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Trevalco BV is seeking a Validation Consultant to work with clients in the pharmaceutical industry across various validation projects. Responsibilities include developing validation strategies, writing validation plans, and managing quality records. Candidates should be fluent in English and Dutch, possess strong analytical and communication skills, and hold a Master’s degree in science or engineering.
Enjoy a competitive salary, training opportunities, and a healthy work/life balance. Join a Belgian SME and make an impact!
A job as validation consultant in the pharmaceutical industry has a lot of variation. It includes technical analysis, document writing, execution of tests in production or laboratory environments, as well as a lot of interaction with different departments in the company where you work.
As validation consultant you execute validation projects on location at clients in the pharmaceutical industry.
This can be production equipment validation, lab equipment validation but it can also concern the validation of facilities and utilities, processes and computer systems. Depending on your background and interests you will be active in one or more of these areas.
For this position we are looking at all levels of experience, from starter to senior level.
Your responsibilities as validation consultant include:
As an employer, we contribute to the success of your career. Proper guidance and training are very important to us. Naturally, we also ensure that you feel good in your job through a healthy work/life balance, a market-competitive salary, and tailored solutions for aspects such as mobility.
CAO90 bonus, hospitalisation and dental care insurance, meal vouchers and more
you choose what works best: company car or mobility budget
coaching, classroom or digital online training, what works for you
because we have families, friends and hobbies