Elevate product quality in healthcare as a Validation Specialist with OPTEL in Canada. Focus on creating regulatory-compliant documentation and innovating internal processes. As a Middleware Validation Specialist, you will manage validation documentation, ensuring compliance with industry standards.

Key skills include system testing, collaboration with internal teams, and continuous improvement using AI tools. Your creative approach will significantly impact how we maintain and assure the quality of vital healthcare technologies. Key Responsibilities:
Manage validation template lifecycle for regulatory compliance
Utilize AI tools for productive document drafting
Generate and review validation documents for client specifications
Identify risks in validation processes and develop strategies
Collaborate with teams to ensure quality assurance compliance Requirements:
College diploma in a relevant field
2+ years in system testing or validation
Proficiency in Microsoft Office and VBA
Solid analytical skills and attention to detail
Effective communication with stakeholders Drive continuous improvement and quality assurance as part of OPTEL’s cutting-edge team.

📌 Middleware Validation Specialist At Optel Quebec City (Canada)
🏢 Optel Vision
📍 Canada