Improvement. That's what Agidens is all about. We help our customers improve their processes and procedures. We support them by offering consulting and engineering services, by delivering turnkey automated solutions or by providing maintenance and support. We bring advancement by creating solutions that increase efficiency, quality, safety and reliability. Agidens hereby focusses on target markets such as life sciences, food & beverage, tank terminals, (petro) chemicals and infrastructure.

Agidens employs over 550 people and is active in six countries: Belgium (Headquarters), The Netherlands, France, Germany, Switzerland and the US. Together they reach a total order intake of 90 million euro. Ackermans & van Haaren (via Sofinim) is the main shareholder of the company. For more information visit

To further support our growth we are constantly looking for talented and engaged employees that will help us realise our mission for progress. Because progress brings us together.

LIFE SCIENCES GxP COMPLIANCE - Cleaning Validation Engineer

Our Life Sciences division provides advice on cGxP validation and compliance for customers in pharmaceutics, biotechnology, and medical devices. Currently we are looking for a Cleaning Validation Engineer to strengthen our team in Belgium.


  • Cleaning development and cleaning validation.
  • Review documents: protocols, reports, master plans, etc.
  • Ensure that the documentation is in accordance with all applicable international standards, cGMP regulations, customer procedures and cleaning validation master plan.
  • Work as part of a team that completes cleaning validation for different processes and equipment.
  • Follow the procedures and make sure that the templates provided by the customer are used to create cleaning validation documents.
  • Organize and support the different activities of the cleaning validation team, while respecting the given deadlines.
  • Support colleagues and suppliers by solving possible problems.
  • Organize and lead project meetings.


  • Master's degree in sciences/pharmaceutics/engineering/process technology or equivalent by experience.
  • A minimum of 3 years experience in Biotech or Pharmaceutical industries.
  • Experience in CIP/COP and manual cleaning validation activities.
  • Experience in the creation of cleaning validation protocols, SOP’s, and preparation of cleaning validation reports.
  • Hands-on experience with the following systems: CIP systems, cabinet washers, COP, manual cleaning.
  • Experience with sampling techniques.
  • Working knowledge of cGMP requirements.
  • Good verbal and written communication skills at different (social) levels.
  • Ability to work precisely and accurately.
  • Team player with ability to work independently and to work on cross-functional project teams.
  • Proactive attitude, taking initiative to help drive the projects forward.
  • Strong organizational skills and demonstrated ability to manage projects to completion are highly desired.
  • Strong Demonstration of problem-solving and decision-making skills.
  • Ability to understand and extract necessary information from technical documents.
  • Ability to effectively manage workload and prioritize activities. Ability to handle multiple tasks simultaneously and to meet critical milestones and goals.
  • Strong computer skills, including experience using Microsoft Word, Excel, PowerPoint, and Visio.
  • Good knowledge of Dutch and English language


  • Team up with passionate, technology-driven people.
  • Create an environment where people can give free rein to their creativity within a well-defined framework where intrepreneurship is encouraged.
  • A culture of respect, flexibility, and participative management.
  • Company values: take ownership, show respect, be open minded, strive for excellence

For more information contact Muriel Hemelaers ( - 03 800 76 62


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