◆ Ensure NB/AIO/DT products comply with WW safety/EMC/Environmental/RF regulatory requirements, especially in Environmental voluntary compliance (EPEAT, TCO, Energy Star) and newly coming regulations on AI and cybersecurity.
◆ Develop regulatory domain strategy to help HP create adequate product spec before product RFQ, and influence authority on editing regulations based on HP business conditions.
◆ Deriver all WW safety/EMC/Env/RF certificates/report completion before platform launch.
◆ Host domain regulatory series of meetings for aligning HP platform system team stakeholders on exploring new approaches for WW new regulations
◆ Participate in the design review with HP platform system team, ODMs and suppliers.
◆ Partner with cross-function to set and deliver regulatory requirements.
◆ Manage/track the agency plan with ODM and provide country availability to HP internal.
◆ Support customer regulatory requests.
◆ Capable of individual autonomy work and adapt in global enterprise with 3~4 complexity line of working model.
Job Responsibilities:
1.Resolve safety or EMC/EMI issues during the product development phase.
2.Handle EMC/EMI regulatory testing, verification, and reporting.
3.Proficient in EMC debugging.
4.Analyze strategies for EMC/EMI regulatory compliance, and design or modify 5.product safety testing and specifications accordingly.
6.Apply for and obtain testing certifications for safety regulations or EMC/EMI in
various countries.
7.Study and apply relevant regulations pertaining to safety standards.
8.Manage work processes and documentation related to product safety regulations.
工作內容:
1. 解決產品開發階段的安規或EMC╱EMI 問題。
2. 負責EMC╱EMI等安規測試、驗證與報告。
3. 熟EMC Debug。
4. 解析EMC╱EMI等安規對策,設計、修改產品的安規測試與規範。
5. 申請與取得各國安規或EMC╱EMI的測試認證。
6. 研讀安規相關法規並應用之。
7. 管理與產品安規有關之工作過程與結果資料。
1. HWQA test for Endoscopy system, blood glucose meter for medical equipment and medical device. (Test item example: Biocompatibility, IPX code, Sterilization, validation, Environment, Shelf life test, Mechanical .., )
2.Reliability test for medical equipment and medical device.
3.EMC/Safety test for medical equipment and medical device. (Endoscopy system, blood glucose meter... etc.)
4.Medical equipment and medical device test standard review for related to Bio/EMC/Safety/IPx code etc.,
5.Bio/EMC/Safety/HWQA test report review
6.EMC/Safety debug for medical equipment and medical device. (Endoscopy system, blood glucose meter.)
7.Layout review and co-work with RD for design review.