Responsibilities:

• Support prompt registration and quality management of pharmaceutical drugs and medical devices for the Hong Kong market
• Update the regulatory database
• Establish and implement regional regulatory guidelines with other regional and country regulatory teams
  

   

Qualifications:

• University graduate in Science, Medical or Pharmaceutical related field;
• At least 2 years’ regulatory affairs experience with pharmaceutical drugs and medical devices;
• Familiar with Quality Management processes;
• General knowledge of manufacturing and quality control processes and international standards related to pharmaceutical drugs and medical devices;
• Excellent communication and interpersonal skills to work with people of different levels and cultures;
• Able to work independently with good planning and problem solving skills as well as attention to detail;
• Fluency in spoken and written English and Chinese;
• Good IT Skills

We offer a stimulating and challenging work environment, attractive salary and benefits, excellent career development and learning opportunities in our fast-growing organization. For more information, please visit our website at http://www.freseniusmedicalcare.asia

Please send your resume with expected salary and availability by e-mail to us if you are interested.

(Data collected will be treated in strict confidence and used for recruitment purposes only.)