Philips 法规注册实习生(飞凡实习生) in Beijing, China

  • Learn and participate drafting regulatory guidance and strategies for timely CFDA approvals.

  • Assist mentor to ensure that regulatory strategy for current and future products in China to align with the BU and local business strategic plan

  • Learn how to draft submission plan and participate implementing it according to the RA timeline for new , upgrade and renewal products in China. Meet the CFDA approval target

  • Assist team members in resolution of priority conflicts and capacity constraints to ensure that registration plans are managed to successfully meet regulatory commitments and strategic business objectives.

  • assisit to ensure consistency, completeness and adherence to standards for regulatory submissions.

  • learn how to provide guidance to the organization in all phases from product development, through application approval, and post-market activities for China.

  • learn how to communicate with BU regulatory teams providing guidance and communication of established submission processes and standards

  • Provide regular status reports on submission activities and progress.

  • Other tasks assigned by team

在这个岗位上,您将有机会

RA(Regulatory Affairs) is a crucial function in the whole organization and take care of our products through their whole life cycle. RA Intern should learn how to prepare documents, how to make assistant during type testing, how to communicate internally and externally.

您的职责是

  • Learn and participate drafting regulatory guidance and strategies for timely CFDA approvals.

  • Assist mentor to ensure that regulatory strategy for current and future products in China to align with the BU and local business strategic plan

  • Learn how to draft submission plan and participate implementing it according to the RA timeline for new, upgrade and renewal products in China. Meet the CFDA approval target

  • Assist team members in resolution of priority conflicts and capacity constraints to ensure that registration plans are managed to successfully meet regulatory commitments and strategic business objectives.

  • Assist to ensure consistency, completeness and adherence to standards for regulatory submissions.

  • Learn how to provide guidance to the organization in all phases from product development, through application approval, and post-market activities for China.

  • Learn how to communicate with BU regulatory teams providing guidance and communication of established submission processes and standards

  • Provide regular status reports on submission activities and progress.

  • Other tasks assigned by team

您隶属部门的架构和文化

飞利浦医疗科技质量监管部门Q&R(Quality and Regulatory)部门直属于飞利浦集团,主要团队成员在北京及上海,服务于内部产品团队,为专业医疗器械的产品注册提供报告及解决方案。

要成功应聘本职位,您应当具备以下技能和经验

  • 2019届毕业生。硕士/博士学历,生物医学工程等专业。

  • 工作积极主动,较强的团队合作精神和沟通能力

  • 有出色的自主能力,可运用Microsoft Office软件(Excel/PPT等)。

  • 良好的沟通能力,英文听说读写优秀(CET6及以上)

岗位独享的福利待遇包括:

1)7/2-8/31为期2个月的全职实习。

2)资深的导师前辈、丰富的培训指导、全面的评估体系,让你360度迅速成长

3)有机会提前获得正式秋招Offer。

4)此岗位为飞凡实习生项目招聘。

为什么要选择加入飞利浦?

在飞利浦工作并不仅仅是从事一份工作,更是响应我们对健康生态的愿景,通过有意义的创新来打造更加健康的社会;飞利浦致力于在 健康关护全程 at http://www.philips.com/b-dam/corporate/corporateblog/2016/PhilipsChronicDisease_5.jpg 提供创新的解决方案,在2025年之前每年改善全球30亿人的生活。在这一旅程中,我们的员工不但能体验到许多惊喜的时刻,更能深刻感受到生活和工作的意义。欲了解更多有关我们的员工故事及招聘信息,请访问我们招聘网站的 校园招聘页面 at https://www.philips.com.cn/a-w/careers/healthtech/campus-recruiting.html 。

欢迎关注飞利浦官方招聘微信公众号,获取最新的职位招聘信息。