SAP QM Consultant

SAP QM Consultant

SAP QM Consultant

Market Cloud

2 hours ago

No application

About

  • **
  • Job role: SAP QM Consultant with Pharma**
  • Experience: 8 yrs and above
  • Location: UK
  • Onsite : Work from Office
  • 🧪 Role Summary
  • An SAP QM Consultant specializing in the pharmaceutical sector designs, configures, implements, and validates the SAP QM module tailored to GMP/GxP-regulated environments. The consultant ensures quality processes—from inspection planning through batch release—are integrated into S/4HANA, supporting compliance and operational excellence
  • Tasks
  • Pharma‑Specific Responsibilities
  • Ensure GxP/GMP compliance throughout SAP QM processes.
  • Translate pharma quality processes (inspection, CAPA, deviation, stability, COA) into SAP QM workflows.
  • Enable integrations with LIMS, MES, and DMS systems, supporting regulatory alignment.
  • Skills & Competencies
  • Deep knowledge of pharma quality processes: inspection planning, deviation, CAPA, stability, COA, batch release.
  • Proficient in documentation: business requirements, functional specs, test scripts, SOPs.
  • Excellent stakeholder management, workshop facilitation, and communication skills.
  • Strong analytical, problem-solving, and process improvement mindset.
  • Ability to guide validation activities, ensure audit-readiness, and support compliance.
  • Coaching and training capabilities for end-users.
  • Requirements
  • Key Responsibilities
  • Lead the design, configuration, and implementation of SAP QM aligned with pharmaceutical industry standards and regulatory compliance.
  • Configure QM master data: inspection types, sampling procedures, quality notifications.
  • Facilitate workshops with stakeholders to capture requirements and translate them into functional specs.
  • Integrate SAP QM with modules like MM, PP, WM, EWM, and compliance systems (LIMS, MES, DMS via BTP/CPI where relevant).
  • Define inspection planning, in-process controls, batch release, deviation/CAPA handling, and stability/COA processes.
  • Support validation and documentation (CSV, IQ/OQ/PQ, test scripts, SOPs, audit trail, e-signatures).
  • Participate in integration testing, UAT, cutover, hypercare, and offer post-go-live support.
  • Identify process improvements and recommend SAP QM best practices for pharma.
  • Develop and deliver training materials; support audits and compliance checks.