SYSTEMS ENGINEER

Grove Gallery & Interiors; Columbus (OH); On-site; USD 90,000 - 120,000; Full time

Benefits offered by this job

Competitive salary

401(k) with company match

Health insurance

Paid time off

Bonus

Job summary

CMD MedTech is a growing medical device engineering and regulatory consulting firm in Columbus, OH. We seek a mid-level Systems Engineer with 5–10 years’ experience who leads with collaboration and clear communication, balancing hands-on work with design reviews and system requirements.

You’ll contribute to regulatory strategies, risk management, and verification protocols while supporting client projects and fostering an openness, teamwork, and integrity driven culture.

Qualifications

• 5–10 years of medical device regulatory and product development experience.
• Bachelor’s in engineering (biomedical, mechanical, electrical, or similar).
• Strong leadership and teamwork skills; effective communicator.
• Hybrid work model in Columbus with occasional travel (<25%).

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 ensure alignment with scope and schedule.
• Build trust with clients and teammates through clear communication.
• Contribute to CMD’s collaborative, values-first culture.

Skills

Leadership

Communication

Collaboration

Problem-solving

Regulatory knowledge

Education

Bachelor’s in engineering (biomedical, mechanical, electrical, or similar)

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 Engineerwith 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 (<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