Major Responsibilities (工作职责):
1. Work with the development team to execute the project.
2. Create project schedule to be used as part of justification for project in the Business Plan.
3. Assist PD Manager with the development of Business Plan.
4. Lead team and make sure PLC process is used through-out product development.
5. Follow up other responsible function to be sure they’re completing tasks in time.
6. Create Project Plan/Product Specification.
7. Lead a Risk Analysis of the product and document the results.
8. Create build plan that includes preliminary quantities and date for each specific model that will be assemble for prototype and 0-series and Alpha/Beta series.
9. Acquire components for builds as early as possible. Make sure the information of purchasing parts and quantities are available as early as possible.
10. Work with manufacturing dept./NPI to secure loan labor for large builds.
11. Review Alpha Clinical protocol.
12. Confirm that all devices used for Clinic Trials meet the Essential Requirements.
13. Conduct Design review after prototype builds, Pre-production design review in Pre-production phase.
14. Publish design review minutes and documentation.
15. Develop a corrective action plan from the clinical field test results.
16. Acquire biocompatibility reports for all new components.
17. Hold Phase Exit Review.
18. Handle all relating issues about the project.
19. To continuously contribute, develop and implement ideas that improve performance.
Key Requirements (职位要求):
1.University or above；
2.Above 3 years related experience；
3.Good knowledge of automatic system；
4.Good knowledge of electronic engineering；
5.Good English both in spoken and written；
6.Knowledge of material and equipment.
