* As Documentation and Validation engineer, you areresponsible for the validation of automated control systems according to GMP guidelines.
* You write commissioning and qualification test protocols based on user requirements and functional specifications.
* You execute tests accurately and in compliance with GMP regulations.
* You perform risk assessments and document the outcomes clearly.
* You are the point of contact for internal and external stakeholders regarding validation topics.
* You work closely in a project team, following up on schedules and milestones.
* You have an affinity for machines and automation and an interest in accompanying documentation and testing.
* A Bachelor's orMaster's degree in a relevant technical field.
* At least 2 years of relevant experience within a GMP environment.
* Experience with GAMP5, 21CFRpart 11 and CSV.
* Affinity with computerized systems, such as PLC and SCADA.
* Good analytical & communicationskills.
* Willingness to travel sporadically.
* Fluent in English and good knowledge of French and/or Dutch.
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