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Contract Quality Engineer Medical Device Jobs in Phoenix, AZ

Aequor Technologies

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 ...

Aequor Inc

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 ...

millenniumsoft

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 ...

Aptyx

Quality Manager- MED DEVICE ISO13485

Tempe, AZ · On-site

... medical injection molding facility undergoing product and equipment transfers and eventual site ... The Quality Manager will lead a team of quality engineers and inspectors, partner closely with ...

Kelly

Be Seen First

Medical Device Assembler

Phoenix, AZ · On-site

$19/hr

Collaborate with engineers, supervisors, and team leads to improve quality and process efficiency ... Microchip, Semiconductor, and/or Medical Device experience. * Clean room or controlled environment ...

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Contract Quality Engineer Medical Device information

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$44.7K

$83.4K

$118.2K

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

As of May 28, 2026, the average yearly pay for contract quality engineer medical device in Phoenix, AZ is $83,443.00, according to ZipRecruiter salary data. Most workers in this role earn between $71,500.00 and $92,300.00 per year, depending on experience, location, and employer.

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

To thrive as a Contract Quality Engineer in the Medical Device field, you need expertise in quality assurance, regulatory compliance (such as ISO 13485 and FDA regulations), and a background in engineering or life sciences. Familiarity with tools like CAPA systems, risk management software, and proficiency in quality management systems (QMS) is typically required. Strong analytical thinking, attention to detail, and effective communication skills set top performers apart in this role. These skills are essential to ensure product safety, regulatory compliance, and the successful launch and maintenance of medical devices in a highly regulated environment.

How does a Contract Quality Engineer in the medical device industry typically collaborate with cross-functional teams?

As a Contract Quality Engineer in the medical device sector, you will frequently work closely with cross-functional teams, including R&D, manufacturing, regulatory affairs, and supply chain. Your responsibilities often involve reviewing design documentation, participating in risk assessments, and ensuring production processes meet both internal quality standards and regulatory requirements. Effective communication is key, as you'll be responsible for conveying quality expectations, addressing non-conformities, and supporting project timelines. This collaborative environment provides valuable experience in coordinating with diverse professionals while upholding strict industry standards.

What does a Contract Quality Engineer do in the medical device industry?

A Contract Quality Engineer in the medical device industry is responsible for ensuring that products meet regulatory and company quality standards during a specific project or timeframe. They typically work on a contract basis, focusing on tasks like process validation, risk management, root cause analysis, and compliance with standards such as ISO 13485 and FDA regulations. Their role often involves collaborating with engineering, production, and regulatory teams to troubleshoot quality issues and implement corrective actions. They play a key role in maintaining product safety and regulatory compliance throughout the manufacturing process.

What is the difference between Contract Quality Engineer Medical Device vs Contract Quality Engineer Pharmaceutical?

AspectContract Quality Engineer Medical DeviceContract Quality Engineer Pharmaceutical
CertificationsISO 13485, FDA QSR, GMPICH Q7, GMP, FDA regulations
Work EnvironmentMedical device manufacturing, labs, compliance auditsPharmaceutical production, labs, quality assurance
Industry UsageMedical device companies, OEMs, suppliersPharmaceutical firms, biotech companies, contract manufacturers

Both roles focus on quality assurance and regulatory compliance but differ mainly in industry-specific standards and environments. Contract Quality Engineers Medical Device work primarily with ISO 13485 and FDA QSR standards in device manufacturing, while Contract Quality Engineers Pharmaceutical focus on GMP and ICH Q7 regulations in drug production. Understanding these differences helps candidates target the right industry and certifications for their career goals.

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 Contract Quality Engineer Medical Device jobs in Phoenix, AZ? For Contract Quality Engineer Medical Device jobs in Phoenix, AZ, the most frequently searched job titles are:
What job categories do people searching Contract Quality Engineer Medical Device jobs in Phoenix, AZ look for? The top searched job categories for Contract Quality Engineer Medical Device jobs in Phoenix, AZ are:
Contract Quality Engineer Medical Device jobs near you
Infographic showing various Contract Quality Engineer Medical Device job openings in Phoenix, AZ as of May 2026, with employment types broken down into 5% As Needed, 68% Full Time, 5% Part Time, 1% Temporary, and 21% Contract. Highlights an 92% Physical, 1% Hybrid, and 7% Remote job distribution, with an average salary of $83,443 per year, or $40.1 per hour.
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

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