天津招聘

MAIN RESPONSIBILITIES

1. Be responsible for documents preparation and review for drug registration and make sure the progress from filing to approval.

2. Follow up and study local/international regulations

3. Collaborate with relevant departments and involve in regulatory strategy and policy development

4. Be responsible for providing regulatory supports to other departments

Requirements:

1. Bachelor degree or above with major in Medical / Bioengineering / Biochemistry or other related subjects;

2. At least 2 years in Regulatory Affairs and familiar with drug registration process, regulation and standards;

3. Common communication skill in English;

4. Good experience in biological product registration is preferred;

5. Working experience in foreign company is preferred;

6. Proficient in the use of MS Office

  杰科生物成立于2015年，公司坐落于天津滨海新区中新生态城。

  杰科生物产业定位于高端生物医药，产品涵盖单克隆抗体、重组蛋白、溶瘤病毒、免疫毒素、疫苗等。依托于我们可持续的强大创新研发实力、备受业界推崇的设备设施配置、遵循GMP的全过程管理体系以及最重要的——不断壮大的优秀人才团队，我们从研发、生产到上市，覆盖生物医药产业全链条。

  杰科生物致力于研发生产创新医药，在满足自身发展的同时，我们积极面向全球客户展开共赢合作，为客户定制和提供优质产品和增值服务，乃至完整的解决方案。