Medical Device Systems Engineer

About the role

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.

Responsibilities

• 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

Requirements

• 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

Benefits

• Competitive salary
• 401(k) + bonus
• Health and life insurance
• Paid time off (PTO)

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