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BURGEON IT SERVICES

Computerized System Validation (CSV) with SAP Experience

Toronto, ON, Canada

Contract

Within 25 km of Vaughan · About 22.9 km from the city centre

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Job details

Job type: Contract
Apply by: Nov 18, 2026
Experience: 5 – 10 years of professional experience in the Life Sciences industry working for a consulting services organization and/or industry.
Posted: Oct 19, 2026

Original job description

Role: Computerized System Validation (CSV) with SAP Experience

Location: Any nearest Office in Canada [need to support EST time zone]

Duration: Long Term

Domain (Industry): Life Sciences & Pharma

Mandatory skills

Strong communication and presentation skills

SAP validation experience

Data migration experience

Desired skills

Good stakeholder management skills

We are looking for people who have demonstrated proven success in roles and through abilities in Computerized System Validation/Computerized System Assurance, Risk Management, Test Management and Audits.

Below are the role expectations:

5 – 10 years of professional experience in the Life Sciences industry working for a consulting services organization and/or industry.
Good understanding of key pharmaceutical compliance regulations like 21 CFR Part 11, GxP and GAMP 5.
Experience creating, reviewing, and approving / acknowledging validation deliverables.
Strong knowledge of Software Development Life Cycle (SDLC), testing methodologies, risk-based testing, requirement traceability, defect lifecycle management, and quality assurance processes, with the ability to analyze business and functional requirements and identify quality risks.
Knowledge of risk management process and quality management requirements which assures that IT Projects meet Quality and Regulatory requirements.
Experience with validation of SAP system and data migration projects is mandatory
Thorough Knowledge in compliance and validation concepts. (Change, Deviation, Supplier management)
Knowledge of validation tools and templates used in the pharmaceutical industry. Example: HP ALM, Documentum, Veeva and ServiceNow.

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More about this job

Responsibilities

Create, review, and approve or acknowledge validation deliverables for computerized systems, including SAP validation and data migration projects. Apply risk management, testing, audit, and quality assurance practices to help ensure IT projects meet pharmaceutical quality and regulatory requirements.

Requirements

Requires 5–10 years of Life Sciences industry experience, strong communication and presentation skills, and experience with SAP validation and data migration. Candidates should understand pharmaceutical regulations and standards, validation and quality processes, SDLC, risk-based testing, traceability, and tools such as HP ALM, Documentum, Veeva, and ServiceNow.

Skills

Computerized System Validation
Computerized System Assurance
SAP Validation
Data Migration
Risk Management
Test Management
Audit Management
Pharmaceutical Compliance
21 CFR Part 11
GxP
GAMP 5
Risk-Based Testing
Requirements Traceability
Defect Lifecycle Management
Quality Assurance

Visa sponsorship

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Keywords

Computerized System Validation
Computerized System Assurance
SAP
Data Migration
Life Sciences
Pharmaceutical Manufacturing
21 CFR Part 11
GxP
GAMP 5
Risk-Based Testing
Requirements Traceability
Defect Lifecycle Management
Quality Assurance
Risk Management
Test Management
Audits
Change Management
Deviation Management
Supplier Management
HP ALM
Documentum
Veeva
ServiceNow
Stakeholder Management

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