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Med Engineer Jobs (NOW HIRING)

Regulatory Quality Engineer

Kenosha, WI · On-site

$69K - $90K/yr

Complies with all applicable regulatory requirements for medical devices such as FDA Quality System ... Bachelor's degree in applicable technical discipline such as mechanical or bio-medical engineering ...

... Engineering, Bio-Medical Engineering, Interior Design, Architecture, Mechanical Engineering, Electrical Engineering, Plumbing Engineering, or equivalent required 12 years of experience minimum ...

Performing as a project leader in defining the requirements and specifications of medical ... Serves as a staff advisor to the Biomedical Engineering Supervisor/ Chief in Biomedical Engineering ...

... Engineering, Bio-Medical Engineering, Interior Design, Architecture, Mechanical Engineering, Electrical Engineering, Plumbing Engineering, or equivalent required 12 years of experience minimum ...

... Engineering, Bio-Medical Engineering, Interior Design, Architecture, Mechanical Engineering, Electrical Engineering, Plumbing Engineering, or equivalent required 12 years of experience minimum ...

... Engineering, Bio-Medical Engineering, Interior Design, Architecture, Mechanical Engineering, Electrical Engineering, Plumbing Engineering, or equivalent required 12 years of experience minimum ...

... Engineering, Bio-Medical Engineering, Interior Design, Architecture, Mechanical Engineering, Electrical Engineering, Plumbing Engineering, or equivalent required • 12 years of experience minimum ...

... Engineering, Bio-Medical Engineering, Interior Design, Architecture, Mechanical Engineering, Electrical Engineering, Plumbing Engineering, or equivalent required 12 years of experience minimum ...

... Engineering, Bio-Medical Engineering, Interior Design, Architecture, Mechanical Engineering, Electrical Engineering, Plumbing Engineering, or equivalent required 12 years of experience minimum ...

... Engineering, Bio-Medical Engineering, Interior Design, Architecture, Mechanical Engineering, Electrical Engineering, Plumbing Engineering, or equivalent required 12 years of experience minimum ...

Bio-Med Engineering Tech | 1.0 FT

Phelps, NY · On-site

$25.75 - $34.25/hr

The Bio-Med Engineering Technician works independently on repairs, safety testing and preventive maintenance of general clinical equipment. Maintains equipment records, writes reports, and ...

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Med Engineer information

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$39K

$101.8K

$137.5K

How much do med engineer jobs pay per year?

As of Sep 10, 2026, the average yearly pay for med engineer in the United States is $101,752.00, according to ZipRecruiter salary data. Most workers in this role earn between $84,000.00 and $116,500.00 per year, depending on experience, location, and employer.

What are popular job titles related to Med Engineer jobs?

For Med Engineer jobs, the most frequently searched job titles are:

Infographic showing various Med Engineer job openings in the United States as of August 2026, with employment types broken down into 94% Full Time, 2% Part Time, and 4% Contract. Highlights an 85% Physical, 5% Hybrid, and 10% Remote job distribution, with an average salary of $101,752 per year, or $48.9 per hour.

Regulatory Quality Engineer

Kenosha, WI • On-site

$69K - $90K/yr

Other

Posted 22 days ago


Job description

  • Acts as a Quality System Management Representative for the Elmhurst (IL) and Kenosha (WI) facilities.
  • Ensures the promotion of awareness of applicable regulatory requirements and quality management system requirements throughout the organization. Assists in training personnel on all aspects of the Quality System and regulatory standards.
  • Ensures that processes needed for the quality management system are established, implemented, and maintained.
  • Complies with all applicable regulatory requirements for medical devices such as FDA Quality System Regulation - 21 CFR 820, GMP guidelines, GDP, ISO 13485, ISO and other applicable regulatory requirements.
  • Leads and/or participates in the development, implementation, compliance, and maintenance of standards (FDA, ISO 13485:2016, etc.) and procedures.
  • Acts as a direct contact for FDA. Ensures FDA registrations and device listings are current.
  • Participates and supports the ECO, CAPA, MRB and other Quality System processes.
  • Creates metrics that drive effective monitoring of processes, value-add improvements and communication at all levels of the organization.
  • Develops and implements process flows in cooperation with functional groups.
  • Ensures risk assessment activities are executed and maintained according to regulatory standards.
  • Organizes investigation activities and coordinates appropriate resources to drive for root cause determinations, correction action implementation and effectiveness verification.
  • Leads vendor, internal/external, and process audits at both facilities and provides necessary documentation.
  • Performs validation training. Establishes and maintains master validation program, including site and individual products and process master validations.
  • Designs and oversees training program(s), including ISO internal training.
  • Responsible for internal and external audits.
  • Interferes with suppliers to resolve quality issues.
  • Coordinates manufacturing process validation requirements, documentation and maintenance of validated processes with internal and external stakeholders.
  • Other duties as assigned.

Qualifications

  • Bachelor's degree in applicable technical discipline such as mechanical or bio-medical engineering is strongly preferred or equivalent,
  • or five to ten years of experience in medical device manufacturing industry and in the quality engineering role, and/or training,
  • or equivalent combination of education and experience.
  • Knowledge of the medical device manufacturing industry.
  • Knowledge of ISO 13485 Quality Management System & FDA 21CFR 820 Regulations.
  • Knowledge of Geometric Dimensioning and Tolerancing per ASME Y14.5M.
  • Familiarity with test methods and standards for the design, verification, and validation of medical device products is required.
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Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws.For further information, please review the Know Your Rights notice from the Department of Labor.

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