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
Solid detail orientation and analytical skills
Team-oriented mindset for internal and external communication Support OPTEL’s vision for responsible capitalism while enhancing product quality across healthcare and beyond.

📌 Optel Validation Specialist For Quality Assurance Quebec City (Canada)
🏢 Optel Vision
📍 Canada