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 solid 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 (Winnipeg)
🏢 Optel Vision
📍 Winnipeg