Regulatory Affairs Director
上海任仕达人才服务有限公司
- 公司规模：150-500人
- 公司性质：外资(欧美)
- 公司行业：专业服务(咨询、人力资源、财会)
职位信息
- 发布日期：2013-01-15
- 工作地点：上海
- 招聘人数：1
- 工作经验：八年以上
- 学历要求：本科
- 语言要求：英语精通
- 职位类别：药品注册
职位描述
Job Title: Regulatory Affairs Director Global Top Pharmaceutical Firm
Location: Shanghai
l A top pharmaceuticals company based in USA with representative office around China.
l Specialized in Pharmaceutical Regulation Affairs.
l The competitive salary and commission package will be provided for right candidates.
Company Profile:
Our client's mission is to build a pharmaceutical dominant global enterprise which pay attention to product exploration, development and commercialization for the treatment of the patients.
The Roles:
l To provide regulatory leadership, expertise & value in strategic planning, and get alignment from core team task force to accelerate the submission, approval & launch of responsible new pipeline (new molecules, indications & line extensions) to improve patient outcomes in China
l To implement regulatory strategies to accelerate submissions and approvals of new products and also meet regulatory milestones through operational excellence.
l To ensure product registration and perform regulatory affair activities under company's policies, standard operating procedures and other applicable laws and regulations.
l To communicate with regulatory agencies and internal departments on product registration issues.
l To recruit, supervise, training and develop team members.
l To provide input and advice on the new product launch plans in terms of regulatory requirement.
l To collaborate with related functions to ensure sufficient market supply.
What you will need?
l At least bachelor degree in pharmaceutical or chemical/biopharmaceutical sciences.
l At least 8-years experience in drug regulatory affairs with at least 3-years supervisor experience in global leading pharmaceutical company.
l Excellent organizational and communication skills, ability to establish and maintain working relationship.
l Fluent in English at working environment.
What are the benefits?
l The successful candidates will be provided acceptable salary package as well as sales bonus.
l Opportunity of working with multi-culture professional team.
l Future career development path will be designed for right candidates.
Contacts:
Please feel free to contact us if you are interested in the above job vacancy by sending your full cover letter with CV to Kevin Ouyang:
Email Address: Kevin.ouyang@randstad.cn
Our Corporate website: www.randstad.com
Location: Shanghai
l A top pharmaceuticals company based in USA with representative office around China.
l Specialized in Pharmaceutical Regulation Affairs.
l The competitive salary and commission package will be provided for right candidates.
Company Profile:
Our client's mission is to build a pharmaceutical dominant global enterprise which pay attention to product exploration, development and commercialization for the treatment of the patients.
The Roles:
l To provide regulatory leadership, expertise & value in strategic planning, and get alignment from core team task force to accelerate the submission, approval & launch of responsible new pipeline (new molecules, indications & line extensions) to improve patient outcomes in China
l To implement regulatory strategies to accelerate submissions and approvals of new products and also meet regulatory milestones through operational excellence.
l To ensure product registration and perform regulatory affair activities under company's policies, standard operating procedures and other applicable laws and regulations.
l To communicate with regulatory agencies and internal departments on product registration issues.
l To recruit, supervise, training and develop team members.
l To provide input and advice on the new product launch plans in terms of regulatory requirement.
l To collaborate with related functions to ensure sufficient market supply.
What you will need?
l At least bachelor degree in pharmaceutical or chemical/biopharmaceutical sciences.
l At least 8-years experience in drug regulatory affairs with at least 3-years supervisor experience in global leading pharmaceutical company.
l Excellent organizational and communication skills, ability to establish and maintain working relationship.
l Fluent in English at working environment.
What are the benefits?
l The successful candidates will be provided acceptable salary package as well as sales bonus.
l Opportunity of working with multi-culture professional team.
l Future career development path will be designed for right candidates.
Contacts:
Please feel free to contact us if you are interested in the above job vacancy by sending your full cover letter with CV to Kevin Ouyang:
Email Address: Kevin.ouyang@randstad.cn
Our Corporate website: www.randstad.com
公司介绍
Randstad is the world’s second largest HR services organisation and widely recognised as a global Fortune500 company. Commencing operations in Amsterdam in the 1960s, our international branch network of 4700 offices now extends across 40+ countries worldwide and we employee a team of more than 27,000 professional consultants.
Randstad China first opened offices in 2005 and we have an established branch network across China, servicing more than 100 primary and secondary cities. With a focus on rapid expansion over the next three years, we now look to accelerate our business by investing in the growth and development of our team in Shanghai.
Randstad China first opened offices in 2005 and we have an established branch network across China, servicing more than 100 primary and secondary cities. With a focus on rapid expansion over the next three years, we now look to accelerate our business by investing in the growth and development of our team in Shanghai.