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Medical Device Qa Jobs in Arizona (NOW HIRING)

Regulated QA Req Id: 2080 State/Province: Arizona Business: Gore Medical Products Category: Supply ... Demonstrated working knowledge of FDA medical device quality system regulations and ISO medical ...

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 ...

You will have experience with nonconforming material handling and familiarity with medical device Quality Systems Regulations 21CFR Part 820. * You take initiative to coordinate Quality Assurance ...

You will have experience with nonconforming material handling and familiarity with medical device Quality Systems Regulations 21CFR Part 820. * You take initiative to coordinate Quality Assurance ...

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 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 ...

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Medical Device Qa information

See Arizona salary details

$12

$35

$68

How much do medical device qa jobs pay per hour?

As of Aug 28, 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 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:

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.

Full-time

Posted 12 days ago


W. L. Gore & Associates rating

8.9

Company rating: 8.9 out of 10

Based on 80 frontline employees who took The Breakroom Quiz

8th of 544 rated manufacturers


Job description

Regulated QA
Req Id: 2080
State/Province: Arizona
Business: Gore Medical Products
Category: Supply Chain
Sub-Category: Quality
Work Arrangement: Hybrid
Posting Start Date: 8/13/26
Posting End Date: 8/28/26
About the Role
We are looking for a Quality Assurance Professional to join the Gore Medical Quality Assurance team. In this role, you will work with cross-functional teams to support day-to-day manufacturing and plant operations, including executing the NCR, CAPA, Change Management, and other quality system processes, addressing product issues, defining and implementing effective corrective actions, and monitoring post-implementation effectiveness.
This position will be located at our facility in Phoenix, Arizona, with the possibility of a hybrid work arrangement.
Responsibilities
  • Support the day to day manufacturing process including problem solving, CAPA and nonconformance investigations and partner cross-functionally on appropriate risk-based decision making
  • Coordinate and support execution of the nonconforming product (NCR) and corrective and preventive actions (CAPA) processes
  • Ensure constant audit readiness for product lines supported and assist in audit preparation and coordination to deliver successful audit results
  • Work and communicate with the quality assurance and cross functional teams as well as support organizations across the product lines and Gore Medical to support a quick and robust decision-making process in support of quality system requirements
  • Support prioritized activities, including NCR, CAPA, Change Management, FIR and operational improvements
  • Guide the manufacturing team through resolution of daily issues related to quality system requirements and execution of the quality system
  • Train and educate others on quality system requirements and good documentation practices to ensure compliance
  • Participate in and perform quality system compliance audits
  • If needed, coordinate the product failure investigation process (FIR) from initiation to completion to ensure time-sensitive activities, documentation and approvals are complete
  • Enhance quality systems (including software implementation and validation)

Required Qualifications
  • Minimum of 4 years of Quality Assurance or other quality related experience in a medical-device, pharmaceutical, biotech or other regulated industry
  • Demonstrated working knowledge of FDA medical device quality system regulations and ISO medical device industry standards
  • Excellent written and oral communication skills
  • Strong interpersonal and influencing skills
  • Conflict resolution skills
  • Ability to work independently, as well as part of a diverse team
  • Ability to set and meet aggressive timelines
  • Ability to travel up to 5%

Desired Qualifications
  • Bachelor's degree in an applicable science or engineering field, OR a 2-year degree plus 2 or more years of medical device experience in a manufacturing or operations role
  • Experience supporting various manufacturing processes
  • ISO 13485 Lead Auditor Certification
  • Strong knowledge of ERP and PLM systems

This position offers a hybrid work arrangement in the country from which the Associate is employed. Eligibility is dependent on the responsibilities of the role and business needs, and the Associate must agree to comply with Gore's work arrangement policies.
What We Offer
Our success is based on the capability and creativity of our Associates, and we are proud to offer a comprehensive and competitive total rewards program that supports your everyday and helps you build your tomorrow.
We provide benefits that offer choice and flexibility and promote overall well-being. And in keeping with our belief that every Associate should share in the collective success of the enterprise; we provide a distinctive Associate Stock Ownership Plan in each country as well as potential opportunities for "profit-sharing". Learn more at gore.com/careers/benefits
Gore is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender, national origin, ancestry, age, status as a qualified individual with a disability, genetic information, pregnancy status, medical condition, marital status, sexual orientation, status as a protected veteran, gender identity and expression, and any other characteristic protected by applicable laws and regulations.
Gore is committed to a drug-free workplace. All employment is contingent upon successful completion of drug and background screening. Gore will consider qualified applicants with criminal histories, e.g., arrest and conviction records, in a manner consistent with the requirements of applicable laws.
Gore requires all applicants to be eligible to work within the United States. Gore generally will not sponsor visas unless otherwise noted on the position description.
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