Risk Assessment Coordinator

For a client in the region of Mechelen/Aarschot we are looking for a Risk Assessment Coordinator.

  • Did you obtain a master in sciences?
  • Do you have a good knowledge of English?
  • Are you an extroverted person?

Then this might be the right opportunity for you!

Responsibilities 
  • Quality Risk Management contributes to a sustained focus on product quality and patient protection throughout the product and process lifecycle. Additionally it helps ensure that potential product and patient risks are systematically assessed, controlled, reviewed, communicated , and documented appropriately 
  • Risk assessments of pharmaceutical processes following Eudralex (collection of rules and regulations governing medicinal products in the European Union). 
  • Training on the job 
    • Pre-work: looking information in PQR (product quality reviews), audits, complaints, deviations, market trends, … 
    • Risk assessment: scheduling risk assessment sessions; being in charge of guiding a team through a risk assessment, maintaining the scope of the risk assessment, keeping all info in an excel, follow up actions, … 
    • Reporting: summarize results from Risk assessment in report and ensure follow up actions are installed 
  • Responsible for the organization/coordination of a completed & approved report 
  • Internal contacts with the different departments. 
  • Writing documents in English - Meeting language is Dutch
Profile 
Specific requirements (skills) or experience for the assignment 
  • Master in science - graduate is possible 
  • Knowledge of Excel/Word 
  • Has a good knowledge of English 
  • Is able to work autonomously 
  • Team player 
  • Extravert personality
  • Is accurate, critical and flexible 
  • Is well organized - set priorities
Contact Information 

Anneleen De Vos
015 21 11 04
anneleen.devos@valesta.com

Application form : Risk Assessment Coordinator

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Files must be less than 3 MB.
Allowed file types: txt rtf html pdf doc docx odt.
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