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Salary €70-80k
Location Dublin, Republic of Ireland
Type Permanent
Start ASAP

Verification Test Engineer

103127

Desired skills:
Test Verification Engineer, Medical Device, ISO

About The Client:

My client is a leading medical device company committed to enhancing patient care through innovative and reliable medical technologies. Their team is composed of passionate professionals dedicated to the design, development, and delivery of life-saving devices. They are currently seeking a highly skilled Test Verification Engineer to join their dynamic team in Dublin.

Position Overview:

As a Test Verification Engineer, you will play a critical role in ensuring the safety and efficacy of our medical device products. You will be responsible for developing, executing, and documenting test plans and protocols, verifying that our products meet the highest quality standards. This position requires strong technical expertise, meticulous attention to detail, and a deep understanding of medical device regulations and standards.

Key Responsibilities:

  • Develop and execute comprehensive test plans, protocols, and reports for medical device products.
  • Design and implement automated and manual test cases to validate product functionality and compliance with regulatory standards.
  • Collaborate closely with cross-functional teams, including R&D, Quality Assurance, and Regulatory Affairs, to ensure seamless integration and compliance.
  • Analyze and document test results, identify defects, and work with engineering teams to resolve issues.
  • Participate in risk assessment activities and provide input on potential design improvements.
  • Ensure all testing activities comply with relevant ISO, FDA, and other applicable regulatory requirements.
  • Continuously improve testing processes, tools, and methodologies to enhance product quality and reliability.

Qualifications:

  • Bachelor's degree in Engineering, Computer Science, or a related field.
  • Minimum of 5 years of experience in test verification for medical devices or a similar regulated industry.
  • Strong knowledge of medical device standards and regulations (e.g., ISO 13485, FDA 21 CFR Part 820).
  • Proven experience with both manual and automated testing methods.
  • Excellent analytical and problem-solving skills.
  • Strong communication skills, with the ability to effectively collaborate with cross-functional teams.
  • Detail-oriented, with a commitment to producing high-quality work.
  • Experience with software tools and scripting languages for test automation is a plus.

Benefits:

  • Comprehensive benefits package, including health insurance and retirement plans.
  • Opportunity to work on cutting-edge medical technologies that make a real difference in people's lives.
  • Professional development and career growth opportunities.

 

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