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Medical Device Development Jobs in Atlanta, GA (NOW HIRING)

As a Medical Device Engineer you will be working with cross-functional teams to drive and grow technical capabilities of the R&D organization. This is a hands-on medical device software engineer with ...

Orthopedic Medical Rep

Atlanta, GA ยท On-site

$82K - $113K/yr

We are a fully integrated company with internal resources dedicated to the development and promotion of medical supplies and device products. We believe that our proven products and customer focused ...

Embedded Engineer

Atlanta, GA ยท On-site

$53 - $54/hr

No Duration: 6 months with possible extension Client is a medical device company Strong experience in Embedded C/C++ development on microcontrollers (Bare-metal/RTOS). Expertise in hardware ...

Showing results 41-60

Medical Device Development information

See Atlanta, GA salary details

$27.9K

$51.4K

$77.9K

How much do medical device development jobs pay per year?

As of Sep 5, 2026, the average yearly pay for medical device development in Atlanta, GA is $51,370.00, according to ZipRecruiter salary data. Most workers in this role earn between $40,900.00 and $57,700.00 per year, depending on experience, location, and employer.

What is medical device development?

Medical device development is the process of designing, creating, testing, and bringing medical devices to market. This process involves multiple stages, including concept development, prototyping, preclinical and clinical testing, regulatory approval, and manufacturing. The goal is to ensure that new devices are safe, effective, and meet regulatory standards before they are used by healthcare professionals or patients. Teams in medical device development often include engineers, scientists, regulatory specialists, and quality assurance professionals.

What are the key skills and qualifications needed to thrive in medical device development, and why are they important?

To thrive in Medical Device Development, you need expertise in engineering or life sciences, a solid understanding of regulatory requirements, and often an advanced degree such as a master's or Ph.D. in a relevant field. Familiarity with CAD software, prototyping tools, and knowledge of FDA or ISO regulatory standards is typically required. Strong problem-solving abilities, collaboration, and effective communication distinguish top professionals in this field. These skills ensure the development of safe, innovative, and compliant medical devices that meet both user needs and regulatory standards.

What are some common challenges faced by professionals in medical device development, and how can they be addressed?

Professionals in medical device development frequently encounter challenges such as navigating complex regulatory requirements, ensuring product safety and efficacy, and managing cross-functional collaboration between engineering, clinical, and regulatory teams. Addressing these challenges requires staying updated on evolving regulations, fostering open communication among diverse team members, and implementing robust quality control processes. Proactively engaging with regulatory bodies and regularly reviewing project milestones can help streamline development and reduce the risk of costly delays.

What is the difference between Medical Device Development vs Medical Device Quality Assurance?

AspectMedical Device DevelopmentMedical Device Quality Assurance
CredentialsEngineering degrees, certifications like RAPS or regulatory trainingQuality certifications, ISO 13485, regulatory compliance training
Work EnvironmentDesign labs, R&D teams, product development settingsManufacturing sites, quality control labs, compliance departments
Industry UsageDesigning and creating new medical devicesEnsuring devices meet quality and regulatory standards

Medical Device Development focuses on designing and creating new medical devices, involving engineering and product innovation. Medical Device Quality Assurance ensures these devices meet safety, quality, and regulatory standards through testing and compliance processes. Both roles are essential in the medical device industry but serve different functions in the product lifecycle.

Infographic showing various Medical Device Development job openings in Atlanta, GA as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 15% Part Time, and 7% Contract. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $51,370 per year, or $24.7 per hour.

R&D Principal Engineer - Alpharetta, GA

Avanos Medical

Alpharetta, GA โ€ข On-site

Other

Medical, Life, Retirement

Re-posted 26 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