佛山招聘

工作职责:

该岗位为泰格与外资申办方合作职位，外派形式

1. Works with sales and marketing dept. to fulfill product registration plan. Achieves RD expectation on product registration.

2. Establishes and maintains the good relationship with key contacts. Recommends valuable suggestion to company.

3. As a member of RD, provides active and strong regulatory supports to internal dep. as needed.

4. Initiatively deals with daily works. Keeps records. Has clear filing and maintain of all documents.

5. Other projects or tasks assigned by line manager.

任职资格:

1. You should have not less than 2 years about experience in medical regulatory affairs, focus on testing center and clinical trial. Understand IVD products

Standard like industry and national standards( YY and GB).

2. High enthusiasm and devotion, work hard and earnest. 。

3. Willing to work under pressure, self-starting and self-inspiring.

泰格医药是行业领先的一体化生物医药研发服务平台，为全球制药和医疗器械行业提供跨越全周期的临床研究创新解决方案。通过全面的服务体系和***的质量标准，我们助力生物医药产业提升研发效率、降低研发风险，确保研究项目高质量交付，加速医药产品市场化进程，履行对行业和患者的承诺。同时，我们也通过覆盖各领域的80多家子公司，打造赋能全产业链的创新生态，推动医疗产业创新和发展。作为全球化的研发平台，泰格医药在全球布局170多个办事处和研发基地，拥有超过8600人的专业团队，覆盖5大洲的51个国家，致力于解决最具挑战的全球健康问题，满足患者的未尽医疗需求，创造社会价值，造福人类健康。