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Medical Device Engineer Jobs in Virginia (NOW HIRING)

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

Be Seen First

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 ...

Addison Group

Senior Staff Packaging Engineer

Leesburg, VA · On-site

$128K - $136K/yr

Lead the design, development, and implementation of sterile and non-sterile medical device packaging systems from concept through production release. * Develop packaging design standards, engineering ...

Addison Group

Senior Staff Packaging Engineer

Leesburg, VA · On-site

$128K - $136K/yr

Lead the design, development, and implementation of sterile and non-sterile medical device packaging systems from concept through production release. * Develop packaging design standards, engineering ...

BSI Prof Serv EHS West

Bachelor's or higher degree in a discipline relevant to the medical device industry. This may includeelectronic/electrical,electro-mechanical or biomedical engineering or medical physics.

BSI Group

Bachelor's or higher degree in a discipline relevant to the medical device industry. This may includeelectronic/electrical,electro-mechanical or biomedical engineering or medical physics.

Insight Global

Mechanical Engineer

Virginia Beach, VA · On-site

$36 - $46/hr

Insight Global's medical device manufacturer client is looking to bring a Mechanical Engineer onto their staff in Virginia Beach, VA. The Mechanical Engineer will be responsible for developing and ...

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 ...

IVWATCH LLC

Embedded Software Engineer

Newport News, VA · On-site

Position Summary ivWatch is seeking an Embedded Software Engineer to design, develop, test, and maintain embedded software for our medical device products. This role will work closely with software ...

ivWatch LLC

Embedded Software Engineer

Newport News, VA · On-site

$75K - $82K/yr

Position Summary ivWatch is seeking an Embedded Software Engineer to design, develop, test, and maintain embedded software for our medical device products. This role will work closely with software ...

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All JobsMedical Device Engineer JobsMedical Device Engineer Jobs in Virginia

Medical Device Engineer information

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How much do medical device engineer jobs pay per hour?

As of Aug 30, 2026, the average hourly pay for medical device engineer in Virginia is $49.41, according to ZipRecruiter salary data. Most workers in this role earn between $34.81 and $59.09 per hour, depending on experience, location, and employer.

What does a medical device engineer do?

A Medical Device Engineer is responsible for designing, developing, testing, and improving medical devices used in healthcare settings. They work closely with doctors, scientists, and regulatory bodies to ensure that devices are safe, effective, and compliant with industry standards. Their work includes creating prototypes, conducting risk assessments, and overseeing the manufacturing process. Medical Device Engineers play a crucial role in bringing innovative technologies to market that help diagnose, treat, or monitor medical conditions.

What does a medical device engineer do?

A medical device engineer is an engineering professional who develops new medical equipment and medical devices. As a medical device engineer, your work will vary depending on your area of expertise and may include biomedical research, material research and sourcing, computer-aided design work, and teaming up with doctors and patients. You also must understand the manufacturing process and ensure the products you design are both useful and cost-effective. You look for innovative solutions to medical problems and design new equipment diagnoses and treatments.

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

To thrive as a Medical Device Engineer, you need a solid background in biomedical, mechanical, or electrical engineering, often supported by a relevant bachelor's or master's degree. Familiarity with CAD software, regulatory standards (such as FDA or ISO 13485), and design validation tools is typically required. Strong problem-solving, communication, and teamwork skills are essential for collaborating on multidisciplinary projects and ensuring product safety. These competencies are crucial for developing innovative, compliant devices that improve patient outcomes and meet rigorous industry standards.

What are some common challenges medical device engineers face when bringing a new product from concept to market?

Medical Device Engineers often encounter challenges such as navigating complex regulatory requirements, ensuring product safety and efficacy, and coordinating with cross-functional teams including design, manufacturing, and quality assurance. Balancing innovation with compliance, managing timelines, and addressing unforeseen technical issues are also typical hurdles. Successful engineers leverage strong project management and communication skills to collaborate effectively and bring devices to market efficiently.

What is the difference between Medical Device Engineer vs Biomedical Engineer?

AspectMedical Device EngineerBiomedical Engineer
CredentialsBachelor's or Master's in Engineering, certifications in medical device designBachelor's or Master's in Biomedical Engineering or related field
Work EnvironmentDesign, develop, test medical devices in labs or manufacturing settingsResearch, develop medical equipment, or work in clinical settings
Industry UsagePrimarily in medical device manufacturing companiesHospitals, research institutions, medical device companies

Medical Device Engineers focus on designing and testing specific medical devices, ensuring compliance and safety. Biomedical Engineers have a broader scope, working on medical equipment, implants, and research. Both roles require similar credentials and often overlap in industry settings, but their primary focus differs.

More about Medical Device Engineer jobs

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

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

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

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

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

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

What cities in Virginia are hiring for Medical Device Engineer jobs?

Cities in Virginia with the most Medical Device Engineer job openings:

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

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

Medical Device Engineer jobs near you
Infographic showing various Medical Device Engineer job openings in Virginia as of August 2026, with employment types broken down into 91% Full Time, 2% Part Time, 2% Temporary, and 5% Contract. Highlights an 95% In-person, 3% Hybrid, and 2% Remote job distribution, with an average salary of $102,773 per year, or $49.4 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

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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.