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Medical Device Validation Engineer Jobs in Georgia

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.

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.

Embedded Firmware Engineer

Ball Ground, GA ยท On-site

$96K - $131K/yr

The Firmware Engineer will be responsible for providing cross-functional engineering project ... Familiarity with the Medical Device Directive/Regulation (MDD/MDR), ISO 13485, FDA design controls ...

Embedded Firmware Engineer

Ball Ground, GA ยท On-site

$96K - $131K/yr

The Firmware Engineer will be responsible for providing cross-functional engineering project ... the Medical Device Directive/Regulation (MDD/MDR), ISO 13485, FDA design controls or similar ...

Quality Engineer Location: Kennesaw, Ga Schedule: Monday - Friday, 8am- 5pm TRC Talent Solutions is ... medical device industry. * Experience with process validation, risk management, statistical ...

Bachelor's degree or equivalent educational background in Analytical Sciences, Engineering ... Health: Medical, dental and vision insurance, life insurance, employee assistance programs.

Showing results 41-60

Medical Device Validation Engineer information

What are some common challenges faced by medical device validation engineers during the validation process?

Medical Device Validation Engineers often encounter challenges such as ensuring compliance with evolving regulatory standards, managing tight project timelines, and coordinating cross-functional teams. Additionally, they must address unexpected technical issues that arise during testing and validation, and meticulously document results to meet quality and audit requirements. Effective communication and adaptability are crucial for successfully navigating these challenges and delivering safe, effective medical devices.

What does a medical device validation engineer do?

A Medical Device Validation Engineer is responsible for ensuring that medical devices meet regulatory and quality standards before they reach the market. They design and execute tests to validate that products perform as intended, documenting procedures and results to comply with industry regulations such as FDA and ISO guidelines. Their work involves collaborating with design, manufacturing, and quality assurance teams to identify risks and verify that devices are safe and effective for use. This role is crucial for patient safety and for a company's ability to market medical products globally.

Are medical device validation engineers in demand?

Medical device validation engineers are in high demand due to the increasing regulation and complexity of medical devices. They play a critical role in ensuring compliance with standards like ISO 13485 and FDA requirements, and their expertise in validation, testing, and quality assurance is sought after in the healthcare industry.

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

AspectMedical Device Validation EngineerQuality Assurance Engineer
CredentialsEngineering degree, certifications like CQE or validation-specific trainingEngineering or related degree, CQE or QA certifications
Work EnvironmentDesign validation, process validation, testing labsAudits, process improvements, compliance documentation
Industry UsageProduct development, validation phases in medical device manufacturingEnsuring overall product quality, compliance, and process control

The Medical Device Validation Engineer focuses on validating medical devices through testing and process validation, ensuring products meet regulatory standards. In contrast, the Quality Assurance Engineer oversees overall quality systems, audits, and compliance processes. Both roles require similar certifications and work within the medical device industry, but their core responsibilities differ in scope and focus.

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

To thrive as a Medical Device Validation Engineer, you need a strong background in biomedical engineering or a related field, with expertise in validation protocols, regulatory compliance, and risk analysis. Familiarity with technical standards such as ISO 13485, FDA 21 CFR Part 820, and tools like statistical analysis software and validation management systems is essential. Attention to detail, problem-solving abilities, and effective communication are critical soft skills for collaborating with cross-functional teams and ensuring product safety. These skills are crucial to guarantee that medical devices meet regulatory requirements, function safely, and reach the market efficiently.
What are popular job titles related to Medical Device Validation Engineer jobs in Georgia? For Medical Device Validation Engineer jobs in Georgia, the most frequently searched job titles are:
What cities in Georgia are hiring for Medical Device Validation Engineer jobs? Cities in Georgia with the most Medical Device Validation Engineer job openings:
    Infographic showing various Medical Device Validation Engineer job openings in Georgia as of August 2026, with employment types broken down into 66% Full Time, 6% Temporary, and 28% Contract. Highlights an 95% In-person, and 5% Remote job distribution.

    R&D Principal Engineer - Alpharetta, GA

    Avanos Medical

    Alpharetta, GA โ€ข On-site

    Other

    Medical, Life, Retirement

    Re-posted 2 days ago


    Job description

    Requisition ID: 7089

     

    Job Title: R&D Principal Engineer - Alpharetta, GA

     

    Job Country: United States (US)

    Here at Avanos Medical, we passionately believe in three things:

    • Making a difference in our products, services and offers, never ceasing to fight for groundbreaking solutions in everything we do;
    • Making a difference in how we work and collaborate, constantly nurturing our nimble culture of innovation;
    • Having an impact on the healthcare challenges we all face, and the lives of people and communities around the world.

    At Avanos you will find an environment that strives to be independent and different, one that supports and inspires you to excel and to help change what medical devices can deliver, now and in the future. 

    Avanos is a medical device company focused on delivering clinically superior breakthrough solutions that will help patients get back to the things that matter. We are committed to creating the next generation of innovative healthcare solutions which will address our most important healthcare needs, such as reducing the use of opioids while helping patients move from surgery to recovery. Headquartered in Alpharetta, Georgia, we develop, manufacture and market recognized brands in more than 90 countries. For more information, visit www.avanos.com.

    The Role

    The Principal Engineer will support the Front End Innovation department assessing high level technical assessment and feasibility of products to innovate medical devices that advance patient care. This position combines hands-on design ownership, strong technical problem-solving, and cross-functional collaboration to ensure products meet user needs, regulatory requirements, and business objectives. The Principal Engineer is responsible for leading design workstreams within complex programs, mentoring junior engineers, and ensuring engineering excellence throughout the product development lifecycle.

    They will be consultants for the rest of the organization sharing their skillset and expertise in material science. Requires a professional with experience in Research and Development or New Product Development to deliver on the product development roadmap growing Avanosโ€™ enteral feeding business particularly in the development of our silicone balloon line.

    This candidate must act as a senior technical leader within the company and recognized internally for technical expertise in the field of material science silicones and elastomers, innovation, and test method excellence. The Principal Engineer will provide hands-on technical leadership to projects and moderate teams (2โ€“5 people), driving innovation, execution, and problem-solving on incremental to breakthrough initiatives.

    Key Responsibilities

    • Lead design and development activities for assigned subsystems or product components through the early phases of PDP.

    • Partner with third parties to help monitor and test the performance of current materials. Research new/better materials that can be used for existing products. Spec out and/or design materials to support the development of new products.

    • Collaborate with cross-functional partners (Marketing, Industrial Design, Clinical, Regulatory, Project Head) to complete high level technical assessment and burn down high-risk technical issues.

    • Support early front-end research conducting ethnography and listening to voice of customer to uncover unmet needs, high level technical assessment of materials and process, feasibility testing and test method development, and creating prototypes.

    • Apply sound engineering principles in areas such as mechanical design, fluidics, materials, and electromechanical integration to develop effective solutions.

    • Work with marketing teams to ensure designs address customersโ€™ needs.

    • Mentor and provide technical guidance to junior engineers within the team.

    • Support intellectual property development through design innovation and technical documentation.

    Your Qualifications

    Required

    • B.S. degree in polymer science/engineering, chemistry, chemical engineering, materials science, or any other related field, with 12+ years of experience,

    • Or Master of Science in polymer science/engineering, chemistry, chemical engineering, materials science, or any other related field, with 10+ years of experience,

    • Or PhD in polymer science/engineering, chemistry, chemical engineering, materials science, or any other related field, with 8+ years of experience with a focus on silicone or elastomers

    • Experience with electromechanical systems, fluid delivery, or disposable/reusable medical device interfaces.

    • Experience with silicone elastomers, thermoplastics, balloon dipping, or medical device polymer characterization.

    • Demonstrated experience leading design efforts for Class II or III medical devices.

    • Proven ability to solve complex technical problems and drive projects to completion in a matrixed environment.

    • Excellent written and verbal communication skills, with attention to design documentation and traceability.

    Preferred                                                                                                                  

    • Experience in statistical data analysis and design of experiments.

    • Strong proficiency in 3D CAD (SolidWorks preferred), GD&T, and mechanical design fundamentals.

    • Working knowledge of materials selection, molding processes, or sterilization methods (EO, gamma, e-beam).

    • Experience collaborating with contract manufacturers or development partners.

    • Participation in IP generation or patent applications

    The statements above are intended to describe the general nature and level of work performed by employees assigned to this classification. Statements are not intended to be construed as an exhaustive list of all duties, responsibilities and skills required for this position.

    Salary Range:

    The anticipated average base pay range for this position is $112,212 โ€“ 149,242. In addition, this role is eligible for an attractive incentive compensation program and benefits. In specific locations, the pay range may vary from the base posted.

    Avanos Medical is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, sexual orientation, gender identity or any other characteristic protected by law.

    IMPORTANT: If you are a current employee of Avanos or a current Avanos Contractor, please apply here.

    Join us at Avanos
    Join us and you can make a difference in our products, solutions and our culture. Most of all, you can make a difference in the lives, people, and communities around the world.

    Make your career count
    Our commitment to improving the health and wellbeing of others begins with our employees โ€“ through a comprehensive and competitive range of benefits. We provide more than just a salary โ€“ our Total Rewards package encompasses everything you receive as an employee; your pay, health care benefits, retirement plans and work/life benefits.

    Avanos offers a generous 401(k) employer match of 100% of each pretax dollar you contribute on the first 4% and 50% of the next 2% of pay contributed with immediate vesting.

     

    Avanos also offers the following:

    benefits on day 1

    free onsite gym

    onsite cafeteria

    HQ region voted 'best place to live' by USA Today

    uncapped sales commissions