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Quality Engineer Medical Devices Jobs in Ohio (NOW HIRING)

IBA Worldwide

$74.18 - $97.01/hr

Embedded Firmware Engineer (Medical Devices) (m/f/d) - Nürnberg Requisition ID: 4480 Location: Schwarzenbruck, DE Work regime: Full-Time Kind of contract: Open Ended Contract Mission At IBA ...

Rust Belt Recruiting

Quality Engineer

Brook Park, OH · On-site

$80K - $90K/yr

... medical devices. Operating out of a modern, clean, 100% climate-controlled facility, our team maintains a collaborative, non-union environment focused on excellence. We are seeking a Quality Engineer ...

Belcan

Electrical Engineer

Cincinnati, OH · On-site

$50 - $60/hr

Electrical Engineer - Medical Devices Pay Rate: $50-60/hr Duration: 24-month contract Location ... Experience collaborating with mechanical, firmware, systems, quality, regulatory, manufacturing ...

Abbott

$62K - $80K/yr

Quality Engineer I Location: Atlanta, GA Duration: 12 Months 100% Onsite Position Summary The ... medical devices, nutritional and branded generic medicines. Working together, Abbott and Talent ...

Midmark

R+D Quality Engineer III

Versailles, OH · On-site

$66K - $86K/yr

JOB SUMMARY: The R + D Quality Engineer III leads and enforces product development quality ... of medical devices. ESSENTIAL/PRIMARY DUTIES: * Plans, leads, and manages quality deliverables on ...

Midmark Corporation

R+D Quality Engineer III

Versailles, OH · On-site

$66K - $86K/yr

JOB SUMMARY: The R + D Quality Engineer III leads and enforces product development quality ... of medical devices. ESSENTIAL/PRIMARY DUTIES: * Plans, leads, and manages quality deliverables on ...

NAM Info Inc

Senior Medical Device Engineer

Blue Ash, OH · On-site

$96K - $131K/yr

Manage cross-functional teams across Engineering, Quality, Regulatory, Manufacturing, Supply Chain ... Required Qualifications * 7+ years of experience in Medical Devices or other regulated industries.

New

Midmark

Quality Engineer II

Versailles, OH · On-site

$66K - $86K/yr

... of medical devices and components. Cross-functionally collaborates with R+D engineering ... Drives product quality improvements internally and externally by working with design, manufacturing ...

Midmark Corporation

Quality Engineer II

Versailles, OH · On-site

$66K - $86K/yr

... of medical devices and components. Cross-functionally collaborates with R+D engineering ... Drives product quality improvements internally and externally by working with design, manufacturing ...

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Showing results 1-20

All JobsQuality Engineer Medical Devices JobsQuality Engineer Medical Devices Jobs in Ohio

Quality Engineer Medical Devices information

See Ohio salary details

$42.8K

$79.9K

$113.1K

How much do quality engineer medical devices jobs pay per year?

As of Sep 5, 2026, the average yearly pay for quality engineer medical devices in Ohio is $79,896.00, according to ZipRecruiter salary data. Most workers in this role earn between $68,400.00 and $88,400.00 per year, depending on experience, location, and employer.

What does a quality engineer do in the medical device industry?

A Quality Engineer in the medical device industry is responsible for ensuring that products meet regulatory standards and quality requirements throughout their lifecycle. They develop and implement quality control processes, conduct risk assessments, lead investigations into product defects, and work closely with cross-functional teams to ensure compliance with regulations such as FDA and ISO 13485. Their work helps to guarantee the safety, reliability, and effectiveness of medical devices before they reach patients.

How does a quality engineer collaborate with cross-functional teams in the medical device industry?

Quality Engineers in the medical device field work closely with design, manufacturing, and regulatory teams to ensure products meet stringent quality and compliance standards. They participate in design reviews, help develop verification and validation protocols, and support the implementation of corrective actions. Regular communication with production and R&D teams is essential to identify potential risks early and to ensure that quality is built into every stage of product development. This collaborative approach not only improves product safety and efficacy but also streamlines regulatory submissions and audits.

What are the key skills and qualifications needed to thrive as a quality engineer in medical devices, and why are they important?

To thrive as a Quality Engineer in Medical Devices, you typically need a degree in engineering or a related field, combined with knowledge of quality assurance principles and regulatory requirements (such as ISO 13485 and FDA regulations). Familiarity with risk management tools, validation protocols, and quality management systems (QMS), as well as certifications like CQE (Certified Quality Engineer), are highly valuable. Strong analytical thinking, attention to detail, and effective communication skills enable you to identify issues, collaborate with cross-functional teams, and ensure compliance. These competencies are crucial for maintaining product safety, meeting regulatory standards, and supporting a culture of continuous improvement in the medical device industry.

What is the difference between Quality Engineer Medical Devices vs Quality Technician Medical Devices?

AspectQuality Engineer Medical DevicesQuality Technician Medical Devices
CertificationsISO 13485, Six Sigma, ASQ certificationsISO 13485, basic quality certifications
ResponsibilitiesDesigning quality systems, process improvements, root cause analysisInspecting products, conducting tests, recording quality data
Work EnvironmentDesign and development labs, manufacturing plantsManufacturing floors, quality control labs
Employer & Industry UsageMedical device companies, OEMs, suppliersManufacturers, contract labs, quality departments

In summary, Quality Engineer Medical Devices focus on developing quality systems, process improvements, and ensuring compliance, while Quality Technicians primarily perform product inspections and testing. Both roles are essential in maintaining high standards in the medical device industry but differ in scope and responsibilities.

What are popular job titles related to Quality Engineer Medical Devices jobs in Ohio?

For Quality Engineer Medical Devices jobs in Ohio, the most frequently searched job titles are:

What job categories do people searching Quality Engineer Medical Devices jobs in Ohio look for?

The top searched job categories for Quality Engineer Medical Devices jobs in Ohio are:

Quality Engineer Medical Devices jobs near you
Infographic showing various Quality Engineer Medical Devices job openings in Ohio as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 14% Part Time, 1% Temporary, and 7% Contract. Highlights an 92% Physical, 1% Hybrid, and 7% Remote job distribution, with an average salary of $79,896 per year, or $38.4 per hour.

Senior Electrical Sustenance Engineer-Medical Devices

3B Staffing LLC

Cincinnati, OH

$103K - $134K/yr

Full-time

Posted 13 days ago

Job description

Hello

Greetings!!!

This is Sakshi from Jconnect INC. Below is the requirement with my client. Please let me know if you are available for this role.

Title: Senior Electrical Sustenance Engineer-Medical Devices

Location : Blue Ash, OH

Duration: Fulltime

JOB DESCRIPTION:

Technical Skills

  • Analog & Digital Circuit Design - Strong design and troubleshooting skills.
  • Schematics and PCB Design Layout - Proficient in tools like Altium, OrCAD; knowledge of DFM/DFT.
  • Component Engineering - Obsolescence management, alternate sourcing.
  • Medical Standards Compliance - IEC 60601, ISO 13485, FDA 21 CFR Part 820.
  • Failure Analysis - Root cause analysis (FMEA, 5 Whys, Fishbone).
  • Verification & Validation - Test planning, execution, and documentation.
  • Embedded Systems (Preferred) - Basic understanding of firmware/hardware integration.
  • Documentation & PLM Tools - BOMs, ECOs, DHF; tools like Agile, Windchill.

Functional Skills

  • Sustaining Engineering - Support for legacy products and design updates.
  • Cross-Functional Collaboration - Work with QA, RA, Manufacturing, and Supply Chain.
  • Regulatory Knowledge - Understanding of global compliance requirements.
  • Project Management - Multitasking, prioritization, and milestone tracking.
  • Continuous Improvement - Lean/Six Sigma knowledge preferred.

If you are interested, please send me your updated resume ASAP with below details:

Full Name:

Current Location/Zip:

Contact Number:

E-Mail Id:

Alternate Email Id:

Visa/Work Permit Status:

Current Rate/Salary:

Expected Base Salary:

Notice Period/Availability to Start:

Skype ID:

Willingness to relocate to job location:

Any Relocation Concern (family/house/weather):

Current/Previous Employer Name:

Preferred Interview timings (Specify Time zone):

Any other job opportunity in process & at which stage:

Overall Experience Summary:

LinkedIn URL:

Looking forward for your response..

Thanks and Regards,

Sakshi Tripathi

Jconnect Infotech Inc.

168 Barclay Center Ste. 347,

Cherry Hill, NJ 08034

Contact : 856-569-1812

Email: sakshi@jconnectinc.com

LinkedIn ID: https://www.linkedin.com/in/sakshitripathi292000/

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