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Quality Engineer Medical Device Jobs in Virginia

Caraballo Consulting & Associates L

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QA Manufacturing Engineer - Medical Device

Sterling, VA · On-site

$40 - $80/hr

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 ...

Caraballo Consulting & Associates L

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QA Manufacturing Engineer - Medical Device

Sterling, VA · On-site

$40 - $80/hr

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 ...

Pop-Up Talent

Principal QAE

Charlottesville, VA · On-site

$112K - $136K/yr

At least 8+ years of Quality Assurance/Quality Engineering experience in medical device manufacturing * Experience with mechanical and electrical products * ASQ Certified Quality Engineer (CQE) or ...

Euclid Vision Corporation

Senior Quality Engineer

Sterling, VA · On-site

$89K - $121K/yr

Euclid Vision Corporation is a growing medical device organization specializing in orthokeratology ... As we scale across our group of companies, we're looking for a Senior Quality Engineer who wants ...

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Senior Quality Engineer

Sterling, VA · On-site

$105 - $130/hr

Euclid Vision Corporation is a growing medical device organization specializing in orthokeratology ... As we scale across our group of companies, we're looking for a Senior Quality Engineer who wants ...

New

Aurora Lifesciences

Senior Quality Engineer

Manassas, VA · On-site

$95 - $125/hr

Experience within medical device manufacturing or another ISO 13485 regulated environment would be particularly valuable. The Person This role will suit a Senior Quality Engineer who enjoys taking ...

New

Instant Systems Inc

Quality Engineer

Norfolk, VA

$69K - $90K/yr

... including medical device components. The ideal candidate will have hands-on experience in a ... Mechanical engineering experience preferred Knowledge of Quality Engineering and Advanced Quality ...

Instant Systems Inc

Quality Engineer

Norfolk, VA

$62K - $80K/yr

... including medical device components. The ideal candidate will have hands-on experience in a ... Knowledge of Quality Engineering and Advanced Quality principles (Six Sigma methodology, Root Cause ...

LifeNet Health

Quality Engineer I

Virginia Beach, VA

$64K - $83K/yr

... the medical device/biologics/tissue combination product industry. This role involves cross-functional initiatives and serving as the Quality Engineering representative in design and production ...

LifeNet Health

Quality Engineer I

Virginia Beach, VA · On-site

$75.84 - $101.12/hr

... the medical device/biologics/tissue combination product industry. This role involves cross-functional initiatives and serving as the Quality Engineering representative in design and production ...

LifeNet Health

Quality Engineer I

Virginia Beach, VA · On-site

$68K - $88K/yr

... the medical device/biologics/tissue combination product industry. This role involves cross-functional initiatives and serving as the Quality Engineering representative in design and production ...

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All JobsQuality Engineer Medical Device JobsQuality Engineer Medical Device Jobs in Virginia

Quality Engineer Medical Device information

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How much do quality engineer medical device jobs pay per hour?

As of Aug 29, 2026, the average hourly pay for quality engineer medical device in Virginia is $36.41, according to ZipRecruiter salary data. Most workers in this role earn between $24.57 and $45.53 per hour, 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 medical devices meet all regulatory standards and quality requirements. They develop and implement quality assurance processes, perform risk assessments, and conduct inspections and audits to make sure products are safe and effective. Quality Engineers also collaborate with design, manufacturing, and regulatory teams to resolve quality issues and improve product reliability. Their work is crucial for maintaining compliance with standards such as ISO 13485 and FDA regulations.

What are the key skills and qualifications needed to thrive as a quality engineer in the medical device industry?

To thrive as a Quality Engineer in the medical device industry, you need a strong background in quality assurance, regulatory compliance (such as ISO 13485 and FDA 21 CFR Part 820), and engineering principles, often supported by a relevant engineering degree. Familiarity with quality management systems (QMS), risk analysis tools (like FMEA), and certifications such as CQE (Certified Quality Engineer) are typically required. Attention to detail, problem-solving, and effective communication are critical soft skills for collaborating with cross-functional teams and ensuring product safety. These skills and qualifications are vital to maintain regulatory compliance, uphold product quality, and protect patient safety in a highly regulated environment.

How does a quality engineer in the medical device industry typically collaborate with cross-functional teams to ensure product compliance?

Quality Engineers in the medical device sector work closely with cross-functional teams such as design, manufacturing, regulatory affairs, and supply chain. They participate in design reviews, risk assessments, and process validations to ensure that products meet both internal quality standards and external regulatory requirements (such as FDA or ISO 13485). Regular collaboration involves reviewing documentation, addressing non-conformances, and implementing corrective actions. This teamwork is critical to proactively identify potential issues and maintain continuous product quality throughout the development and production lifecycle.

What is the difference between Quality Engineer Medical Device vs Quality Assurance Specialist Medical Device?

AspectQuality Engineer Medical DeviceQuality Assurance Specialist Medical Device
CertificationsISO 13485, Six Sigma, ASQ certificationsISO 13485, Six Sigma, ASQ certifications
Work EnvironmentDesign, development, manufacturing, and process improvementAuditing, compliance, documentation, and process verification
Employer & Industry UsageMedical device manufacturers, R&D labsMedical device companies, regulatory agencies, consulting firms

While both roles focus on quality in the medical device industry, a Quality Engineer Medical Device primarily works on product design, process development, and continuous improvement. In contrast, a Quality Assurance Specialist Medical Device emphasizes compliance, auditing, and ensuring adherence to regulatory standards. Both roles are essential for maintaining product safety and quality, but they differ in scope and daily responsibilities.

More about Quality Engineer Medical Device jobs

What are the most commonly searched types of Quality Engineer Medical Device jobs in Virginia?

The most popular types of Quality Engineer Medical Device jobs in Virginia are:

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

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

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

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

Quality Engineer Medical Device jobs near you
Infographic showing various Quality Engineer Medical Device job openings in Virginia as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 88% Physical, 1% Hybrid, and 11% Remote job distribution, with an average salary of $75,729 per year, or $36.4 per hour.

QA Manufacturing Engineer - Medical Device

Sterling, VA • On-site

Caraballo Consulting & Associates L
See more jobs at Caraballo Consulting & Associates Lexternal

$40 - $80/hr

Contractor

Posted 11 days ago

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Job description

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 candidate will perform the following activities:

Key Responsibilities:

    • Support quality assurance activities associated with transferring and starting up manufacturing operations at the new site.
    • Review, execute, and approve validation documentation, including protocols, test scripts, test data, and final reports.
    • Provide QA oversight for process validation activities to ensure processes are qualified, controlled, and appropriately documented.
    • Support equipment qualification efforts, including IQ, OQ, and PQ activities for manufacturing equipment and related systems.
    • Partner with Manufacturing, Engineering, Validation, and Quality teams to ensure validation deliverables are completed on time and in compliance with applicable procedures and regulations.
    • Assess validation packages for completeness, accuracy, traceability, and adherence to GMP and medical device quality system requirements.
    • Support investigation and resolution of validation-related deviations, discrepancies, and change controls.
    • Generate, review, and approve validation summary reports and supporting documentation for management and quality records.                  
    • Support QA activities associated with the QMS integration of 2 companies.
    • Modify SOPs to complete QMS integration.
    • Complete Change Control activities.
    • Complete the bulk download of documents and records from a Quality Management System.

   Required Qualifications:

  • Bachelor’s degree in Engineering, Quality, Life Sciences, or a related technical discipline, or equivalent relevant experience.
  • Experience in the medical device industry within Quality Assurance, Validation, Manufacturing Quality, or a closely related function.
  • Strong working knowledge of process validation, equipment qualification, and GMP requirements in a regulated manufacturing environment.
  • Demonstrated experience reviewing and approving validation documentation and technical reports.
  • Familiarity with manufacturing operations and the practical application of quality requirements on the production floor.
  • Ability to work independently while coordinating effectively with cross-functional stakeholders.
  • Strong technical writing, documentation review, and problem-solving skills.
  • Excellent attention to detail and ability to manage multiple priorities within a time-bound project.

Company Description

We are a specialized Global staffing firm that works for Fortune 500 companies in the Medical Device, Pharmaceutical, and Biotec industries, finding qualified personnel.