Join OPTEL in Canada as a Validation Specialist, focusing on middleware solutions and quality assurance documentation. Enhance compliance efforts and innovation through team-oriented practices.

This full-time role demands expertise in maintaining validation documents, including Installation and Operational Qualifications. The ideal candidate will possess a strong analytical mindset and demonstrated success in system validation or technical documentation, contributing to the continuous improvement of quality assurance processes.

Key Responsibilities:
• Manage and optimize validation templates for efficiency
• Generate client-specific validation documentation
• Identify validation process risks and mitigation strategies




• Lead investigations into validation discrepancies
• Collaborate with internal departments on documentation needs

Requirements:
• College diploma relevant to the role
• Minimum 2 years of experience in validation or technical writing
• Proficient in Microsoft Office and VBA
• Strong detail orientation and analytical skills
• Collaborative mindset for internal and external communication

Support OPTEL’s vision for responsible capitalism while enhancing product quality across healthcare and beyond.
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📌 OPTEL Validation Specialist for Quality Assurance (Quebec City)
🏢 Optel Vision
📍 Quebec City