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