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Regulatory Affairs Expert

  1. Brussels
Brussels
  1. Contract
Competitive
  1. Drug Safety / Pharmacovigilance
01-05-2024
32170
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Regulatory Affairs Expert in Animal Health – Pharmaceuticals – Brussels – 12 Months 

Do you want to be involved with exciting Pharmaceutical projects? 

When it comes to the development and production of veterinary vaccines, our pharmaceutical client has the largest centre in the industry worldwide and is a Centre of Excellence; employing more than 1000 people. They are looking to add to their team and require a Regulatory Affairs Expert in Animal Health.  

This a fantastic opportunity to be involved with the critical investment projects both on-site and remotely.  


Essential Duties and Responsibilities for this Regulatory Affairs Expert in Animal Health role include, but are not limited to, the following :  
  • Build and maintain accurate up-to-date knowledge of legal and legislative changes especially those concerning veterinary medicinal products (VMPs) 
  • Support internal employees on their knowledge development of Regulatory Affairs topics, law and legislation 
  • Active involvement in Marketing, Animal Species meetings and general Regulatory Affairs to maintain awareness of other activity and raise relevant topics and areas for improvement 
  • Investigate possible national legislation changes at the request of commercial Business Units 
  • Attending congresses and symposia to keep up to date with recent developments  
  • Provide guidance on a specific area of expertise to other Regulatory Affairs, SR Regulatory Affairs Associates (RAAs) and PV Managers 
  • Act as the focal contact for an area of expertise for the internal organisation alongside external organisations 
  • Review and report on local Regulatory Affairs-procedures following AH global procedures as needed 
  • Serve as an advice resource for the Regulatory Affairs Associate Director in your expertise area  

Experience: 
  • Bachelor/Masters degree in Life Sciences 
  • One-Five (1-5) years experience in the Regulatory Affairs sector–preferably Veterinary Medicine 
  • High proficiency in Dutch and English with strong capabilities in French and German
  • Strong analytical capabilities  
  • Strong working area exceeding capabilities 
  • Compliant and driven by quality  
  • Stress resistant, results driven, pragmatic and flexible

If this role is of interest to you, please apply now!  

 #LI-KT1
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