SAP Senior Functional Consultant – Manufacturing (PP-PI), Quality (QM) - Hybrid Seattle, WA or open to Remote Working

Just-Evotec Biologics • Seattle, WA

26d • $134,000 - $154,000 • Hybrid

About The Position

We’re looking for a passionate and curious SAP Senior Functional Consultant – Manufacturing (PP-PI), Quality (QM) to join our team. If you’re excited by new challenges, solving complex problems, and learning every step of the way, you might just be the perfect fit. In this role, you’ll have the opportunity to drive impactful projects, collaborate with bright minds, and explore uncharted territories. As our SAP Senior Functional Consultant, you will lead design, implementation, and system enhancement initiatives within the Manufacturing (PP-PI) and Quality (QM) modules. Your role will be pivotal in optimizing SAP solutions and ensuring smooth integration with key operational systems, specifically MES platforms PAS‑X and LIMS systems LabWare. By bridging these domain technologies, you will enable end-to-end process automation, data integrity, and compliance within our highly regulated environment. As our SAP Senior Functional Consultant – Manufacturing (PP-PI), Quality (QM) at Evotec , you'll have the freedom to ask the hard questions, think outside the box, and find creative solutions that push us forward. It’s a role where your curiosity will fuel both your personal growth and the success of the team.

Requirements

• 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.
• Proven ability to work independently while fostering a collaborative team environment across multiple disciplines.

Nice To Haves

• 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.

Responsibilities

• SAP Process Leadership and Design End-to-End SAP Solutions: Lead the design, implementation, and support of SAP Manufacturing (PP-PI) and Quality (QM) processes, ensuring robust system configurations and continuous improvements.
• Integration: 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.
• Stakeholder Collaboration and Leadership 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.
• System Enhancements and Troubleshooting 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.
• Training and Support Provide end-user training on new integrations and system enhancements, ensuring smooth adoption and high levels of operational proficiency.
• Work in partnership with our AMS Partner to implement and troubleshoot end-to-end solutions, supporting a robust and scalable environment.
• Compliance and Regulatory Adherence 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.

Benefits

• Growth Opportunities
• Flexible Work Environment
• Inclusive Culture
• Innovative Projects
• A Place for Big Ideas
• discretionary annual bonus
• comprehensive benefits to include Medical, Dental and Vision, short-term and long-term disability, company paid basic life insurance, 401k company match, flexible work, generous paid time off and paid holiday, wellness, and transportation benefits

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Number of Employees: 1,001-5,000 employees