12 Oct
|
OPTEL Group
|
Quebec City
12 Oct
OPTEL Group
Quebec City
OPTEL is seeking a Validation Specialist to create, update, and maintain validation documentation for packaging inspection serialization systems, including IQ, OQ, and change controls. The role ensures compliance with GMP, FDA 21 CFR Part 11, and EU Annex 11 while delivering high-quality documentation for projects.
You will collaborate with internal teams and clients, analyze risks, drive quality improvements, and support successful project delivery in regulated environments.
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📌 Validation Specialist: Serialization & Automated Inspection Systems (Quebec City)
🏢 OPTEL Group
📍 Quebec City