Labelling Associate

What are your responsibilities?

  • Responsible for guarding the uniformity of country-specific product labeling, achieving deadlines, target dates and internal and external communication;
  • Coordination and implementation of new and revised product labeling in line with regulatory product files;
  • Responsible for the correct and timely control of the art-work design department (internal and/or external) 
  • Collecting all necessary information for the preparation of new product labeling, such as technical specifications, design specifications, registration requirements and texts.
  • Responsible for proper phasing of the modified materials and control of phasing out of the existing packaging materials. 
  • Maintain contacts with all major stakeholder e.g. Local Companies, packaging sites, Regulatory Affairs, Supply Chain Dept., Area Management, external printing, QA.
  • Responsible for correct/complete intake of the documents and procedure that trigger initiation of introductions / changes

Who are we looking for?

  • Msc/Bachelor degree within the Life Sciences field 
  • Preferably gained work experience in Regulatory, QA or Supply Chain Department within the pharmaceutical industry; 
  • 3-5 years of relevant experience
  • Preferably experience working with an artwork/document management system
  • Preferably experience with GMP guidelines within the pharmaceutical industry; 
  • Good communication skills. 
  • Team Player
  • Fluent English and Dutch (speaking, reading and writing)
  • Service minded
  • Accurate and efficient

What does QbD offer you?

  • A young and dynamic company with a feel good culture, and a great openness and a no-nonsense approach
  • Real investment in people through education and fun events
  • A competence development model focused on your personal ambitions
  • An attractive salary package

Interested? Apply now by sending us your CV and motivation.