ERP Specialist

LivaNova • Houston, TX

16h • $115,000 - $125,000 • Onsite

About The Position

The ERP Specialist supports and optimizes SAP-driven manufacturing, quality, procurement, and logistics processes across LivaNova’s North America organization. The role provides functional expertise in SAP S/4HANA, with a focus on MM, PP, QM, and IM/WM, to promote operational efficiency, system reliability, and regulatory compliance. The specialist partners with business stakeholders, SAP functional and technical teams, and business process owners to improve critical operations and support business-critical systems in a regulated medical technology environment. This is an on-site position based in Clear Lake, Houston, Texas, with occasional travel of up to 10%.

Requirements

• Bachelor’s degree in Science, Information Technology, Business, or a related discipline.
• At least 10 years of experience with SAP S/4HANA, particularly in manufacturing, warehousing, and procurement environments.
• Experience supporting SAP MM, PP, QM, and IM modules, including multiple full life-cycle implementations.
• Experience supporting SAP users and software validation activities in FDA-regulated environments, following GMP/GxP-compliant processes.
• Strong analytical, problem-solving, technical writing, communication, and presentation skills.
• Ability to manage multiple priorities and independently support multiple sites.

Nice To Haves

• Experience in discrete manufacturing environments, particularly within the life sciences or medical device industries.

Responsibilities

• Analyze, design, configure, test, deploy, and support SAP solutions across MM, PP, QM, and IM/WM, including integrations with other business systems.
• Gather requirements with business stakeholders, develop solution documentation, and identify opportunities to optimize manufacturing, quality, and logistics processes.
• Collaborate with SAP functional and technical teams on system enhancements, WRICEF developments, cross-functional projects, and continuous improvement initiatives.
• Troubleshoot system issues, resolve support tickets, and provide end-user guidance and training while ensuring compliance with FDA and GMP/GxP requirements.
• Prepare and maintain functional specifications, standard operating procedures, test scripts, validation documentation, and training materials.
• Support integrations with manufacturing execution systems (MES), labeling software, and other connected applications.
• Participate in system testing, software validation, implementations, and upgrades while promoting SAP best practices and process efficiency.

Benefits

• Discretionary annual bonus.
• Professional growth and development in an innovative medical technology environment.
• Opportunities to collaborate with international partners and cross-functional teams.
• Competitive compensation.

What This Job Offers

• Job Type: Full-time
• Career Level: Senior