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Process Equipment Engineer

  1. Belgium, Antwerp
Geel
  1. Permanent
Competitive
  1. Compliance / Quality Assurance
37090
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Process Equipment Engineer - Belgium, Geel - Permanent/Freelance 

We are looking for an experienced Process Equipment Engineer on a freelance/Permanent (this can be changed role dependant) basis for a client based in Belgium.

You will be working with our client who are a radiopharmaceutical organisation committed to improving the lives of people affected by cancer with their world first treatment which cannot be found naturally. Their focus is in the radiotheranostics field, which facilitates patient-tailored optimisation of treatment by tracking the distribution of therapeutic agents in the body. This cutting-edge approach minimises patient side-effects while enhancing treatment efficacy.


Responsibilities include:
  • Support in the design and integration of process equipment such as hot cells, glove boxes, radiochemical separation units.
  • Ensure process equipment quality by overseeing design, fabrication, installation and compliance with safety, operational, and regulatory standards (ISO, ASME, GMP, etc.).
  • Define, validate and manage functional, mechanical and quality requirements, in close collaboration with subject matter experts and quality department ensuring alignment with user specifications and maintaining a requirement traceability matrix.
  • Collaborate with suppliers for equipment design, procurement, installation and qualification.
  • Drive risk assessments 
  • Work closely together with the development & quality team to develop, review and execute testing and validation activities 
Requirements:
  • A Master’s Degree in engineering (Electro-mechanics, Mechanics or Industrial) or equivalent experience in high-technology projects
  • Extensive experience, preferably in the design, procurement, installation and qualification of high-technology or hot cell equipment
  • Experience with driving risk assessments is a strong asset
  • Experience in the nuclear and/or (radio)pharmaceutical industries is essential
  • Knowledge of international standards, such as ISO, ASME, GMP and EHS Regulations
This is a superb opportunity if you are looking for a long-term opportunity in the field with a supportive and innovative company that will put you first.

If this role is of interest, please apply now!
#LI-CB1


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