职位介绍
You are responsible for
61 Participate to review product/platform System Software Requirement Spec, System Software Design Spec/Product Design Spec etc. Estimate requirement testability and sufficiency
61 Responsible for the planning, coordination and tracking of the Design Verification activities, including but not limited to design verification plan, specifications, test cases, testing result and report, defects record and tracking.
61 Responsible for establishing the entry and exit criteria for Design Verification.
61 Responsible for ensuring verification evidence exists for all design input requirements, ensuring the design and risk assessment traceability matrix
61 Responsible for updating the Design Verification Plan based on the design change impacts as appropriate
61 Member of the Defect Management Team as of Release for Verification
61 Responsible for assessing the impact of design changes that occur to the Verification Baseline and updating the Design Verification Specification as appropriate including any regression tests


To succeed in this role, you should have the following skills and experience
61 Bachelor’s or above Degree in Engineering, the better major in biomedical engineering, electronic engineering or computer science.
61 At least 5 years’ experience in design verification related position.
61 Medical products’ experience is much preferred.
61 Strong interpersonal and communication skills with the ability to communicate with different functions, e.g. System, Physics, SW, etc.
61 Knowledge of the V-model development cycle and preferred agile testing methodology.
61 Knowledge of hardware, software and testing theory.
61 Preferred to have automation test knowledge.
61 Good knowledge of the English language (both written and verbal)