A leading consultancy in life sciences is seeking a Medior Computer System Validation Consultant in Fleurus, Belgium. This full-time role focuses on the validation and documentation of regulated computerized systems in a GMP environment. Responsibilities include performing CSV activities, drafting User Requirement Specifications, and ensuring compliance with regulatory guidelines. The ideal candidate has strong CSV experience, excellent documentation skills, and fluency in both French and English. Join us to make an impact in the pharmaceutical and medical device industries.
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