Join OPTEL in Canada as a Validation Specialist, focusing on middleware solutions and quality assurance documentation. Enhance compliance efforts and innovation through collaborative 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
- Collaborative 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)
🏢 Optel Vision
📍 Quebec City