Tech@Lilly MES System Engineer

Overview

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At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.

At Lilly in Germany , we are currently planning and building a high-tech production facility in Alzey (Rhineland-Palatinate), which will expand our production of injectable drugs from 2027 and employ up to 1,000 specialists. To make the most of our innovative production site, we are looking for motivated reinforcements who, together with us, will ensure the supply of Lilly medicines in Germany, Europe, and worldwide, in line with the three Lilly values of "Excellence," "Integrity," and "Respect for People."

Responsibilities

• As MES system engineer, your main function is to design, develop, implement, enhance, and maintain the MES software application that help optimize manufacturing processes, reduce errors, and increase efficiency, by integrating production operations with business systems. You will also play a key role as Process Team member to have direct ownership of the day-to-day operations at the manufacturing site representing the function.
• Design, develop, implement, enhance, and maintain our MES solution that integrates production processes with business systems to optimize manufacturing efficiency, quality, and safety.
• Collaborate with cross-functional teams to drive continuous improvement in manufacturing operations.

Key Objectives/Deliverables

• Ensure MES system is in compliance with industry-specific regulations, such as FDA guidelines and GMP requirements, Lilly policy and procedures, and local procedures to maintain product quality and safety.
• Conduct testing, troubleshooting, and ongoing maintenance of MES to ensure system reliability and accuracy of data. Stay up to date with emerging trends in MES technologies.
• Document processes and procedures for all activities to meet quality and compliance standards.
• Strong analytical and problem-solving skills; excellent communication skills; ability to influence the business to drive value and implement digital solutions.

Basic Qualifications

• Bachelor’s degree in software engineering, Computer Science, Computer Engineering, or a related field.
• Minimum of 2+ years’ experience with an MES system (Rockwell Pharma suite preferred), preferably in the pharmaceutical or life sciences industry.
• Excellent communication and interpersonal skills to build relationships with stakeholders and articulate complex technical concepts.
• Strong analytical and problem-solving skills to identify and resolve technical issues related to MES systems, configurations, or integrations.
• Adaptability and flexibility to work in a fast-paced and dynamic environment (Agile mindset).

Additional Skills/Preferences

• Master’s degree in Software Engineering, Computer Science, Computer Engineering, or a related field.
• Experience with MES technologies such as Rockwell Automation Pharma Suite, Emerson Syncade, Siemens Camstar, or Werum PAS-X.
• Programming skills in C++, Java, Python, and SQL; familiarity with ISA-95, OPC, and data historians.
• Experience integrating MES with ERP, EWM, SCADA, and other enterprise systems.
• Understanding of cybersecurity concepts related to MES; knowledge of GMP and FDA regulations; experience with Computer System Validations.
• Experience with agile project management tools (e.g., Jira) and software lifecycle practices.
• Experience mentoring technical team members; exposure to international/global IT projects.
• Proficiency with ServiceNow for incident and change management; HP-ALM and Jira for testing.

This job description is intended to provide a general overview of the job requirements at the time it was prepared. The job requirements of any position may change over time and may include additional responsibilities not specifically described here. Lilly is dedicated to equal opportunity and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status. If you require accommodation to submit a resume, please complete the accommodation request form for further assistance.

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