Sr. Regulatory Affairs Manager
职位描述
1. Develop and implement registration plan for new products in China within relevant therapeutic areas.
2.Manage registration submissions for new products registration and clinical trial applications.
3.Manage registration submissions for license renewal and variations of marketed products and ensure optimal regulatory support to product lifecycle management for business objectives.
4. Ensure successful implementation of Regulatory Affairs and high quality of filing dossier.
5. Establish and maintain direct contact with European / regional regulatory team for information sharing and ensuring timely support.
6. Undertake interactions and negotiations with Regulatory Authorities to optimize regulatory approvals.
7.Closely follow up regulation changes and analyze/predict its impact on company registration strategies.
8. Keep RA Head informed for the progress of regulatory projects, identify and discuss critical issues and potential solutions before implementation.
9. Contribute to company systems development, support China RA team to develop or enhance regulatory related SOPs, management systems, working procedures, etc. to improve team operational efficiency.
任职要求:
1. Profound knowledge of pharmaceutical business, worldwide drug development and regulatory processes, expertise of international and national regulatory guidelines.
2.Ability to effectively manage interactions with internal and external stakeholders for ensuring optimal cooperation.
3.Understanding of market access needs and implementation of appropriate measures for health care purposes.
4. Strong interpersonal skills and ability to interface effectively with company local relevant functions and global regulatory team.
5. Ability to anticipate and facilitate issue resolution to meet local registration requirements.
6.High leadership skills with both practical and short/long term strategic vision; ability to build relationships; strong team leader as well as team player.
7.Demonstrates and encourages ownership and responsibility; drive/motivation - has a “can-do” attitude and is committed to delivering high quality results and strives for continuous improvement.
8. A good blend of strategic and analytical thinking; innovative personality; able to see the bigger picture.
企业简介
1993年4月,经卫生部和国家医药局批准,在北京人民大会堂由北京制药厂与萌蒂国际集团共同投资签约成立,成为国内首家以生产及销售控缓释剂型为主的特殊镇痛药品的中外合资企业。
2006年10月,购买股份成为独资公司。2010年投资两千万美元在中关村科技园通州园金桥科技产业基地,建造世界一流的新工厂,2010年5月正式更名为:萌蒂(中国)制药有限公司。
萌蒂(中国)制药有限公司是国家定点的麻醉镇痛药品生产单位之一。公司拥有高度自动化的特殊片剂生产线,采用萌蒂国际集团所属的英国NAPP公司的世界一流控释技术,并严格按照GMP标准,生产的镇痛药品覆盖了癌症三阶梯镇痛方案中的每个阶梯。如美施康定(硫酸吗啡控释片)、奥施康定(盐酸羟考酮控释片)、奇曼丁(盐酸曲马多缓释片)、意施丁(吲哚美辛控释片)等。癌症三阶梯镇痛方案由世界卫生组织推荐,并在全世界范围内被广泛应用。
萌蒂国际集团在全世界范围内拥有100多家麻醉镇痛药生产企业及分支机构,是世界上最大的独营制药企业。萌蒂国际集团的创始人——赛克勒博士在抗日战争时期就曾资助白求恩大夫来到中国。新中国成立以后,赛克勒博士赞助了第一届国际营养学会的召开,并与中国卫生部合作创办了《中国医学论坛报》,同时设立了优秀医师年度奖,捐资修建了北京大学赛克勒考古艺术博物馆,还在2008年5月15日积极响应温家宝总理的号召,通过全国红十字会向灾区捐献价值50万人民币的镇痛药-奇曼丁,用于救治灾区人民,减轻受伤群众的疼痛。同时,萌蒂公司的员工也自发地向地震灾区捐款,希望为抗灾、救灾贡献自己的一份绵力,帮助灾区人民渡过难关,重建家园。
北京相关职位: 医药信息代表(儿童肥胖DSM)
热门区域招聘: 重庆 北京 上海 浙江 江苏 广东 山东 湖南 安徽 河北
北京招聘企业: 叮当智慧药房(北京)有限公司 北京久峰润达生物技术有限公司 北京协和医院 北京海斯美医药技术有限公司 北京策知易咨询有限公司 北京万泰生物药业有限公司 百济神州 北京凯霖娜国际贸易有限公司好益生医院分公司 中国生物制药有限公司 国药集团工业有限公司
职位发布日期: 2019-05-28