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 settings.
J-18808-Ljbffr
📌 Validation Specialist: Serialization & Automated Inspection Systems Quebec City (Canada)
🏢 OPTEL Group
📍 Canada
Reply to this offer
Impress this employer describing Your skills and abilities, fill out the form below and leave Your personal touch in the presentation letter.