Computer system validation expertise meets GCP compliance at Alimentiv, supporting reliable technology in a regulated clinical research environment. This is a 12-month limited-term assignment.

As a Computer System Validation Specialist, you will validate GCP-regulated systems and software for Alimentiv. The work covers GxP, 21 CFR Part 11, quality systems, and validation documentation. You will collaborate with IT, Quality Assurance, business stakeholders, and external vendors to support compliant project delivery.

Key Responsibilities:

- Execute validation activities for computerized systems and software
- Develop plans, test scripts, matrices, reports, and release documentation
- Coordinate validation testing and document requirements coverage
- Manage defects, deviations, incidents,



and closure documentation
- Guide change management for validated systems and regulatory updates

Requirements:

- Bachelor's degree or equivalent education and experience
- Three to five years of relevant experience
- Experience validating GCP-regulated systems in regulated industries
- Understanding of validation, documentation, change control, and audit readiness
- Strong communication and cross-functional collaboration skills

Apply computer system validation, GCP compliance, and documentation expertise to support Alimentiv’s regulated technology workplace.

📌 Computer System Validation Specialist (Montreal)
🏢 HMG Careers
📍 Montreal