Become an integral part of OPTEL’s mission to enhance traceability systems as a Validation Specialist specializing in middleware solutions. Engage in innovative documentation practices and quality assurance.

In this full time position, you will produce and manage validation documents ensuring they meet core industry regulations, such as GAMP and FDA guidelines. Effective collaboration with diverse teams and a focus on cutting-edge technologies are crucial for this role, which aims for iterative improvement in validation processes.

Key Responsibilities:
• Oversee lifecycle of validation documentation templates
• Implement AI solutions for document optimization
• Review system updates impacting validation requirements
• Conduct root cause analysis on validation issues
• Partner with QA teams for compliance audits

Requirements:
• Relevant college diploma required
• 2+ years in technical writing or validation
• Advanced MS Office and VBA skills
• Detail-oriented with strong analytical abilities
• Curiosity for emerging technologies and learning

Transform validation practices at OPTEL while promoting superior healthcare quality.
#J-18808-Ljbffr

📌 Validation Specialist with AI Focus at OPTEL (Quebec City)
🏢 Optel Vision
📍 Quebec City