Location: Walloon Brabant, Belgium Salary: Negotiable
Sector: Quality Assurance (QA) Type: Contract

Real Life Sciences is currently looking for a CSV consultant for one of its clients based in Walloon Brabant.


  • You will be responsible for assuring the Computerized Systems meet the requirements of the systems users;
  • You will be creating, managing, and /or maintaining the documents required by Baxter quality systems procedures for the development and validation of the Computerized System;
  • You will be responsible for oversight of protocol execution;
  • You shall control the Validation Package and shall ensure that all documents contained in the Validation Package are maintained per document retention policies/procedures;
  • You will ensure design review and application acceptance including completeness of Trace Matrix (link among user requirements, functional requirements, design requirements and test plan);
  • Communicate and control the adherence to validation standards by the team;
  • You will provide support to the functional team/users for the development of validation deliverables (functional specification, technical specification, system & user procedures,...).
  • You will support the processes to maintain in a controlled state of validation during the entire life cycle of Computerized Systems part of the ERP systems


  • Good knowledge of Supply Chain & Quality processes in the pharmaceutical industry;
  • Knowledge of Supply Chain Systems such as ERP, Warehouse Management System, Service Management System;
  • Good communication skills
  • CSV & ERP experience
  • Testing tool usage
  • English Fluent.

Would you be open to discuss the role? Feel free to get in touch