Lead, Computerized Systems Validation - Canada

Argentina
Remote
Posted Oct 26, 2026
1 position

Opens an external site

Employment type: Full-time
Experience level: Lead · 10+ years
Posting language: English
Working hours: 40 hours per week

Job summary

Lead complex, high-risk validation initiatives across the lifecycle of GxP computerized systems, including strategy, risk assessment, documentation, execution, and release or retirement. Provide technical oversight, coordinate project schedules and stakeholders, mentor analysts, and support audits, inspections, and continuous improvement of CSV practices.

Job details

The CSV Lead is a senior individual contributor and subject matter expert responsible for leading complex, high-risk computerized system validation initiatives across the system lifecycle. Working in close collaboration with the Associate Director, Computerized Systems Validation, the CSV Lead provides technical expertise for validation strategy, planning, execution, and reporting; ensures the quality and completeness of validation deliverables; and promotes consistent application of risk-based, data-integrity, and GxP requirements. The role partners with system owners, operations, IT, Quality, and vendors. The position does not carry routine people-management accountability but may coordinate project teams and provide functional direction. Requirements More specifically, the CSV Lead: Leads validation workstreams for new GxP computerized systems, upgrades, and system retirements, coordinating activities and deliverables with system owners, business functions, IT, Quality, and vendors. Facilitates project initiation and risk-assessment discussions to determine GxP impact, system criticality, validation scope, applicable controls, supplier leverage, and the risk-based validation strategy. Develops, reviews, and/or approves by applicable procedures, validation deliverables including validation plans, user requirements specifications, system risk assessments, functional and configuration specifications, test scripts, data migration verification, traceability matrices, deviation records, and validation summary reports. Provides technical oversight of validation execution, ensures objective evidence is complete and attributable, and drives the timely resolution of test defects, discrepancies, and documentation gaps before release or closure. Performs peer reviews of validation packages and takes accountability for ensuring assigned packages are complete, internally consistent, traceable, inspection-ready, and compliant with applicable policies, SOPs, regulations, and industry practices. Assesses vendor validation documentation to determine the extent to which supplier evidence may be leveraged and supports vendor qualification or audit activities when required. Leads or provides CSV oversight for lifecycle controls, including change control, periodic review, access and security considerations, backup and restoration, data migration, archival, business continuity, CAPA, and system retirement. Acts as team support for complex validation or validation strategy, data integrity, electronic records and signatures, cloud/SaaS, interfaces, emerging technology, and other computerized-system issues. Builds effective relationships with system owners and system administrators and provides guidance on their responsibilities for maintaining the validated state of GxP computerized systems. Coordinates project-level CSV schedules, dependencies, priorities, risks, and status reporting; identifies resource or timeline constraints and escalates material risks to the Manager, CSV in a timely manner. Mentors CSV Analysts and provide day-to-day technical direction and review feedback, shares current industry practices, and supports consistent execution across the CSV team. Develops and delivers CSV training for project teams (system owners, business SMEs, testers) as required by projects or process changes. Contribute to the creation and revision of CSV policies, SOPs, templates, tools, metrics, and process-improvement initiatives, and supports implementation of approved changes. Maintains current knowledge of applicable computerized-system regulations, guidance, industry standards, and evolving technologies, including cloud services, connected devices, automation, and artificial intelligence, and recommends appropriate updates to CSV practices. Supports internal audits, vendor audits, client audits and requests for information, and regulatory inspections by preparing evidence, responding to questions, and supporting remediation activities. Our company At Indero, formely Innovaderm, you will work with brilliant and driven colleagues. Our values are collaboration, innovation, reliability and responsiveness. We offer a stimulating work environment and attractive advancement opportunities. As a CSV Lead, you will be eligible for the following perks: Permanent full-time position Flexible schedule Home-based position Ongoing learning and development Work location The successful candidate for this position is given to work remotely on the Eastern part of North America. About Indero, formely Innovaderm Indero, formely Innovaderm is a contract research organization (CRO) specialized in dermatology. Since its beginnings in 2000, our organization has benefited from a solid reputation for the quality of its research and services exceeding the expectations of its clients. Based in Montreal, Indero, formely Innovaderm continues to grow and expand in North America and Europe. Indero, formely Innovaderm is committed to providing equitable treatment and equal opportunity to all individuals. As such, Indero, formely Innovaderm will provide accommodations throughout the recruitment and selection process to applicants with disabilities, upon request. Indero, formely Innovaderm only accepts applicants who can legally work in Canada Description de poste null Profil recherché null Notre entreprise null

What you’ll do

Requirements

The role calls for senior-level expertise in computerized systems validation, GxP requirements, risk-based approaches, data integrity, and validation lifecycle controls. It also requires the ability to coordinate cross-functional projects, review inspection-ready documentation, guide system owners and analysts, and support audits and regulatory inspections.