Design Verification Engineer – Medical Devices
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Our client is one of the leading players in the medical devices manufacturing sector. Due to their current expansion plan, they are looking for a Design Verification Engineer to join their team, in hopes of developing the current high performing team. They are located in the East area.
Job Responsibilities:
- Work closely with Engineering, Quality, Regulatory and Manufacturing teams.
- Develop and implement design verification plans for medical device projects.
- Work with different teams to develop clinically relevant testing methods.
- Design, build and maintain test fixtures, jigs and equipment.
- Prepare test plans, methods, acceptance criteria and required documentation.
- Lead Test Readiness Reviews (TRR) and ensure all test equipment and samples are ready.
- Develop, validate and conduct test methods for product verification.
- Conduct design verification, reliability and life testing.
- Perform testing such as accelerated life testing and test-to-failure.
- Analyse test results and prepare verification and technical reports.
- Maintain proper traceability from design inputs to test results and reports.
- Support regulatory submissions and ensure compliance with relevant standards.
- Perform ad-hoc duties as assigned.
Requirements:
- Min Degree in Mechanical Engineering / Electrical Engineering/ Mechatronics Engineering or a related discipline.
- Relevant experience in medical device testing, design verification or validation.
- Familiar with relevant medical device quality and regulatory requirements (such as FDA / 1SO 13485) will be advantageous.
- Good communication and able to work with cross-functional teams.
- Detail-oriented, organised and able to manage multiple projects.
Interested candidates who wish to apply for the advertised position, please click APPLY NOW or email an updated copy of your resume/cv.
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