At CMD Med Tech, 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 5-10 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: 5–10 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 ( 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

Also on the board Same function, level within a rung

Level

Manager

Location

Columbus, OH

Occupation

Bioengineers and Biomedical Engineers

Industry

Engineering Services

Posted

7 days ago

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