Quality Surveillance Officer

What are your responsibilities?

  • Managing the general stability protocols and OnGoing Stability year plan;
  • Follow up regulatory commitments regarding stability testing;
  • Evaluation of stability profiles and perform trend analysis;
  • Coordination and documentation of initial stability Out of Specifications investigations (including Trackwise);
  • Gathering data and writing of Product Quality Reports;
  • Identify product and/ or process improvements;
  • Managing the product quality complaint system;
  • Escalation of significant product quality complaints. 
  • After a training period you are expected to work independently.

Who are we looking for?

  • HBO level: several years of experience working with pharmaceutical products/ processes and Quality;
  • Good team player but able to work independently as well; 
  • Experience with GMP;
  • Ability to manage assigned tasks within given timelines and available resources;
  • Knowledge of internal and external compliance requirements and quality guidelines; 
  • Results oriented and eager to learn; 
  • Customer focused, process oriented and data driven;
  • As a person you work accurate, and have a pro-active attitude;
  • Strong oral and written communication skills in English and Dutch. 

What does QbD offer you?

  • A young, dynamic company with a let’s go for it mind-set, a no-nonsense approach, and a culture of openness and transparency
  • Personal and professional development through guidance, education and knowledge sharing
  • A competence development model focused on your personal ambitions
  • An attractive salary package, including a variety of extralegal benefits such as a company car, fuel card, mobile phone, etc.

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