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Quality Engineer Medical Devices Jobs in Virginia

Quality Engineer

Alexandria, VA · On-site

$77K - $99K/yr

Overview As the Quality Engineer at MPR, you play a key role in ensuring the MPR quality assurance ... and medical devices. You'll serve as an internal QA resource ensuring our deliverables meet ...

... medical devices on the European market ... This position applies a mix of engineering and design knowledge, newfound regulatory expertise ...

Be Seen First

We are seeking a Quality Manufacturing Engineer extensive experience in Medical Devices to oversee Manufacturing Quality projects and line transfers for a Medical Device company. The perfect ...

Be Seen First

We are seeking a Quality Manufacturing Engineer extensive experience in Medical Devices to oversee Manufacturing Quality projects and line transfers for a Medical Device company. The perfect ...

... medical devices on the European market ... This position applies a mix of engineering and design knowledge, newfound regulatory expertise ...

Quality Engineer

Roanoke, VA · On-site

$70K - $91K/yr

The Production Quality Engineer takes on a significant role ensuring the quality of products meet both internal standards and customer expectations. Through implementing and monitoring quality rules ...

Quality Engineer (Video)

Tysons Corner, VA · On-site

$72K - $93K/yr

Good understanding of computer networking and ability to troubleshoot malfunctioning devices ... The package includes medical plans with company subsidies, a Health Savings Account (HSA) with a ...

Quality Engineer

Roanoke, VA · On-site

$55K - $85K/yr

Description The Production Quality Engineer takes on a significant role ensuring the quality of products meet both internal standards and customer expectations. Through implementing and monitoring ...

Quality Engineer

Wallops Island, VA · On-site

$71K - $92K/yr

Quality Engineer BELONG. CONNECT. GROW. with KBR. Around here, we define the future. We are a ... with company match, medical, dental, vision, life insurance, AD&D, flexible spending account ...

Quality Engineer

Richmond, VA · On-site

$90 - $120/hr

Quality Engineer Hyper Solutions Inc Richmond, Other / Non-US, United States About this position ... In addition to competitive compensation and comprehensive benefits, including employer-paid medical ...

Quality Engineer

Lynchburg, VA · On-site

$85 - $105/hr

What You'll Do As a Quality Engineer, you'll lead technical problem-solving activities, drive ... medical * dental * vision coverage * retirement savings programs * paid time off * life and ...

Quality Engineer

Chesapeake, VA · On-site

$87K - $109K/yr

The Quality Engineer plays a critical role in ensuring the highest standards of quality across our ... includes medical, dental, vision, EAP, tuition reimbursement, Legal Plan, 401K, PTO, and more!

Quality Engineer

Virginia Beach, VA · On-site

$70 - $110/hr

Quality Engineer Full-time Regular 4484- Plastics Mfg Virginia Beach, VA, US 9 days ago Requisition ID: 1600 Salary Range: $70,000.00 To $110,000.00 Annually Who We Are : IMS Gear is a global ...

Quality Engineer

Lynchburg, VA · On-site

$86K - $93K/yr

What You'll Do As a Quality Engineer, you'll lead technical problem-solving activities, drive ... Eligible employees have access to medical, dental, and vision coverage, retirement savings programs ...

Quality Engineer

Richmond, VA · On-site

$90K - $120K/yr

The Quality Engineer at Hyper Solutions is responsible for ensuring that product quality ... In addition to competitive compensation and comprehensive benefits, including employer-paid medical ...

Quality Engineer

Daleville, VA · On-site

$56K - $95K/yr

Compensation Range: $56,800 - $95,800 Quality Engineer Daleville, VA | 🏢 Munters Corporation Join a global leader in climate solutions. At Munters, we develop innovative, energy-efficient systems ...

Quality Engineer

Lynchburg, VA · On-site

$65 - $95/hr

Overview Quality Engineer acts as the Voice of the Customer and is responsible for ensuring that ... Medical Components ISO 13485; Aerospace AS9100; Consumer Products ISO 9001. This role must comply ...

Quality Engineer

Daleville, VA · On-site

$56K - $95K/yr

Compensation Range: $56,800 - $95,800 Quality Engineer Daleville, VA | Munters Corporation Join a global leader in climate solutions. At Munters, we develop innovative, energy-efficient systems for ...

Quality Engineer

Richmond, VA · On-site

$90K - $120K/yr

The Quality Engineer at Hyper Solutions is responsible for ensuring that product quality ... In addition to competitive compensation and comprehensive benefits, including employer-paid medical ...

Compensation Range: $56,800 - $95,800 Quality Engineer Daleville, VA | 🏢 Munters Corporation Join a global leader in climate solutions. At Munters, we develop innovative, energy-efficient systems ...

Showing results 21-40

Quality Engineer Medical Devices information

See Virginia salary details

$44.6K

$83.3K

$118K

How much do quality engineer medical devices jobs pay per year?

As of Sep 4, 2026, the average yearly pay for quality engineer medical devices in Virginia is $83,318.00, according to ZipRecruiter salary data. Most workers in this role earn between $71,400.00 and $92,200.00 per year, depending on experience, location, and employer.

What does a quality engineer do in the medical device industry?

A Quality Engineer in the medical device industry is responsible for ensuring that products meet regulatory standards and quality requirements throughout their lifecycle. They develop and implement quality control processes, conduct risk assessments, lead investigations into product defects, and work closely with cross-functional teams to ensure compliance with regulations such as FDA and ISO 13485. Their work helps to guarantee the safety, reliability, and effectiveness of medical devices before they reach patients.

How does a quality engineer collaborate with cross-functional teams in the medical device industry?

Quality Engineers in the medical device field work closely with design, manufacturing, and regulatory teams to ensure products meet stringent quality and compliance standards. They participate in design reviews, help develop verification and validation protocols, and support the implementation of corrective actions. Regular communication with production and R&D teams is essential to identify potential risks early and to ensure that quality is built into every stage of product development. This collaborative approach not only improves product safety and efficacy but also streamlines regulatory submissions and audits.

What are the key skills and qualifications needed to thrive as a quality engineer in medical devices, and why are they important?

To thrive as a Quality Engineer in Medical Devices, you typically need a degree in engineering or a related field, combined with knowledge of quality assurance principles and regulatory requirements (such as ISO 13485 and FDA regulations). Familiarity with risk management tools, validation protocols, and quality management systems (QMS), as well as certifications like CQE (Certified Quality Engineer), are highly valuable. Strong analytical thinking, attention to detail, and effective communication skills enable you to identify issues, collaborate with cross-functional teams, and ensure compliance. These competencies are crucial for maintaining product safety, meeting regulatory standards, and supporting a culture of continuous improvement in the medical device industry.

What is the difference between Quality Engineer Medical Devices vs Quality Technician Medical Devices?

AspectQuality Engineer Medical DevicesQuality Technician Medical Devices
CertificationsISO 13485, Six Sigma, ASQ certificationsISO 13485, basic quality certifications
ResponsibilitiesDesigning quality systems, process improvements, root cause analysisInspecting products, conducting tests, recording quality data
Work EnvironmentDesign and development labs, manufacturing plantsManufacturing floors, quality control labs
Employer & Industry UsageMedical device companies, OEMs, suppliersManufacturers, contract labs, quality departments

In summary, Quality Engineer Medical Devices focus on developing quality systems, process improvements, and ensuring compliance, while Quality Technicians primarily perform product inspections and testing. Both roles are essential in maintaining high standards in the medical device industry but differ in scope and responsibilities.

What are popular job titles related to Quality Engineer Medical Devices jobs in Virginia?

For Quality Engineer Medical Devices jobs in Virginia, the most frequently searched job titles are:

What job categories do people searching Quality Engineer Medical Devices jobs in Virginia look for?

The top searched job categories for Quality Engineer Medical Devices jobs in Virginia are:

What cities in Virginia are hiring for Quality Engineer Medical Devices jobs?

Cities in Virginia with the most Quality Engineer Medical Devices job openings:

Infographic showing various Quality Engineer Medical Devices job openings in Virginia as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 15% Part Time, and 5% Contract. Highlights an 92% Physical, 1% Hybrid, and 7% Remote job distribution, with an average salary of $83,318 per year, or $40.1 per hour.

Quality Engineer

Mpr Associates, Inc.

Alexandria, VA • On-site

$77K - $99K/yr

Full-time

Re-posted 16 days ago


Key responsibilities

  • Perform internal audits of the MPR quality program.

  • Perform supplier qualification activities, including on-site audits of suppliers.

  • Play a key role on the MPR Corrective Action Review Team by defining corrective actions, verifying their implementation, and assessing their effectiveness.


Job description

Overview

As the Quality Engineer at MPR, you play a key role in ensuring the MPR quality assurance program satisfies industry requirements and client expectations. This position provides strategic guidance to our project engineers to ensure the effective implementation of our quality program. In addition, you will work closely with the MPR leadership team to ensure appropriate corrective actions and continual improvement activities are implemented effectively.

Duties/Responsibilities

Typical duties and responsibilities for the role include an array of the following:

  • Perform internal audits of the MPR quality program.
  • Perform supplier qualification activities, including on-site audits of suppliers.
  • Play a key role on the MPR Corrective Action Review Team - define corrective actions and process improvement initiatives, verify their implementation, and assess their effectiveness.
  • Evaluate changes to industry standards to assess the impact on the MPR quality program.
  • Perform trend analyses of metrics used to measure quality program performance, supplier performance, and client satisfaction.
  • Perform general and project-specific oversight to ensure quality program requirements are implemented properly.
  • Review documentation to ensure contractual and quality program requirements are understood and satisfied.
  • Review hardware and software test procedures and results to ensure compliance with the MPR quality program.
  • Assemble the information needed to support management review meetings, prepare the resulting report, and follow-up on the actions assigned.
Qualifications

Education and Training

  • A bachelor's degree in a technical field, or equivalent technical experience, is required.
  • Professional certification(s) or training related to ASME NQA-1, ISO 13485, or ISO 9001 are desired.

Experience

  • Two or more years of experience in a technical organization performing engineering or manufacturing related activities is preferred.
  • Prior experience as a quality professional working under an ASME NQA-1, ISO 13485, or ISO 9001 based quality program with experience in performing audits and implementing corrective action and process improvement is preferred.
  • Prior experience with U.S. military quality assurance programs is a plus (such as the Navy Nuclear Quality Assurance program).
  • Proficiency with Microsoft Office applications, such as MS Outlook, Word, and Excel is required.

Leadership & Communication Skills

  • Persistent, questioning attitude and the ability to accept that in others.
  • Ability to multi-task across teams of engineers and managers on various projects.
  • Excellent verbal and written communication skills.
  • Ability to work collaboratively across functional teams.
  • Ability to accept and grow from constructive feedback.
  • Motivated to expand skills and knowledge, as well as tackle new problems and take on new responsibilities.
  • Ability to work in a dynamic and fast-paced environment.
  • Solution oriented with a goal of enabling our client's success.

 

Required

  • U.S. Citizenship is required.

 

Location: Alexandria VA (HQ)

 

Position Type: Full-time, Exempt

 

Travel: 10-20% as required by project assignments, including to support internal company audits or supplier audits, as well as to MPR branch offices. 

 

Work Environment: Collaborative with a heavy focus on quality processes and excellence behaviors-you'll support multiple concurrent projects across different technologies and regulatory frameworks, mentor staff and provide guidance to technical teams, and continuously expand your expertise in quality systems.

About MPR

Founded in 1964, MPR Associates provides independent engineering and consulting services to clients in the power and energy, federal, and life sciences sectors. The firm operates throughout the United States and internationally, making challenging projects successful by delivering safe and reliable technical solutions across the entire project lifecycle. Our independence from any single technology vendor or corporate parent allows us to provide objective technical advice and maintain broad expertise across the nuclear industry.

What truly sets MPR apart from our peers is:

The Work: Support quality assurance processes across projects in diverse regulated industries including nuclear reactor technologies (advanced fission, fusion, operating plants, research facilities) and medical devices. You'll serve as an internal QA resource ensuring our deliverables meet regulatory requirements and quality standards across varied projects and occasionally advise clients on QA implementation strategies. Supporting a broad client base means you'll enable our engineers' interactions with technology developers, manufacturers, regulators, and research institutions-while gaining exposure to multiple technologies and markets. You'll also have autonomy to identify and implement process improvements that strengthen MPR's quality systems and support our team's success.

 

The Culture Technical rigor and first-principles thinking define MPR's approach-not vendor procedures or corporate mandates. You'll work alongside bright, motivated engineers and project managers across mechanical, civil, electrical, chemical, and materials disciplines. Questioning attitudes and constructive feedback are valued here; technical accuracy matters more than hierarchy. It's a high-performance culture built on trust and respect since 1964.

 

Career Development Establish yourself as a recognized QA authority across regulated industries-nuclear and medical device-not just within one technology or compliance framework. You'll maintain professional breadth that keeps you relevant regardless of which technologies succeed commercially, while growing as a leader through mentorship of junior engineers, quality system management, internal and client engagement, and process development initiatives.

 

MPR Associates, Inc. is an equal opportunity and affirmative action employer, who participates in EVerify. All qualified applicants will receive consideration for employment without regard to race, color, national origin, sex, religion, age, disability, veteran's status, sexual orientation, gender identity, genetic information or any other classification as required by applicable laws. MPR is a certified Virginia Values Veterans (V3) employer.

 

Employment Type: FULL_TIME