Medical Device Systems Engineer

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

Benefits offered by this job

401(k)

Bonus

Health insurance

Life insurance

PTO

Job summary

CMD MedTech in Columbus, OH is hiring a mid-level Systems Engineer with 7+ years of medical device regulatory and product development experience. You will lead cross-functional efforts, help author system requirements, and drive risk management activities.

This hybrid role requires a strong communicator and hands-on leader who can manage design reviews, write risk assessments, and collaborate with clients. If you value teamwork and doing the right thing, CMD offers growth, stability, and a

Qualifications

• 7+ years of medical device regulatory and product development experience.
• Bachelor's degree in engineering (biomedical, mechanical, electrical, or similar).
• Strong leadership, collaboration, and communication skills.
• Able to balance detail work with high-level planning.
• Columbus-based with hybrid work and 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 align work with scope and schedule
• Build trust with clients and teammates through clear communication
• Contribute to CMD's collaborative, values-first culture

Skills

Medical device regulatory

Product development

Leadership

Clear communication

Collaborative teamwork

Education

Bachelor's in engineering (biomedical/mechanical/electrical)

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 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