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Cleaning Validation Engineer Medical Devices Jobs

The Validation Engineer II supports a broad range of software-enabled medical devices within a product suite that includes intraoperative neuromonitoring, surgical alignment, robotic navigation, and ...

... or cleaning validation. The individual will coordinate validation activities with the client and ... devices is strongly desired. * Experience using statistical tools is a plus to analyze data ...

... or cleaning validation. The individual will coordinate validation activities with the client and ... devices is strongly desired. * Experience using statistical tools is a plus to analyze data ...

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Cleaning Validation Engineer Medical Devices information

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How much do cleaning validation engineer medical devices jobs pay per hour?

As of Sep 14, 2026, the average hourly pay for cleaning validation engineer medical devices in the United States is $52.00, according to ZipRecruiter salary data. Most workers in this role earn between $39.42 and $63.22 per hour, depending on experience, location, and employer.

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Infographic showing various Cleaning Validation Engineer Medical Devices job openings in the United States as of September 2026, with employment types broken down into 56% Full Time, 3% Temporary, and 41% Contract. Highlights an 100% In-person job distribution, with an average salary of $108,152 per year, or $52 per hour.

Senior Hardware Engineer Medical Devices

Tarrytown, NY โ€ข On-site

Tekfortune Inc.
Recruiting and Staffing Servicesย โ€ขย 11 - 50 employees

$117K - $156K/yr

Other

Posted 3 days ago

New


Job description

Senior Hardware Engineer โ€“ Medical Devices

Location: Tarrytown, NY

Must-Have Skills

  • 10+ years of experience in Medical Device Hardware Development
  • Analog, Digital & Mixed-Signal Design
  • MCU, FPGA, Sensor Interface Design
  • Power Electronics, Battery-Powered Devices, DC-DC Converters
  • High-Speed PCB Design (Ethernet, USB, SPI, I2C, CAN)
  • PCB Design, DFM, DFT, SI/PI Analysis
  • CAPA, NCR, Change Control & Obsolescence Management
  • Component Qualification & Alternate Part Evaluation
  • Hardware Verification & Validation (V&V)
  • Risk Management (dFMEA, pFMEA, sFMEA)
  • Requirement Traceability (RTM)
  • IEC 60601-1, IEC 60601-1-2, ISO 14971, ISO 13485
  • FDA Medical Device Regulations
  • Manufacturing Transfer & Sustaining Engineering
  • Windchill / Agile PLM

Preferred Skills

  • IVD / Clinical Diagnostics / Medical Equipment
  • Cost Reduction, VAVE & Should-Cost Analysis
  • Safety & EMC Compliance Testing
  • Supplier Qualification & Product Lifecycle Management
  • Agile / Scrum Project Execution

Key Responsibilities

  • Lead hardware design, development, and sustaining engineering activities for regulated medical devices.
  • Drive CAPA, change management, obsolescence mitigation, and product improvement initiatives.
  • Perform schematic reviews, component selection, PCB design reviews, and hardware validation.
  • Execute risk assessments, V&V, compliance testing, and regulatory support activities.
  • Support manufacturing transfers, supplier changes, and cost optimization programs.
  • Collaborate with Systems, Firmware, Mechanical, Quality, Regulatory, and Manufacturing teams.

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About Tekfortune

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Industry

Recruiting and staffing services

Company size

11 - 50 Employees

Headquarters location

Piscataway, NJ, US

Year founded

2014