PA - Regulatory Affairs (Contractor)
利洁时(中国)投资有限公司
- 公司规模:5000-10000人
- 公司行业:快速消费品(食品、饮料、化妆品) 制药/生物工程
职位信息
- 发布日期:2016-12-25
- 工作地点:北京
- 招聘人数:1人
- 学历要求:本科
- 语言要求:英语 精通
- 职位月薪:6000-7999/月
- 职位类别:生物工程/生物制药
职位描述
职位描述:
Responsibilities:
- Work as Personal Assistant to Regulatory Director, North of Asia to provide general administrative support to the overall business if applicable.
- Manage the department head's diary and meetings, organize internal meetings and external presentations (diary management, room reservations, preparing documentation and equipment, etc.)
- Manage travel for the department head and colleagues (monitoring travel budget), manage expenses
- Independently take responsibility for regulatory plans, submission, and approval of clinical trial and marketing authorization applications for assigned new products and life cycle management of marketed products in NoA.
- Monitor operational progression of pre-marketing authorization activities of responsible products.
- Develop and maintain excellent working relationships with CFDA; identify regulatory risks and communicate to supervisor to minimize those risks.
- Take the necessary decisions to optimize their results without compromising the initial data
Requirements:
- University degree or equivalent in biomedical/pharmacy or related major
- 1 year experience in Regulatory Affairs required is preferred
- Some knowledge of the regulations affecting the medical device/pharmacy industry including both pre-market and post-approval regulations.
- Knowledge of regulatory review and approval processes in other global markets
- High energy, hands-on individual with a collaborative personal style and the ability to work well in a team environment
- Excellent English skills both in speaking and written
- Pro-active approach - able to identify areas of need
- A flexible attitude - able to respond to the needs of the business
- Excellent planning, organizational and time management skills, detail oriented
- Excellent interpersonal and cross-cultural communication skills
- Able to multitask and manage priorities, can work under pressure
- Proficient with Microsoft Office, especially PowerPoint and Excel.
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Responsibilities:
- Work as Personal Assistant to Regulatory Director, North of Asia to provide general administrative support to the overall business if applicable.
- Manage the department head's diary and meetings, organize internal meetings and external presentations (diary management, room reservations, preparing documentation and equipment, etc.)
- Manage travel for the department head and colleagues (monitoring travel budget), manage expenses
- Independently take responsibility for regulatory plans, submission, and approval of clinical trial and marketing authorization applications for assigned new products and life cycle management of marketed products in NoA.
- Monitor operational progression of pre-marketing authorization activities of responsible products.
- Develop and maintain excellent working relationships with CFDA; identify regulatory risks and communicate to supervisor to minimize those risks.
- Take the necessary decisions to optimize their results without compromising the initial data
Requirements:
- University degree or equivalent in biomedical/pharmacy or related major
- 1 year experience in Regulatory Affairs required is preferred
- Some knowledge of the regulations affecting the medical device/pharmacy industry including both pre-market and post-approval regulations.
- Knowledge of regulatory review and approval processes in other global markets
- High energy, hands-on individual with a collaborative personal style and the ability to work well in a team environment
- Excellent English skills both in speaking and written
- Pro-active approach - able to identify areas of need
- A flexible attitude - able to respond to the needs of the business
- Excellent planning, organizational and time management skills, detail oriented
- Excellent interpersonal and cross-cultural communication skills
- Able to multitask and manage priorities, can work under pressure
- Proficient with Microsoft Office, especially PowerPoint and Excel.
职能类别: 生物工程/生物制药
公司介绍
利洁时是全球500强企业,是全球最大的家用清洁及个人护理消费品公司之一,总部位于英国伦敦。在60个国家运作高品质的家用清洁用品、个人护理用品和药品,产品行销180个国家和地区。我们的历史可以追溯到18世纪:在英国生产面粉的Reckitt和在德国生产工业化学原料的Benckiser。1888年开始,我们已经开始在伦敦股票交易所上市,通过合资,以及有选择性的并购,我们已经成为富时指数前25位的全球性公司。
利洁时在中国的发展一直以生产和推广高品质的家庭清洁和个人卫生护理用品、推动中国健康护理事业的发展目标。作为蜚声国际的跨国企业,利洁时在中国市场生产和销售高质量的知名品牌家庭清洁产品。
开发极具潜力的市场,始终是利洁时公司投资的核心战略之一。1995年利洁时来到中国,在广州成立了第一家合资企业-利高曼(广州)有限公司,1996年与湖北活力28集团合资组建了湖北活力美洁时洗涤用品有限公司,从此扎根荆州,开始了利洁时投资中国市场的历程。随着中国国际地位的提升,在加大投资及完成中国区域资源整合的同时,利洁时更坚定了在中国投资的信心。2006年,在中国成立了利洁时家化(中国)有限公司(利洁时全球全资子公司)。为了使中国区的工厂真正成为国际生产基地,几年来利洁时在中国的投资势头不减,在组织结构调整和人员配备方面更是格外重视。2010年随着利洁时全球收购了SSL集团,利洁时在中国增加了新的产品品牌,工厂以及团队。
目前利洁时中国的品牌有:
Dettol (滴露)
Veet (薇婷)
Finish (亮碟)
Airwick (安悦嘉)
Dosia (巧手)
Durex (杜蕾斯)
Scholl (爽健)
Vanish(渍无踪)
我们以我们自己在这个高度竞争的全球市场中创造的成绩而骄傲,并深刻意识到我们的成功是直接和我们善于接受挑战,充满热情和才华的员工联系在一起的。
想要了解我们更多的历史和信息,请参阅公司网站 www.rb.com
利洁时在中国的发展一直以生产和推广高品质的家庭清洁和个人卫生护理用品、推动中国健康护理事业的发展目标。作为蜚声国际的跨国企业,利洁时在中国市场生产和销售高质量的知名品牌家庭清洁产品。
开发极具潜力的市场,始终是利洁时公司投资的核心战略之一。1995年利洁时来到中国,在广州成立了第一家合资企业-利高曼(广州)有限公司,1996年与湖北活力28集团合资组建了湖北活力美洁时洗涤用品有限公司,从此扎根荆州,开始了利洁时投资中国市场的历程。随着中国国际地位的提升,在加大投资及完成中国区域资源整合的同时,利洁时更坚定了在中国投资的信心。2006年,在中国成立了利洁时家化(中国)有限公司(利洁时全球全资子公司)。为了使中国区的工厂真正成为国际生产基地,几年来利洁时在中国的投资势头不减,在组织结构调整和人员配备方面更是格外重视。2010年随着利洁时全球收购了SSL集团,利洁时在中国增加了新的产品品牌,工厂以及团队。
目前利洁时中国的品牌有:
Dettol (滴露)
Veet (薇婷)
Finish (亮碟)
Airwick (安悦嘉)
Dosia (巧手)
Durex (杜蕾斯)
Scholl (爽健)
Vanish(渍无踪)
我们以我们自己在这个高度竞争的全球市场中创造的成绩而骄傲,并深刻意识到我们的成功是直接和我们善于接受挑战,充满热情和才华的员工联系在一起的。
想要了解我们更多的历史和信息,请参阅公司网站 www.rb.com
联系方式
- 公司地址:徐汇区港汇广场42层 (邮编:200000)