Alimentiv is a global CRO with a singular focus: advancing therapies for patients with gastrointestinal diseases. GI is our WHY and for more than 30 years that purpose has driven our scientific rigour, operational excellence, and deep therapeutic expertise, including supporting more than 70% of IBD compounds in development.
We operate as a private, profit-with-purpose company, channeling our commercial success back into scientific research, technology, and our people. Looking for a new challenge with real impact, ensuring technology meets the highest quality and compliance standards in a regulated environment? As a Computer System Validation (CSV) Specialist , you will play a key role in validating GCP-regulated systems, partnering with IT, Quality, and business teams to deliver compliant, reliable solutions. You'll lead validation activities from planning through execution, influence system quality and integrity, and help drive continuous compliance with industry regulations and best practices.
GI is our WHY and for more than 30 years that purpose has driven our scientific rigour, operational excellence, and deep therapeutic expertise, including supporting more than 70% of IBD compounds in development.
We operate as a private, profit-with-purpose company, channeling our commercial success back into scientific research, technology, and our people. Looking for a new challenge with real impact, ensuring technology meets the highest quality and compliance standards in a regulated environment? As a Computer System Validation (CSV) Specialist , you will play a key role in validating GCP-regulated systems, partnering with IT, Quality, and business teams to deliver compliant, reliable solutions. You'll lead validation activities from planning through execution, influence system quality and integrity, and help drive continuous compliance with industry regulations and best practices.




Execute validation activities for computerized systems and software in compliance with GxP, 21 CFR Part 11, and applicable regulatory requirements
Develop and maintain validation documentation, including validation plans, test scripts, traceability matrices, summary reports, and release documentation
Partner with IT, Quality Assurance, business stakeholders, and external vendors to define validation strategies and ensure successful project delivery
Coordinate and oversee validation testing activities, ensuring requirements are appropriately tested and documented
Manage defects, deviations, and incidents identified during testing, including triage, resolution tracking, and closure documentation
Train and support project teams on validation procedures, tools, documentation standards, and best practices
Provide ongoing guidance on change management for validated systems and stay current with evolving regulatory requirements and industry standards
Bachelor's degree in Computer Science, Information Technology, Engineering, Software Development, or a related field with 3-5 years of relevant experience , or equivalent combination of education and experience
Experience validating GCP-regulated computerized systems and software, ideally within the pharmaceutical, biotechnology, medical device, or other highly regulated industries
Strong understanding of quality system principles, including validation, documentation, change control, training, and audit readiness




Proven ability to collaborate effectively in cross-functional and matrixed environments, building strong relationships with internal stakeholders, business partners, and external vendors
Excellent written and verbal communication skills, with the ability to clearly document, present, and explain technical and compliance-related information
Experience working within Software Development Lifecycle (SDLC) processes; familiarity with automated testing tools and enterprise validation technologies is considered an asset

Education Reimbursement program for full-time employees
Monthly Cell Phone and Remote Work Allowance (dependent on role eligibility)
One time office setup allowance (can be used to purchase a scanner/printer, extra monitor, office furniture, etc.)
Flexible Summer Hours Program from May – September
Full time employees also become beneficiaries of the Alimentiv Trust after one year of employment, and permanent members after 5 years of employment
country/region annual social events in person; social committee and several other optional initiatives designed to support you in feeling like part of the Alimentiv team!
End‑to‑end GI clinical trial services, from protocol design through submission support
Central medical imaging management and endoscopic reading
Alimentiv is committed to building a diverse, inclusive and respectful workplace. We are an equal opportunity employer and consider all qualified applicants for employment without regard to race, colour, ethnicity, national origin, religion or belief, sex, gender identity or expression, sexual orientation, age, marital or family status, disability, or any other characteristic protected by applicable law.
Accommodations are available upon request for persons with disabilities throughout the recruitment and selection process. Bonus
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📌 Computer Validation Engineer (Montreal)
🏢 Alimentiv
📍 Montreal