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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 processesfrom inspection planning through batch releaseare integrated into S/4HANA supporting compliance and operational excellence
Tasks
PharmaSpecific 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.
**Job role: SAP QM Consultant with Pharma**Experience: 8 yrs and aboveLocation: UKOnsite : Work from Office Role SummaryAn SAP QM Consultant specializing in the pharmaceutical sector designs configures implements and validates the SAP QM module tailored to GMP/GxP-regulated environments. The consult...
**
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 processesfrom inspection planning through batch releaseare integrated into S/4HANA supporting compliance and operational excellence
Tasks
PharmaSpecific 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.
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