SAP Data Migration & Validation Consultant - Life Sciences

Infosys Limited

Toronto

Hybrid

CAD 93,000 - 123,000

Full time

8 days ago

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Job summary

Infosys Consulting in Canada (Ontario) seeks an experienced SAP CSV & Data Migration consultant to support ERP transformations and large SAP implementations, with a focus on CSV, data migration controls, and audit readiness. You will collaborate with Quality, Compliance, Validation, Business, and IT teams across modules such as FI/CO, SCM, QM, and MDG.

The role requires 3+ years in Life Sciences consulting, strong regulatory knowledge (21 CFR Part 11, GxP, GAMP 5), and proficiency in validation

Qualifications

  • Minimum 3+ years of Life Sciences consulting or pharma industry experience.
  • Experience creating, reviewing, and approving validation and compliance deliverables.
  • Strong understanding of quality management systems and risk management processes.
  • Familiarity with 21 CFR Part 11, GxP, GAMP 5, Data Integrity, Data Privacy, Information Security, and SOX IT controls.

Responsibilities

  • Lead compliance and validation activities for SAP ECC to SAP S/4HANA transformation and SAP implementations.
  • Oversee ERP testing activities including test planning, script reviews, execution governance, defects, and traceability.
  • Ensure regulatory compliance and audit readiness across projects.
  • Develop and maintain validation artifacts: Validation Plans, Risk Assessments, Traceability Matrices, VRs, Test Protocols.
  • Review Data Migration deliverables: DCMP/R, DMWs, DORs, DMLs, DVTs, reports.

Skills

Compliance
Validation
Quality concepts
ERP test management
Data migration
Audit readiness
SAP testing governance
S/4HANA knowledge
Agile / Waterfall
Stakeholder management

Tools

HP ALM
SAP Solution Manager
SAP CHARM
JIRA
ServiceNow
SNP
ADM
Migration Cockpit

Job description

Infosys Consulting in Canada (Ontario) seeks an experienced SAP CSV & Data Migration consultant to support ERP transformations and large SAP implementations, with a focus on CSV, data migration controls, and audit readiness. You will collaborate with Quality, Compliance, Validation, Business, and IT teams across modules such as FI/CO, SCM, QM, and MDG.

The role requires 3+ years in Life Sciences consulting, strong regulatory knowledge (21 CFR Part 11, GxP, GAMP 5), and proficiency in validation

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