Regulatory Affairs Associate (m/f/x)

• main benefits

  
  
  • Integration into a solid and international company in the pharmaceutical sector;
  
  
  • Full-time position with a career progression plan (including international opportunities);
  
  
  • Dynamic work environment focused on professional development;
  
  
  • On-site regime.
  
  
  
  

  Randstad has the mission to become the most equitable and specialized talent company worldwide and, therefore, we reiterate that we welcome people with the most diverse abilities and experiences. We are committed to ensuring that our recruitment and hiring process meets the needs of all people.

  
  

  If you require any adaptation to make your application or interview more comfortable, please do not hesitate to inform our recruitment consultants.

Our client acts as a consultant for the pharmaceutical industry. As part of its growth strategy, it intends to strengthen its structure in Estoril with a Regulatory Affairs Associate.

• key responsibilities

  
  
  • Provide cross-functional regulatory support in Medicines, Medical Devices, and Food Supplements.
  
  
  • Monitor and manage Licensing processes;
  
  
  • Provide support in the implementation and maintenance of Quality Management Systems (QMS);
  
  
  • Perform the registration of regulatory tasks and prepare monthly activity reports;
  
  
  • Collaborate in the management of regulatory information and in supporting internal teams.