisor ensures the timely and effective implementation ... Medical (full-time only) * Dental (full-time only) * Vision (full-time only) * 401(k) with Company ...

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Showing results 1-20

Medical Device Qa information

See Arizona salary details

$12

$35

$68

How much do medical device qa jobs pay per hour?

As of Sep 2, 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.

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 • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 12 days ago


Job description

Why Us?
With a mantra of Empowering Human Potential, Hanger, Inc. is the world's premier provider of orthotic and prosthetic (O&P) services and products, offering the most advanced O&P solutions, clinically differentiated programs and unsurpassed customer service. Hanger's Patient Care segment is the largest owner and operator of O&P patient care clinics nationwide. Through its Products & Services segment, Hanger distributes branded and private label O&P devices, products and components, and provides rehabilitative solutions to the broader market. With 160 years of clinical excellence and innovation, Hanger's vision is to lead the orthotic and prosthetic markets by providing superior patient care, outcomes, services and value. Collectively, Hanger employees touch thousands of lives each day, helping people achieve new levels of mobility and freedom.
Could This Be For You?
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.
Your Impact
  • 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.

Minimum 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.

Additional Success Factors
  • Ability to work and interact with internal and external parties including internal customers, distributors, suppliers.
  • Ability to work in multi-tasked environment with deadlines.
  • Strong ability to work independently on multiple time sensitive projects.
  • Strong written and oral communication skills.
  • Basic knowledge of medical device development and commercialization
  • Understanding of electronic assembly and component manufacturing processes.
  • Act with integrity in all ways and at all times, remaining honest, transparent, and respectful in all relationships.
  • Keep the patient at the center of everything that you do, building lifelong trust.
  • Foster open collaboration and constructive dialogue with everyone around you.
  • Continuously innovate new solutions, influencing and responding to change.
  • Focus on superior outcomes, and calibrate work processes for outstanding results.

Our Investment in You
  • Competitive Compensation Packages
  • 8 Paid National Holidays & 4 additional Floating Holidays
  • PTO that includes Vacation and Sick time
  • Medical, Dental, and Vision Benefits
  • 401k Savings and Retirement Plan
  • Paid Parental Bonding Leave for New Parents
  • Flexible Work Schedules and Part-time Opportunities
  • Generous Employee Referral Bonus Program
  • Mentorship Programs- Mentor and Mentee
  • Student Loan Repayment Assistance by Location
  • Relocation Assistance
  • Regional & National traveling CPO/CO/CP opportunities
  • Volunteering for Local and National events such as Hanger's BAKA Bootcamp and EmpowerFest

Hanger, Inc. is committed to providing equal employment opportunity in all aspects of the employer-employee relationship. All conditions and privileges of employment are administered to all employees without discrimination or harassment because of race, religious creed, color, age, sex, sexual orientation, gender identity, national origin, religion, marital status, medical condition, physical or mental disability, military service, pregnancy, childbirth and related medical conditions, special disabled veteran status, or any other classification protected by federal, state, and local laws and ordinances. The company will comply with all applicable state or local fair employment laws that forbid discrimination or harassment on the basis of other protected characteristics. Retaliation against any employee for filing or supporting a complaint of discrimination or harassment is prohibited.
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