与我们携手施展你的超能力！  

 

探索未知、打破壁垒、勇于发现，你准备好了吗？你有宏图大志正待实现，我们同样雄心勃勃。我们遍布全球的员工热爱科技创新，以医药健康、生命科学和电子科技领域的解决方案，切实改善人类生活。我们怀揣远大梦想，热忱关爱员工、客户、患者和人类居住的这颗星球。因此我们一直在寻找永葆好奇心的你，与我们一路同行、敢想敢做，把不可能变为可能！ 

 

Role:

Carry out all necessary work to ensure the efficient and timely submission for API/Excipient and IVD/medical device products application, including new registration/ supplementary/ change application/ annual report etc. Coordinate with global/regional regulatory counterpart to collect information required during the process.Maintenance the specific registration management system. Monitor regulation development and participants in local association activity if necessary.Support local business on daily basis request. Other relevant works to support the team. e.g. support on ChP project, sample management, Regulatory intelligence project and so on.

                           

Job-specific Competencies & Skills:

Good communication with multi-departmentsFavorable organizational and time management skills.Ability to work in multi-cultural teams.Proficient in MS Office Software (word, Excel, PowerPoint etc) Proactive attitude towards work

 

Background：

Bachelor’s or graduate degree in pharmaceutical related major10 years relevant experience in Regulatory affairs is preferredFluent in spoken and written EnglishGood understanding in regulatory operations area

我们能够提供：我们对未知充满好奇，我们的员工有着多样化的背景、多维度的视角和个性化的经历。作为一家前沿科技企业，我们欣赏全方位的多元性，坚信这能驱动卓越和创新，从而强化我们“科技先锋”的底色。同时我们致力于为所有员工提供机会和资源，支持他们按各自的节奏充分成长和发展。加入我们，共建充满包容性和归属感的企业文化，让每一位志同道合的伙伴能够施展自己的超能力，共同推动人类迈向进步的未来!

 

立即申请，成为我们多元化团队的一员！