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 in Québec employer: Optel Group
OPTEL is an exceptional employer that champions innovation and responsible capitalism, making a meaningful impact across various industries, including healthcare. With a commitment to employee growth, flexible working hours, and a comprehensive benefits package, OPTEL fosters a collaborative and inclusive work culture where diverse perspectives are valued. As a Project Manager, you will play a crucial role in delivering quality solutions while enjoying the support of a global organization dedicated to your professional development.
