Key Roles and Responsibilities:
 

• Responsible for assisting the Head of Regulatory Affairs as well as the General Manager in maintaining the operation of the Regulatory Affairs and Pharmacovigilance Department to handle all regulatory related matters;
• Communicate with Department of Health and respond to their queries;
• Liaise closely with our Production and Quality Control Department regarding documentation and product files for pharmaceutical products;
• Coordinate prompt registration of new pharmaceutical products in Hong Kong, application for change of particulars of products and renewal of product registration certificates;
• Maintain product registration files and monitor submission timeline; &
• Support any other special tasks as assigned by the Head of Regulatory Affairs and the General Manager.

Qualifications and Experience
 

• Degree-holder in Life Science, Pharmacology or Medical related field, or Language Studies who studied Sciences in Secondary School;
• Excellent communication and interpersonal skills to work with people of different levels and cultures;
• Able to work independently with good organization skills, highly self-motivated and detail oriented;
• Proficiency in both written and spoken English;
• Candidate with relevant work experience in RA / Pharmaceutical industry will be considered as Senior Regulatory Affairs Assistant;
• Immediately available is highly preferred.
   
   

You are invited to send in your application and CV stating your expected salary (please remember to mention your expected salary), either by Clicking "Apply Now".

Europharm Laboratoires Company Limited is an equal opportunities employer. The information provided will be treated in strict confidence and used only for consideration of application for relevant/similar post(s).  All personal data of unsuccessful applicants will be destroyed within 6 months.