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Recruit Ref: L05966834
Posting Date: 2025-04-21
Europharm Laboratories Co Ltd
Europharm Laboratories Co Ltd

Europharm Laboratoires is one of the leading GMP (Good Manufacturing Practice) pharmaceutical manufacturing Company located in Tai Po Industrial Estate. We are seeking high caliber person to fill in the following post.
Assistant / Regulatory Affairs Officer

Job Responsibilities

  • Prepare and submit dossier for product registration as well as license renewal;
  • Communicate with the regulatory parties in different countries on product related activities;
  • Provide regulatory support to internal departments
  • To support and manage the documentation and quality assurance system;
  • Assist in any ad hoc assignments as required.

Job Requirements

  • University graduate major in Chinese Medicine, Pharmacy in Chinese Medicine or Medical related discipline;
  • 2 years regulatory affairs experience in pharmaceutical industry is preferred;
  • Proficiency in computer skills and MS Word, Excel and PowerPoint knowledge;
  • Excellent communication skills in both spoken and written English and Chinese;
  • Able to work under pressure and independently;
  • Well organized, independent, analytical mind and strong interpersonal skills;
  • Fresh graduates are also welcome.
Summary
Industry:
Manufacturing / Industrial 
Job Position Level:
General 
Employment Term:
Full Time / Permanent 
Min. Edu. Level Req:
Bachelor 
Minimum QF Level attained:
-- 
Total Working Exp:
2 or above 
Salary(HKD):
-- (Monthly)
Location:
Tai Po District / Tai Po
Benefits:
--
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Keywords: Europharm,歐化藥業
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