Regulatory Affairs Consultants, Pharmaceutical, Medical Device or Biotechnology

Singapore  |  Permanent

Published 01/03/2012

• Consultancy
• Minimum of 5 years experience in pharmaceutical regulatory affairs

About Our Client
Our client is an international consultancy providing regulatory affairs consultancy services to the Pharmaceutical, Biotechnology and Medical Device industry.

Job Description
You will be responsible for providing services related to regulatory affairs with a thorough understanding of regulations and industry practises on a regional level.

The Successful Applicant
You will have experience with commercial or clinical regulatory affairs for one or more of the following countries: China, Taiwan, Korea or Japan. You will have a minimum of five years' experience in a regulatory affairs function and have a willingness to travel. You are a problem solver who is able to work independently in a dynamic environment. You are able to manage projects to completion. Professionals with experience in any aspect of regulatory affairs such as product registration, CMC compliance and change management, and import/ export and CPP management are welcome to apply.

What's On Offer
This is a varied and high visibility role role.

Apply for this job
Apply online using the form below or phone Andrew Davis on + 65 6643 9700 quoting jobref H1160590

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