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Senior Quality Engineer Medical Device Jobs in Phoenix, AZ

Quality Engineer (MED DEVICE)

Tempe, AZ · On-site

$70.10K - $90.50K/yr

Quality Engineer (MED DEVICE) The Quality Engineer in Medical Plastic Injection Molding is responsible for overseeing and ensuring the quality of existing and new products and processes within the ...

Quality Engineer (MED DEVICE)

Tempe, AZ · On-site

$70.10K - $90.50K/yr

Quality Engineer (MED DEVICE) The Quality Engineer in Medical Plastic Injection Molding is responsible for overseeing and ensuring the quality of existing and new products and processes within the ...

Sr. Quality Assurance Engineer

Phoenix, AZ · On-site

$87.90K - $119.10K/yr

The Sr. Quality Engineer has sole responsibility for the planning, implementation, and ... Comprehensive insurance coverage including medical, dental, vision, life, disability, Employee ...

Sr. Quality Assurance Engineer

Phoenix, AZ · On-site

$87.90K - $119.10K/yr

The Sr. Quality Engineer has sole responsibility for the planning, implementation, and ... Comprehensive insurance coverage including medical, dental, vision, life, disability, Employee ...

Senior Quality Engineer

Phoenix, AZ · On-site

$45 - $50/hr

Description The Senior Quality Engineer - Document Management Platform is responsible for defining ... If eligible, the benefits available for this temporary role may include the following: • Medical ...

Senior Quality Engineer

Phoenix, AZ · On-site

$50 - $55/hr

Description The Senior Quality Engineer - Document Management Platform is responsible for defining ... If eligible, the benefits available for this temporary role may include the following: • Medical ...

Senior Quality Engineer

Mesa, AZ · On-site

$87.80K - $119.10K/yr

The Senior Quality Engineer serves as a technical and systems steward for site quality processes and business systems. This role provides senior-level quality leadership without direct people ...

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Sr. Quality Engineer (Manufacturing)

Mesa, AZ · On-site

$87.80K - $119.10K/yr

The Senior Quality Engineer serves as a technical and systems steward for site quality processes ... medical, military and defense, industrial, quantum computing, radars, railway, space, test and ...

Senior Quality Engineer

Chandler, AZ · On-site

$87.20K - $118.20K/yr

Your role The Quality Engineer supports the maintained compliancy within their STC to ISO9001:2015. ISO14001, ISO45001 (or local equivalent) and Vacuum Technique Quality standards at all times. The ...

Sr. Quality Engineer

Tempe, AZ · On-site

$86K - $116.60K/yr

Bachelor's degree in engineering, biology, biomedical technology, chemistry, or electronics. * 5+ years' experience in quality engineering with medical devices; strong preference for experience ...

Senior Quality Engineer

Chandler, AZ · On-site

$90.40K - $122.50K/yr

Your role The Quality Engineer supports the maintained compliancy within their STC to ISO9001:2015. ISO14001, ISO45001 (or local equivalent) and Vacuum Technique Quality standards at all times. The ...

Senior Quality Engineer

Chandler, AZ · On-site

$87.20K - $118.20K/yr

Your role The Quality Engineer supports the maintained compliancy within their STC to ISO9001:2015. ISO14001, ISO45001 (or local equivalent) and Vacuum Technique Quality standards at all times. The ...

Senior QA Engineer - Supplier Quality

Mesa, AZ · On-site

$87.80K - $119.10K/yr

The Senior level Supplier Quality Engineer engages suppliers in three fundamental means: * Supplier ... You have previous medical device experience in quality engineering or supplier quality. * You are ...

Senior QA Engineer - Supplier Quality

Mesa, AZ

$87.80K - $119.10K/yr

The Senior level Supplier Quality Engineer engages suppliers in three fundamental means: * Supplier ... You have previous medical device experience in quality engineering or supplier quality. * You are ...

Quality Engineer

Tempe, AZ · On-site

$69K - $89.10K/yr

Medical Device Company Job Category: Engineering Level Of Experience: Mid-Level Employment Type: Contract on W2 (Need US Citizens Or GC Holders Only) * Responsible for reviewing and assessing Quality ...

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Senior Quality Engineer Medical Device information

See Phoenix, AZ salary details

$60.1K

$104.5K

$145.5K

How much do senior quality engineer medical device jobs pay per year?

As of May 28, 2026, the average yearly pay for senior quality engineer medical device in Phoenix, AZ is $104,546.00, according to ZipRecruiter salary data. Most workers in this role earn between $87,900.00 and $119,100.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Senior Quality Engineer in Medical Devices, and why are they important?

To excel as a Senior Quality Engineer in Medical Devices, you need a solid background in engineering, quality assurance, and regulatory compliance, typically with a relevant degree and experience in the medical device industry. Familiarity with ISO 13485, FDA 21 CFR Part 820, risk management tools (such as FMEA), and quality management systems is crucial, and certifications like CQE or Six Sigma are often preferred. Strong problem-solving, attention to detail, and effective communication skills distinguish top performers in this role. These competencies ensure product safety, regulatory compliance, and the continuous improvement of processes critical to patient outcomes and company success.

How does a Senior Quality Engineer in the medical device industry typically collaborate with cross-functional teams during product development?

As a Senior Quality Engineer in the medical device sector, you will work closely with cross-functional teams including R&D, manufacturing, regulatory affairs, and supply chain. Your role involves ensuring quality standards are integrated throughout the product lifecycle, from design reviews and risk assessments to process validation and compliance documentation. Regular meetings, joint problem-solving sessions, and clear communication are vital to resolve issues efficiently and maintain regulatory compliance. This collaborative environment helps to ensure both product safety and timely market release.

What are Senior Quality Engineers in the medical device industry?

Senior Quality Engineers in the medical device industry are professionals responsible for ensuring that medical devices meet regulatory standards and quality requirements throughout their lifecycle. They lead quality assurance activities, develop and implement testing protocols, coordinate with design and manufacturing teams, and help ensure compliance with relevant regulations such as FDA and ISO standards. Their expertise ensures that products are safe, effective, and reliable for patient use. They also mentor junior engineers and may play a key role in audits and process improvements.

What is the difference between Senior Quality Engineer Medical Device vs Quality Engineer Medical Device?

AspectSenior Quality Engineer Medical DeviceQuality Engineer Medical Device
ResponsibilitiesLead quality initiatives, oversee audits, mentor team membersAssist in quality processes, support audits, perform inspections
Experience & CertificationsTypically 5+ years, often ISO 13485, FDA regulationsEntry to mid-level, basic knowledge of industry standards
Work EnvironmentLeadership roles, cross-functional teams, strategic planningOperational tasks, documentation, compliance support
Usage & IndustryCommonly used in manufacturing, R&D, and quality departmentsUsed across similar settings, often as a stepping stone role

The main difference between a Senior Quality Engineer Medical Device and a Quality Engineer Medical Device lies in experience, responsibilities, and leadership scope. Senior roles involve strategic oversight and mentorship, while standard Quality Engineers focus on supporting quality processes and compliance tasks.

What are the most commonly searched types of Quality Engineer Medical Device jobs in Phoenix, AZ? The most popular types of Quality Engineer Medical Device jobs in Phoenix, AZ are:
What are popular job titles related to Senior Quality Engineer Medical Device jobs in Phoenix, AZ? For Senior Quality Engineer Medical Device jobs in Phoenix, AZ, the most frequently searched job titles are:
What job categories do people searching Senior Quality Engineer Medical Device jobs in Phoenix, AZ look for? The top searched job categories for Senior Quality Engineer Medical Device jobs in Phoenix, AZ are:
What cities near Phoenix, AZ are hiring for Senior Quality Engineer Medical Device jobs? Cities near Phoenix, AZ with the most Senior Quality Engineer Medical Device job openings:
Quality Engineer (MED DEVICE)

Quality Engineer (MED DEVICE)

Aequor Technologies

Tempe, AZ • On-site

$70.10K - $90.50K/yr

Full-time

This job post has expired today. Applications are no longer accepted.


Job description

Quality Engineer (MED DEVICE)
The Quality Engineer in Medical Plastic Injection Molding is responsible for overseeing and ensuring the quality of existing and new products and processes within the medical device manufacturing environment. This role involves implementing quality assurance practices, measurement of product utilizing CMM, ensuring compliance with regulatory standards, conducting audits, and driving continuous improvement initiatives.
Key Responsibilities:
  • Quality Assurance:
  • Develop, implement, and maintain quality assurance policies and procedures to ensure product quality and compliance.
  • Create and maintain Quality Assurance documentation including Control Plans, pFMEAs, Quality Alerts, and Inspection Plans.
  • Conduct Process Validations for new and revised products and processes ensuring long term capability.
  • Monitor production processes to ensure consistent product quality.
  • Collect and analyze data on product quality and process performance.
  • Quality Control:
  • Conduct audits of raw materials, in-process products, and finished goods to verify adherence to quality standards.
  • Measure parts using hand gages, CMM, Video Measurement System.
  • Ability to interpret part prints. Utilize GD&T when applicable.
  • Regulatory Compliance:
  • Ensure that all products and processes comply with relevant medical device regulations and standards, such as ISO 13485 and FDA requirements.
  • Prepare and manage documentation for regulatory submissions and audits.
  • Problem Solving and Root Cause Analysis:
  • Lead root cause analysis and corrective action activities for non-conforming products.
  • Collaborate with production, engineering, and R&D teams to implement effective corrective and preventive actions.
  • Customer Interaction:
  • Address customer complaints and quality concerns including processing of Return Material Authorization, RMA, and formal Corrective Actions.
  • Support customer audits and visits by providing necessary documentation and information.
  • Support and provide routine status updates to Customers regarding open actions including, but not limited to, Corrective Actions, Projects, and/or other Status Updates.
  • Active participant in Drawing Reviews to ensure that Quality Requirements can be satisfied.
  • Support Quality requirements for New Product Introduction working closely with Program Managers to support critical timelines for completion.
  • Continuous Improvement:
  • Drive continuous improvement initiatives aimed at enhancing product quality, reducing waste, and improving efficiency. Provide review of any changes for impact on QMS.
  • Identify areas for process improvement and lead initiatives to enhance product quality and manufacturing efficiency.
  • Participate in and lead cross-functional quality improvement teams.
  • Training and Development:
  • Mentor and train quality control personnel and junior quality engineers.
  • Conduct quality-related training programs for manufacturing and other relevant staff.
  • Auditing and Compliance:
  • Conduct internal audits to ensure compliance with quality management systems and regulatory requirements.
  • Prepare for and support external audits by regulatory bodies and customers.

Qualifications:
  • Education: Bachelor's degree in Engineering, preferably in Mechanical, Industrial, or Plastics Engineering.
  • Experience: Minimum of 3-5 years of experience in a quality role within the medical device manufacturing industry, with significant experience in plastic injection molding.
  • Knowledge:
    • In-depth understanding of quality assurance principles and methodologies.
    • Extensive knowledge of injection molding processes and equipment.
    • Familiarity with medical device regulations and standards, including ISO 13485 and FDA requirements.
    • Experience working with CMMs to measure parts. Some programming experience preferred but will train if needed.
  • Skills:
    • Strong analytical and problem-solving skills.
    • Excellent attention to detail and organizational skills.
    • Proficiency in statistical analysis and quality management software.
    • Effective communication and leadership skills.
  • Certifications: Certification such as Certified Quality Engineer (CQE) from ASQ is highly desirable.

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About Aequor Technologies

Sourced by ZipRecruiter

Aequor Technologies, located in Piscataway, New Jersey, is an established IT consulting and solutions company that operates primarily in the United States. The company, founded in 1998, specializes in providing high-value, cost-effective IT services and solutions for a variety of industries, including health care, life sciences, manufacturing, and media and entertainment. They offer a wide array of services including IT consulting, application development, infrastructure management, and strategic staffing solutions. Its mission is to facilitate its clients in their pursuit of achieving business objectives through effective and efficient use of technology. Aequor Technologies is a significant player in its field, boasting several accomplishments including repeated recognition as one of the fastest growing privately-held companies in the U.S. by Inc. 5000.

Industry

Recruiting and staffing services

Company size

201 - 500 Employees

Headquarters location

Piscataway, NJ, US

Year founded

1998