Jobs in Vaughan

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Within 25 km of Vaughan

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SAP Validation SME- IT CSV
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BURGEON IT SERVICES

SAP Validation SME- IT CSV

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

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 SAP systems 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 knowledge of pharmaceutical regulations and validation concepts, and mandatory experience validating SAP systems and data migration projects. Candidates should understand SDLC, testing and risk management processes, quality requirements, and industry tools such as HP ALM, Documentum, Veeva, and ServiceNow.

Skills

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

Visa sponsorship

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Keywords

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

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