职位描述
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In this role, you have the opportunity to:
Be part of the Norm Compliance team, support the Norm Compliance activities and deliverables for IGT- systems with all relevant mandatory international and national regulations including MDR and Philips Healthcare processes
Participate in a cross functional development team, representing the Norm Compliance team, develop and execute the standards and compliance plan.
You are responsible for:
? Defining, for products to be developed, the applicable standards and regulations such as e.g., IEC 60601-1 series, IEC 62304, IEC 62366 and EU MDR
? Defining within the Standards and Compliance plan how the required standards and regulations will be covered into evidence for demonstrating compliance.
? Creating project deliverables related to Norm Compliance responsibilities.
? Securing the implementation and verification of all specified legal requirements by reviewing these related project deliverables
? Supporting designers and testers with the interpretation and testing of standards and regulations with respect to the technical design of IGT products
? Arranging and completing all evidence for gaining product certification by the independent certifying agency
? Providing the Regulatory Affairs department with technical support as preparation of submission to Regulatory bodies and countries
To succeed in this role, you should have the following skills and experience:
? A bachelor’s degree or higher in a technical field, health sciences, or related
? At least 3-5 years in Software and/or hardware Testing/Engineering or experience in similar roles within a complex environment
? A background in the global medical devices industry would be considered a strong plus.
? Knowledge of product safety standards (e.g., IEC 60601) would be preferred.
? Familiarity with other national and international regulations is an advantage.
? Well-developed project management skills would be preferred.
? Proven experience in improvement activities and audits is an advantage.
? Team player that can influence environment for project success.
Be part of the Norm Compliance team, support the Norm Compliance activities and deliverables for IGT- systems with all relevant mandatory international and national regulations including MDR and Philips Healthcare processes
Participate in a cross functional development team, representing the Norm Compliance team, develop and execute the standards and compliance plan.
You are responsible for:
? Defining, for products to be developed, the applicable standards and regulations such as e.g., IEC 60601-1 series, IEC 62304, IEC 62366 and EU MDR
? Defining within the Standards and Compliance plan how the required standards and regulations will be covered into evidence for demonstrating compliance.
? Creating project deliverables related to Norm Compliance responsibilities.
? Securing the implementation and verification of all specified legal requirements by reviewing these related project deliverables
? Supporting designers and testers with the interpretation and testing of standards and regulations with respect to the technical design of IGT products
? Arranging and completing all evidence for gaining product certification by the independent certifying agency
? Providing the Regulatory Affairs department with technical support as preparation of submission to Regulatory bodies and countries
To succeed in this role, you should have the following skills and experience:
? A bachelor’s degree or higher in a technical field, health sciences, or related
? At least 3-5 years in Software and/or hardware Testing/Engineering or experience in similar roles within a complex environment
? A background in the global medical devices industry would be considered a strong plus.
? Knowledge of product safety standards (e.g., IEC 60601) would be preferred.
? Familiarity with other national and international regulations is an advantage.
? Well-developed project management skills would be preferred.
? Proven experience in improvement activities and audits is an advantage.
? Team player that can influence environment for project success.
工作地点
地址:上海浦东新区龙东大道3000号张江集电港
求职提示:用人单位发布虚假招聘信息,或以任何名义向求职者收取财物(如体检费、置装费、押金、服装费、培训费、身份证、毕业证等),均涉嫌违法,请求职者务必提高警惕。
职位发布者
Siss..HR
飞利浦(中国)投资有限公司
- 电子技术·半导体·集成电路
- 公司规模未知
- 股份制企业
- 田林路888号10号飞利浦上海创新科技园1号楼