GMP CQV Engineer: Validation, Startups & Compliance
Arcadis
Arcadis is seeking a Validation Engineer to support commissioning, qualification, validation, requalification, and lifecycle management activities within a GMP-regulated pharmaceutical environment. You will develop and execute validation documentation and support capital projects, ensuring compliance with regulatory requirements. The role requires coordinating cross-functional teams across Manufacturing, Facilities, QA, and Engineering, authoring IQ/OQ/PQ, FAT/SAT, and maintaining validated #J-18808-Ljbffr Arcadis
Vacancy posted more than 2 months ago
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