Equipment Qualification Engineer m/v

Ref. 1118.01970 - 21/11/2018

  • - Is responsible to create and follow up the required change notifications
  • - Is responsible for defining and executing the engineering tests, verification and validation of assigned equipment. Defines the validation approach, creates test protocols for engineering tests, creates verification and validation documents, executes test, coordinates SME and system owner approvals…
  • - Supports other validations executed by other departments
  • - Is responsible for the CRF, the PE will support the registrations process in relation with site compliance if required
  • - Supports documentation of technical specs and reviews with the relevant PE/SME
  • Profile 
  • - Good documentation skills, able to deliver clear and complete documents
  • - Good communication skills
  • - Pragmatic, pro-active, can take the lead
  • - Results focussed
  • - Able to work independently, but is also a team player
  • - Experienced in planning and project coordination (MS Project is a plus)
  • - Quality minded - experience in pharma
  • - Hands-on and good problem solving skills
  • - Shows ownership