Senior SAP Validation Consultant With IT CSV Experience
- Toronto, Ontario, Canada
- Remote
- Posted Oct 17, 2026
- 1 position
Opens LinkedIn
- Employment type
- Contract
- Experience level
- Senior · 5+ years
- Posting language
- English
- Working hours
- 40 hours per week
- Location requirements
- Country, Toronto, Ontario, Canada
- Seniority
- Mid-Senior level
- Application method
- Apply on LinkedIn (LinkedIn sign-in required)
Job summary
Create, review, and approve or acknowledge validation deliverables for SAP validation and data migration projects. Apply risk management, test management, quality assurance, and regulatory compliance practices, and support audits and validation processes.
Job details
Position: Senior SAP Validation Consultant with IT CSV Experience Location: Remote Duration: Long Term Contract Mandatory skills* Strong communication and presentation skills SAP validation experience Data migration experience Domain (Industry)* Life Sciences & Pharma 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.
What you’ll do
Create, review, and approve or acknowledge validation deliverables for SAP validation and data migration projects. Apply risk management, test management, quality assurance, and regulatory compliance practices, and support audits and validation processes.
Requirements
Requires 5–10 years of Life Sciences industry experience and demonstrated experience with SAP validation and data migration projects. Candidates should understand 21 CFR Part 11, GxP, GAMP 5, SDLC, risk-based testing, traceability, quality management, and pharmaceutical validation tools.
Listed skills
- Change Management · Preferred
- Quality assurance · Preferred
- Risk Management · Preferred
Other relevant skills
Identified from the job description. Confirm important requirements above.
- SAP Validation
- Computerized System Validation
- Computerized System Assurance
- Data Migration
- Risk Management
- Test Management
- Audit Management
- Pharmaceutical Compliance
- Validation Deliverables
- Software Development Life Cycle
- Risk-Based Testing
- Requirements Traceability
- Defect Lifecycle Management
- Quality Assurance
- Change Management
- Deviation Management
Job areas
- Technology
- Consulting
- Healthcare
- Security & Safety
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