V&v Intern

GE Healthcare · Healthcare · Haifa, Haifa District, Israel · Engineering / Technology

Responsible for planning and implementing verification methodologies for PET medical products, ensuring system and sub-system requirements are met. This involves reviewing designs, verifying functionality, determining testing environments, analyzing failures, and collaborating with development teams. The role requires a strong background in multi-disciplinary medical product testing and software QA processes.

What you'd actually do

  1. Responsible for planning and implementing verification methodologies and ensuring proper fulfillment of system and sub-system requirements.
  2. Responsible for reviewing various product designs, verifying its functionality in agile testing methods.
  3. Responsible to determine the testing environments and tools.
  4. Analyze and debug system failures and issue found during testing, while delivering detailed reports identifying these issues for further investigation.
  5. Work closely with development teams

Skills

Required

  • B.Sc. in Mechanical / Bio-Medical / Electronic Engineering
  • 3+ years of experience in multi-disciplinary medical products manual/automation testing
  • strong knowledge of software QA processes
  • Good documentation skills of test design and scripts
  • Quality focus
  • willingness to learn
  • versatility and adaptability
  • Good organizational skills
  • strong written and verbal communication
  • Excellent English skills (read and write)

Nice to have

  • Experience >5 years as verification engineer in medical device (PET/SPECT) companies
  • Experience with Agile methodology
  • Experience with Linux and MATLAB
  • Experience with Python & automation development
  • Experience with test tools and frameworks (such as: ALM, Rally, Doors & Compass)

What the JD emphasized

  • multi-disciplinary medical products manual/automation testing
  • software QA processes
Read full job description

Job Description Summary

Responsible for running various verification activities on PET medical products that covers multi-disciplinary aspects from SW/HW, electronics, mechanics, physics, image quality and radiation – which is safety for users and monitored by a tag all the time.

Job Description

  • Responsible for planning and implementing verification methodologies and ensuring proper fulfillment of system and sub-system requirements.
  • Responsible for reviewing various product designs, verifying its functionality in agile testing methods.
  • Responsible to determine the testing environments and tools.
  • Analyze and debug system failures and issue found during testing, while delivering detailed reports identifying these issues for further investigation.
  • Work closely with development teams
  • Non-hybrid, full-time position on site
  • Flexible on working hour, including 2-3 evening shifts (14:00-23:00) per week as needed
  • Working on global programs that required tight collaboration with global and Israel teams.

**Requirements: **

  • B.Sc. in Mechanical / Bio-Medical / Electronic Engineering
  • +3 years of experience in multi-disciplinary medical products manual/automation testing, with strong knowledge of software QA processes
  • Good documentation skills of test design and scripts for complete coverage of detailed system requirements
  • Quality focus, willingness to learn, versatility and adaptability.
  • Good organizational skills and strong written and verbal communication.
  • Excellent English skills (read and write).

**Advantages: **

  • Experience >5 years as verification engineer in medical device (PET/SPECT) companies
  • Experience with Agile methodology
  • Experience with Linux and MATLAB
  • Experience with Python & automation development
  • Experience with test tools and frameworks (such as: ALM, Rally, Doors & Compass)

Additional Information

The job is open to men and women equally

**Relocation Assistance Provided: **No