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Validation Specialist - Serialization, Vision & Automated Inspection Systems

  • Québec, QC
  • On-site
  • Posted Oct 10, 2026
  • 1 position

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Employment type
Full-time
Experience level
Mid-level · 2+ years
Minimum education
Professional degree
Posting language
English
Working hours
40 hours per week

Job summary

The Validation Specialist is responsible for creating and maintaining validation documentation such as IQ, OQ, and test protocols for serialization and inspection systems. They also collaborate with internal teams and clients to ensure compliance with regulatory standards and perform risk analyses to support quality improvement.

Job details

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, updating, and maintaining the validation documentation required for OPTEL systems, including internal test protocols, Installation Qualifications (IQ), Operational Qualifications (OQ), and change controls. They help ensure that packaging inspection serialization systems (L1–L2) meet pharmaceutical industry requirements, as well as expected standards of quality, compliance, and reliability. This role requires strong attention to detail in documentation, a solid understanding of regulated environments, and the ability to collaborate effectively with internal teams and clients to support successful project delivery. Tasks: Validation documentation and management: Develop and maintain standardized validation templates for internal use and for clients that comply with industry standards and regulatory guidelines, such as Good Automated Manufacturing Practice (GAMP), FDA 21 CFR Part 11, and EU Annex 11, V-Cycle. Review and interpret 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 and compliance. Risk Analysis and Quality Improvement: Actively participate in risk analyses to identify potential risks associated with validation activities and develop mitigation strategies. Identify root causes following validation non-conformities and implement corrective actions for continuous quality improvement. Collaboration and Expertise: Coordonate 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

What you’ll do

The Validation Specialist is responsible for creating and maintaining validation documentation such as IQ, OQ, and test protocols for serialization and inspection systems. They also collaborate with internal teams and clients to ensure compliance with regulatory standards and perform risk analyses to support quality improvement.

Requirements

Candidates must hold a college diploma in a relevant field and possess at least 2 years of experience in system testing, validation, or technical writing. Proficiency in English, advanced Microsoft Office skills, and a strong aptitude for learning new technologies are required.

Benefits

  • Competitive compensation
  • Flexible working hours
  • Employee Assistance Program
  • Comprehensive group insurance plan

Listed skills

  • Quality assurance · Preferred
  • Microsoft Office · Preferred
  • Attention to detail · Preferred
  • Communication · Preferred

Other relevant skills

Identified from the job description. Confirm important requirements above.

  • Validation documentation
  • System testing
  • Technical writing
  • GAMP
  • FDA 21 CFR Part 11
  • EU Annex 11
  • V-Cycle
  • Risk analysis
  • Quality assurance
  • Microsoft Office
  • Visual Basic
  • VBA
  • Artificial intelligence
  • Analytical skills
  • Attention to detail
  • Communication
  • Good Automated Manufacturing Practices
  • Stakeholder Communications
  • Industry Standards
  • Smart Manufacturing
  • Validation Protocols
  • Compliance Risk
  • Curiosity
  • Willingness To Learn
  • Medical Devices
  • Project Delivery
  • Quality Improvement
  • Analytical Skills
  • Visual Basic (Programming Language)
  • Title 21 Of The Code Of Federal Regulations
  • Artificial Intelligence
  • Management
  • Change Control
  • Continuous Quality Improvement (CQI)
  • Creativity
  • Serialization
  • Design Specifications
  • Employee Assistance Programs
  • English Language
  • Excel Macros
  • External Auditing
  • Packaging And Labeling
  • Hotfix
  • Innovation
  • Internal Auditing
  • Pharmaceuticals
  • Quality Assurance
  • Safety Assurance
  • System Testing
  • Technical Writing

Job areas

  • Technology
  • Manufacturing
  • Healthcare
  • Engineering
  • Validation Specialist
  • Occupational Therapist
  • Health Professionals Not Elsewhere Classified
  • Occupational Therapists

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