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.What You’ll Be Doing:You will be part of Tech at Lilly MQ (Manufacturing and Quality), an organization that drives manufacturing operational excellence and productivity efforts through utilization of technology. Tech at Lilly MQ strives to enable the making of medicine “with safety first and quality always”.As a MES system engineer within the IT organization that supports the Alcobendas packaging site, you will play a critical role in designing and supporting and develop Manufacturing Execution System (MES) electronic batch records and logbook, associated tools, and system interfaces to fulfil business needs. Deploys existing systems, analyses information, designs, programs and/or implements new systems or enhancements to existing systems in accordance with company standards and guidelines.How You’ll Succeed:- Work within a team to analyze business processes and needs to recommend or implement changes to systems and/or procedures.- Work closely with internal teams (IT, manufacturing, quality, technical services) to gather requirements, create designs, and deliver MES solutions that enhance operational efficiency.- Understand how the manufacturing execution systems and processes integrate with other critical systems like EWM (Extended Warehouse Management).- Continuously evaluate and implement new technologies and methodologies to enhance system functionality, data flow, and overall operational efficiency.- Provide technical leadership, guidance, and mentorship to cross-functional teams on MES system design.- Provides training, documentation, and post-implementation support to users of the new application and or systems.- Coordinates or performs technical testing and installation with appropriate users and systems personnel. Prepares project justification, scope and timeline and ensures project complies with these commitments.- Ensure that all solutions adhere to regulatory, compliance, and security standards, including GxP, ensuring data and system integrity.- Participates and/or represents departments in cross-functional, global and/or departmental teams and forums as requested.What You Should Bring:- Strong experience designing and implementing IT and data architectures in a highly regulated, manufacturing or pharmaceutical environment, including systems like MES (e.G., Pharmasuite, Syncade, Werum PAS-X) and ERP (e.G., SAP).- Strong analytical and problem-solving skills.- Excellent collaboration and communication skills to work with cross-functional teams, leadership, and global teams effectively.- Experience as an autonomous IT leader leading medium-size portfolios and high demanding customers.- Demonstrated ability to influence IT and business strategies to drive medium-size outcomes.- Validated skills of strong learning agility and relationship building to influence change using knowledge and relationships.- Successful record of high quality, user focused, on-time & budget IT service and project delivery.- Experience with formal project management methodologies, agile frameworks and working knowledge of associated practices and tools.- A high level of intellectual curiosity, external perspective, and innovation interest.Basic Requirements:- Bachelor’s Degree in Computer Science, Information Technology or related technical field- C1/ Advanced in English- 4 - 10 years' experience in IT and/or Engineering Automation/control systems-related fields.- 3+ years' experience with design, development, testing, delivery, and support of Electronic Batch Record(s) using Rockwell PharmaSuite or similar MES- Strong knowledge of GxP, FDA, and other regulatory requirements.- Ability to work in a fast-paced, global, and regulated environment, with a focus on operational excellence.Additional Preferences:- Master’s degree in Computer Science, Information Technology, Business Administration, or a related field is preferred.#J-18808-Ljbffr