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Medical Device Developer Jobs Near Me

IntelliGuard

Sr. Front End Developer

Columbus, OH · On-site

$111K - $145K/yr

As a Sr. Frontend Developer, you will be responsible for leading the development of complex ... Ensures compliance with medical device regulations, security standards, and industry best practices.

ICU Medical

Engineer III, Sustaining

Dublin, OH · On-site

$88K - $108K/yr

Knowledge of medical device packaging systems, packaging validation, and accelerated aging methodologies. * Experience managing engineering change processes within a regulated manufacturing ...

ICU Medical

Engineer III, Sustaining

Dublin, OH · On-site

$88K - $108K/yr

Knowledge of medical device packaging systems, packaging validation, and accelerated aging methodologies. * Experience managing engineering change processes within a regulated manufacturing ...

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How much do medical device developer jobs pay per year?

As of Aug 13, 2026, the average yearly pay for medical device developer in the United States is $97,383.00, according to ZipRecruiter salary data. Most workers in this role earn between $84,000.00 and $107,500.00 per year, depending on experience, location, and employer.

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Medical Device Developer jobs near you
A map of the United States highlighting the number of Medical Device Developer job openings by state according to ZipRecruiter. The image is accompanied by a detailed chart listing the number of Medical Device Developer job openings in each state, with California having the most at 2 and Alaska the least at 0.

Medical Device Systems Engineer

CMD MedTech

Columbus, OH • Hybrid

Full-time

Medical, Life, Retirement, PTO

Posted 20 days ago

Job description

At CMD MedTech, we believe strong relationships are just as important as strong technical skills. We’re a growing medical device engineering and regulatory consulting firm helping companies bring innovative, life-changing medical devices to market. Our team thrives on trust, flexibility, and follow-through.

We’re hiring a mid-level Systems Engineer with 7 or more years of relevant experience who’s a natural collaborator, a clear communicator, and a hands-on leader with a reputation for getting things done. You should be as comfortable leading a big design review as you are writing a safety risk management plan or authoring system requirements. Most of all, you should value openness, teamwork, and doing the right thing—even when it’s not the easiest path.

What You’ll Do

  • Lead and support medical device development and regulatory projects
  • Generate and review deliverables like requirements, risk assessments, regulatory strategies, or verification protocols
  • Facilitate team discussions and keep work aligned with scope and schedule
  • Build trust with clients and teammates through clear communication
  • Contribute to CMD’s collaborative, values-first culture

What You Bring

  • 7 or more years of medical device regulatory and product development experience
  • Bachelor’s in engineering (biomedical, mechanical, electrical, or similar)
  • Strong leadership, follow-through, and people skills
  • Comfort switching between detail work and high-level planning
  • Columbus-based and able to work hybrid with occasional travel (<25%)

Why CMD?

  • Real-world patient and caregiver impact
  • A team that values growth, integrity, and collaboration
  • Supportive environment to learn, take ownership, and stretch your skills
  • Competitive salary + 401(k) + bonus, health, life, PTO, and more