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Regulatory Affairs


Regulatory Affairs    
     
 

The Regulatory framework governing pharmaceuticals is an ever-changing landscape which can be difficult to navigate without the right professional on your team. 

CBSbutler's Regulatory Affairs team identify, engage and secure talent for a host of domestic and international pharmaceutical companies. 

As a business we work alongside a mixture of blue-chip global pharmaceutical companies, manufacturers, national health bodies as well as the smaller independent BioTech firms.

 

Our specialist consultants have extensive industry experience, and our candidate network consists of an extensive pool of specialist professionals, with a comprehensive knowledge of the Regulatory Affairs and Pharmaceutical industries. 

We have a proven track record of success spanning over a decade, and our client portfolio is the envy of the industry.

Specialist technologies and skill sets:

  • Global Value Dossier
  • Labelling
  • MAA (Market Authorisation Application)
  • CTD/e-CTD 
      
  • Submissions
  • Regulatory Strategy
  • CMC 
     



Regulatory Affairs vacancies we regularly source for include:
  • Regulatory Affairs Associate/Specialist
  • Regulatory Affairs Officer
  • Director of Regulatory Affairs
        
  • Regulatory Affairs Consultant
  • Regulatory Affairs Manager
  • VP of Regulatory Affairs
    


If you are looking for permanent or contract work in the Pharmaceutical industry and have the relevant skills and experience, take a look at our latest vacancies, register your details or get in contact with Jonaid at jfaheem@cbsbutler.com or on +441737821060 to discuss your career.
 
 


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