Mid-Level Systems Engineer, MedTech – Hybrid (Columbus)

Hiring Steps Inc.; Columbus (OH); Hybrid; USD 110,000 - 150,000; Full time

Benefits offered by this job

401(k)

Bonus

Health

Life

PTO

Job summary

CMD MedTech in Columbus, OH is seeking a mid-level Systems Engineer with 7+ years in medical device regulatory and product development to lead and contribute to multi-disciplinary projects.

You will guide design reviews, write system requirements, risk management plans, and verification protocols, and collaborate with clients and teammates in a values-driven, collaborative culture. The role requires hybrid work with occasional travel.

Qualifications

• 7+ years in medical device regulatory and product development.
• Bachelor's degree in engineering.
• Strong leadership and communication skills.
• Able to work in a hybrid Columbus environment.

Responsibilities

• Lead and support medical device development and regulatory projects.
• Generate and review deliverables like requirements, risk assessments, 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.

Skills

Leadership

Written & verbal communication

Cross-functional collaboration

Regulatory knowledge

People management

Education

Bachelor's in Engineering

Job description

Based on experience Full Time Columbus, OH Hybrid 09/22/2026

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 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

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Screening Questions

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