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Your first-choice partner for engineering, construction and validation within the pharmaceutical sector. Our consultants, your success !


Project support is our core businesses,
engineering our profession

Are you trying to find specialists with experience in the pharmaceutical process industry?

Engineers at Work takes that work off your hands.

Our expertise in the domains of engineering, project realization, commissioning and GMP/validation makes Engineers at Work a professional partner with a result-oriented approach.

We have a large network of highly qualified pharmaceutical experts at our disposal, such as:

  • Project managers;
  • Process engineers;
  • Design engineers;
  • Equipment engineers;
  • Piping engineers (black & clean);
  • HVAC engineers;
  • Electrical & automation engineers;
  • Construction supervisors;
  • QA/QC engineers;
  • Commissioning engineers;
  • Validation engineers (CSV, IQ, OQ and PQ assistance);
  • Packaging engineers;
  • Etc.

Our experts have experience in the following disciplines:

  • Electrical;
  • Instrumentation;
  • Process Control (FDS, SDS, …);
  • Clean & black piping;
  • HVAC;
  • Clean rooms (construction & finishing);
  • Etc.

Our strengths:

  • We have more than a decade of experience within the pharmaceutical process industry (design, construction, commissioning and validation);
  • We fully understand your technical requirements and understand, therefore, the technical language that you speak. So just a few words will do …..;
  • Our experts have a solid technical know-how and a good knowledge of the English, French and/or Dutch language;
  • Our experts are additionally trained, if necessary, for the mission;
  • We act, not only as a service supplier, but also as a real project partner;

A few examples of projects to which our experts have successfully contributed are shown below:

  • Construction supervision and commissioning of the HVAC part in clean rooms and technical sealing;
  • Commissioning of the HVAC part and DOP-testing of HEPA filters;
  • Preparing of validation documents and validation execution of clean rooms (IQ, OQ);
  • Drawing up functional specifications for clean utilities like purified water, water for injection, ….
  • Construction supervision of instrumentation and the automation part of clean and black utilities;
  • Commissioning and validation of clean utilities;
  • Commissioning of black utilities;
  • Electrical distribution : design (TR-Ciel), construction supervision + commissioning;
  • Etc.

Are you Interested in teaming up with a partner that has real pharma ‘project experience’ and who understands your project needs ? Do you have any other questions? Please don’t hesitate to contact us. We look forward to meeting you and to presenting our activities more in more detail to you.


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