About the role

SAP Senior Functional Consultant ensuring SAP integrations and optimizations within Manufacturing and Quality modules. Driving impactful projects and collaborating with cross-functional teams at Evotec.

Responsibilities

Lead the design, implementation, and support of SAP Manufacturing (PP-PI) and Quality (QM) processes, ensuring robust system configurations and continuous improvements.
Architect and drive initiatives to integrate SAP with PAS-XMES systems to automate data exchange from production execution.
Oversee connectivity and data flow between SAP and Labware, ensuring streamlined quality management and laboratory information transparency.
Serve as a subject matter expert and strategic advisor by gathering business requirements and translating them into SAP and system integration solutions.
Collaborate closely with IT, supply chain, operations, production equipment engineers, and quality assurance teams to drive cross-functional process enhancements.
Manage SAP system upgrades, patches, and continuous improvement projects while ensuring timely issue resolution to minimize operational disruptions.
Develop detailed documentation, including functional specifications, integration architecture diagrams, process flow charts, and training materials.
Provide end-user training on new integrations and system enhancements, ensuring smooth adoption and high levels of operational proficiency.
Ensure all processes adhere to industry standards, GxP regulations, FDA 21 CFR Part 11, and internal governance frameworks.
Monitor system performance and integration functionalities to support audit readiness and risk mitigation.

Hands-on SAP functional consulting experience with a strong track record in Manufacturing (PP-PI) and Quality (QM) modules.
Proven expertise in integrating SAP with MES platforms (e.g., PAS‑X or equivalent) and LIMS solutions (e.g., LabWare or comparable systems), ensuring seamless interoperability across production and laboratory environments.
Deep expertise in SAP S/4HANA configuration, testing, troubleshooting, and continuous improvement initiatives.
Strong analytical and problem-solving capabilities, with a demonstrated ability to translate complex business requirements into efficient, integrated SAP solutions.
Experience working within pharmaceutical, biotech, or similarly regulated manufacturing environments.
Familiarity with GxP protocols, FDA regulatory compliance, ISO standards, and other pertinent quality assurance standards.
Bachelor’s degree in Information Technology, Engineering, Business, or a related field.
SAP certifications in PP, QM, or S/4HANA are highly desirable.
Additional credentials or training in MES (e.g., PAS‑X) and LIMS (e.g., LabWare) integration will be considered a significant asset.
Proficiency in French would be highly desirable
Proven ability to work independently while fostering a collaborative team environment across multiple disciplines.