Validation Specialist - Middleware Solutions

OPTEL is one of the world’s leading providers of traceability systems. Its mission is to leverage innovative technologies to create a better world through responsible capitalism. The company’s renowned solutions ensure the quality of healthcare products and help fight the counterfeiting of medicines and medical devices worldwide. OPTEL also adapts its technologies to a variety of sectors, from healthcare to smart manufacturing and beyond, enabling all industries to benefit from global traceability. OPTEL’s expertise empowers industries to measure, inspect, control, and track a wide range of elements in order to improve product quality and promote a more responsible use of resources. Summary: The Validation Specialist is responsible for creating and maintaining validation documents, such as internal validation protocols, Installation Qualification (IQ), Operational Qualification (OQ), and Change Controls, to ensure that Optel systems comply with industry standards. This role requires expertise in documentation, a drive for innovation through continuous improvement, and the ability to collaborate with internal teams and clients to ensure project validation and quality control. Tasks: Validation documentation and management: Manage the validation template lifecycle: maintain, optimize, and automate existing templates (using MS Office Suite and VBA macros) to increase efficiency while ensuring regulatory compliance, such as Good Automated Manufacturing Practice (GAMP), FDA 21 CFR Part 11, and EU Annex 11. Identify and implement continuous improvement opportunities, including leveraging Artificial Intelligence tools to streamline document drafting and review processes. Review and understand system updates, including new releases and hotfixes, to determine the impact on validation documents. Generate validation documents for clients based on the functional and design specifications of the projects. Execute internal validation protocols as needed to ensure system functionality. Risk Analysis and Quality Improvement: Identify potential risks associated with validation activities and develop mitigation strategies. Lead root cause investigations for validation discrepancies and implement corrective actions for continuous quality improvement. Collaboration and Expertise: Partner with various internal departments to deliver validation documentation at specific stages of project development. Collaborate closely with the internal team and clients to provide expert guidance on validation strategies and best practices. Work closely with the quality assurance (QA) team to ensure that validation activities are in line with internal quality systems and external regulatory requirements by participating in internal and external audits. Perform any other tasks related to validation processes Requisite Skills: College diploma in a relevant field. Minimum of 2 years of experience in system testing and validation or in technical writing. Excellent proficiency in English (written and spoken). Advanced knowledge of the Microsoft Office suite (World). Knowledge of macros (Visual Basic / VBA) in Word and Excel is considered an asset. Strong interest and aptitude for adopting new technologies, including the practical application of Artificial Intelligence for task optimization. Rigor, analytical skills, and attention to detail. Ability to collaborate effectively within a team and communicate with stakeholders at all levels. Strong curiosity and a willingness to learn and adopt new technologies, especially artificial intelligence. Benefits: Competitive compensation Flexible working hours Employee Assistance Program (EAP) Comprehensive group insurance plan A global organization with a presence on several continents OPTEL is an equal opportunity employer. We believe that diversity is essential to fostering innovation and creativity. We welcome and encourage applications from individuals of all backgrounds, cultures, gender identities, sexual orientations, abilities, ages, and beliefs. We are committed to providing a fair and inclusive recruitment process in which every candidate is evaluated solely on their qualifications, skills, and potential. At OPTEL, each employee’s unique perspective contributes to our collective success, and we celebrate the richness that diversity brings to our tea

The Validation Specialist creates and maintains critical validation documents, including IQ, OQ, and change controls, to ensure system compliance with industry standards. They are also responsible for optimizing templates using VBA and AI while collaborating with internal teams and clients to ensure quality control.

Candidates must have a college diploma and at least 2 years of experience in system testing, validation, or technical writing. Proficiency in English and the Microsoft Office suite is required, with VBA knowledge and an aptitude for AI tools considered assets.

• Competitive Compensation • Flexible Working Hours • Employee Assistance Program (EAP) • Comprehensive Group Insurance Plan

Identified from the job description. Confirm important requirements above.

• Validation Documentation
• Installation Qualification (IQ)
• Operational Qualification (OQ)
• Change Control
• GAMP
• FDA 21 CFR Part 11
• EU Annex 11
• VBA Macros
• Risk Analysis
• Root Cause Investigation
• Technical Writing
• System Testing
• Microsoft Office Suite
• Artificial Intelligence Application
• Quality Assurance
• Stakeholder Communication
• Good Automated Manufacturing Practices
• Stakeholder Communications
• Industry Standards
• Smart Manufacturing
• Qualification Protocols (IQ/OQ/PQ)
• Validation Protocols
• Curiosity
• Willingness To Learn
• Medical Devices
• Quality Improvement
• Analytical Skills
• Visual Basic (Programming Language)
• Microsoft Excel
• Title 21 Of The Code Of Federal Regulations
• Artificial Intelligence
• Management
• Regulatory Compliance
• Continuous Improvement Process
• Continuous Quality Improvement (CQI)
• Creativity
• Design Specifications
• Employee Assistance Programs
• English Language
• Excel Macros
• External Auditing
• Hotfix
• Innovation
• Internal Auditing
• Project Management
• Microsoft Office
• Regulatory Requirements
• Safety Assurance
• Visual Basic For Applications
• Product Quality (QA/QC)

• Software
• Engineering
• Manufacturing
• Healthcare
• Technology
• Middleware Specialist
• Validation Specialist
• Process Control Technicians Not Elsewhere Classified
• Validation Engineers
• Industrial Engineers

Minimum education

College diploma

Minimum experience

2+ years

Apply by

Oct 18, 2026

Posting language

English

Working hours

40 hours per week