About the job Validation engineer aseptic manufacturing
Role and responsabilities:
* Commissioning and qualification of new and existing equipment
* Assuring appropriate risk management in the validation strategy
* Writing URS of pharma equipment
* Performing testing and validation activities (FAT and SAT)
* Ensuring that adequate documentation is available for operations and QA
* You will be working in cross-functional teams in a project or operational environment
Your background:
* Experience in the pharmaceutical sector as validation or C&Q engineer
* Experience in commissioning and qualification of equipment or processes such as formulation, filling, cleaning, sterilization
* Candidate must speak fluent English. Italian is an asset. Dutch is not required.
* The location of the project is NORTHERN ITALY with a good airplane connection to Brussels
Conditions:
Full-time contract. (Freelance also possible)
You will be part of a growing Belgian SME where initiative and personal development are encouraged. We will provide you with an enjoyable work environment with fun colleagues. Well work out a career plan with you, with attention and a budget for extra education/certification. You can count on an attractive salary, supplemented with extra-legal benefits, including a company car.
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