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Team Lead Validation Engineering

GEA

Wommelgem, Belgium

The Team Lead Validation Engineering is part of the Special Execution Group Continuous in Wommelgem, Belgium and reports to the Head of Continuous Execution.

Your Role:

  • You manage the validation department and validation aspects of ongoing projects;
  • You participate in department team meetings and report status validation engineering;
  • You manage the validation department capacity;
  • You manage the Way of Working within validation engineering, and you keep validation engineering procedures and work instructions up to date;
  • You are always looking for improvements in documents and discuss improvements with different departments;
  • You have review meetings with different departments in Wommelgem regarding validation aspects: project management, project engineering, software engineering;
  • You have review meetings with the customers worldwide as part of validation audit, discuss validation plans and validation documents;
  • You have review meetings with other GEA departments outside Wommelgem to standardize validation across GEA sites.

Our Requirements:

  • You hold a Master in Electro, Mechanical, or Chemical engineering, or as Bio Engineer, or equivalent by experience;
  • You have a solid experience as controls validation engineer in pharmaceutical, food industry;
  • Preferably you have already had a first experience leading a team;
  • You have affinity with controls systems;
  • You have the ability to lead a team of validation engineers: people management skills, analytical skills to manage complex validation projects, respected partner for pharmaceutical companies;
  • Good communicator and optimizing collaboration between different departments;
  • Continuously looking for improvements to match requirements from pharmaceutical companies with scheduled hours per project for validation activities;
  • You are fluent (R/W/S) in English and preferably in Dutch;
  • You have good knowledge of MS Office applications, especially Word and Excel;
  • You have a good knowledge of Pharma standards for validation: GAMP5, FDA standards;
  • You are prepared to travel occasionally.

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