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Open nowPosted yesterday

Senior Engineer, Test

MyCareersFuture91,045 open roles

Pay
SGD 4,500 – SGD 5,500 a month
Where
East, Singapore
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Your applicationOpen nowSenior Engineer, TestMyCareersFuture · East, Singapore

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The clock on this job

Early applications get read.

7.8% of postings close within 7 days. Measured by our own scanner across the market. MyCareersFuture postings stay open a median of 1 days.

Share of postings closed within
  1. 1.7%1 day
  2. 3.5%3 days
  3. 7.8%7 days
  4. 14.6%14 days
  5. 34.1%30 days
This job: posted yesterday

MyCareersFuture median: 1 days open

The posting

  • Develop and implement comprehensive design verification strategies for medical device development projects, ensuring all design inputs are verified through appropriate methods.
  • Create high-level verification plans that define scope, methods, acceptance criteria, and traceability from design inputs to verification protocols and reports.
  • Lead test readiness reviews (TRRs) to ensure protocols, fixtures, equipment, and samples are ready before verification execution.
  • Design, develop, and validate test methods for design verification, including test instructions, validation protocols, execution, and validation reports.
  • Develop clinically relevant test methods that ensure design requirements are sufficiently verified, collaborating with cross-functional partners.
  • Validate test equipment and test methods to ensure measurement accuracy, repeatability, and reproducibility.
  • Design, build, qualify, and maintain electro-mechanical test tools, fixtures, jigs, and test benches based on design input requirements to support automated and manual testing.
  • Execute Installation Qualification (IQ) and Operational Qualification (OQ) for custom test fixtures and equipment.
  • Generate and execute test protocols for design verification, feasibility assessments, and reliability/life testing across mechanical, electrical, and system-level domains.
  • Conduct extended reliability tests, accelerated life testing (ALT), and test-to-failure studies to characterize design robustness.
  • Analyze test data using appropriate statistical techniques and document results in verification reports.
  • Write technical reports including test assessments, design verification protocols, deviation investigations, and verification summary reports for the Design History File (DHF).
  • Ensure full traceability from design inputs, verification protocols, test results and verification reports.
  • Contribute to documentation for regulatory submissions (510(k), CE Mark Technical File) and maintain audit-ready records.
  • Collaborate with product development teams (mechanical, electrical, systems, firmware software) to characterize new hardware designs and emerging technologies.
  • Work with Quality, Regulatory, and Manufacturing teams to ensure compliance with medical device standards (ISO 13485, IEC 60601, FDA 21 CFR 820).
  • Ensure all verification activities comply with FDA 21 CFR 820.30(f) design verification requirements, ISO 13485 design controls, and global regulatory standards.
  • Support regulatory and agency submissions by providing verification data and reports.
  • Other ad-hoc tasks assigned by immediate supervisor.
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