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.
Organization Overview:
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 38,000 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 individuals who are determined to make life better for people around the world.
Lilly is entering an exciting period of growth and we are committed to delivering innovative medicines to patients around the world. Lilly is investing over $3 Billion to create a new state-of-the-art manufacturing site for Drug Substance, in Lebanon, Indiana. The brand-new facility will utilize a variety of Platforms and have the latest technology for API Manufacturing and Technology. This is an exciting once-in-a-lifetime opportunity to help build and operate a new site. The Lilly Lebanon API Manufacturing site will be built using the latest high-tech equipment, advanced highly integrated and automated manufacturing systems, and have a focus on minimizing the impact to our environment. This is an opportunity you don’t want to miss!
What You’ll Be Doing:
You will be part of MQ (Manufacturing and Quality) IT, an organization that drives manufacturing operational excellence and productivity efforts through utilization of technology. MQ IT strives to enable the making of medicine “with safety first and quality always”.
As MES System Integrator your main function is to Design, Develop, Deliver and Qualify the MES solution for the Lebanon API manufacturing facility. You will also partner with the process automation and operations area and global IT teams to determine innovative ways to develop the MES recipes and implement and support global systems and components related to manufacturing execution.
How You’ll Succeed:
- Ensure site operational readiness from MES and Digital Execution Strategy
- Dynamically adapt road map to site evolution/strategic directions, and new trends/issues.
- Partner cross functionally locally and globally to establish and implement site IT roadmap
- Establish a strong site culture based in Lilly values, expectations, and operational excellence standards.
- Execute the MES strategy for Lebanon.
- Proactively influence the business towards replication & standardization to drive value and implement the appropriate technical solutions.
- Evaluate and translate functional requirements into technical solutions.
- Ensure project and/or validation documentation is maintained during lifecycle & release management.
- Develops/assists in the creation and maintenance of the MES interfaces with other Lilly systems
- Accurately translate business processes into technical terms and vice versa
- Build and maintain awareness and knowledge of regulatory, legal, or quality requirements impacting the quality control laboratory, and ensure that solution requirements comply
- Ensure systems remain in a validated state and manage their lifecycle through releases, recapitalization, and retirement
- Ensure the incident, problem, configuration, and change/release management are all accomplished in alignment with and understanding of business needs
- Partners and builds relationships with cross-functional peers at the manufacturing site and across centralized support organization
- Acts as key contact and subject matter expert for MES IT systems
- Develops training materials
What You Should Bring:
- Deep knowledge and experience with Manufacturing Execution Systems, preferably Emerson’s Syncade platform.
- Understanding of regulatory requirements in GMP (Good Manufacturing Practice), such as FDA regulations for pharmaceutical manufacturing.
- Solid knowledge of Computer System Validation process
- Demonstrated ability to analyze, anticipate, and resolve complex issues (technical, operational, or business-related) through sound problem-solving techniques.
- Effectively prioritize and escalate issues
- Demonstrated learning agility and curiosity
- Demonstrated ability to understand quality control business processes and convert into IT requirements/solutions
- Must have excellent communication skills.
Basic Qualifications:
- Bachelor of Science degree in IT, Chemistry, Pharmacy, Science, Engineering, or related field
- 5+ years of relevant work experience in MES and DCS integration
- Professional experience working in a GXP, regulated environment.
Additional Preferences:
- Deployment, support, management of Syncade MES technologies
- Some knowledge of recipe authoring technologies and techniques
- Previous Agile experience.
- Experience deploying new system implementations
Other Information:
- Role is Monday through Friday and based on-site. Must be flexible in providing support to accommodate other inputs (production schedules, shutdowns, etc.). Occasional extended hour and / or off-hour work may be required.
- Position will be based out of the Lebanon, IN site with ability to travel to other US and global Lilly sites as required.
Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.
Lilly is an EEO/Affirmative Action Employer 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.
Our employee resource groups (ERGs) offer strong support networks for their members and help our company develop talented individuals for future leadership roles. Our current groups include: Africa, Middle East, Central Asia Network, African American Network, Chinese Culture Network, Early Career Professionals, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinos at Lilly, PRIDE (LGBTQ + Allies), Veterans Leadership Network, Women’s Network, Working and Living with Disabilities. Learn more about all of our groups.
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What We Do
Eli Lilly and Company engages in the discovery, development, manufacture, and sale of products in pharmaceutical products business segment.
For more than a century, we have stayed true to a core set of values – excellence, integrity, and respect for people – that guide us in all we do: discovering medicines that meet real needs, improving the understanding and management of disease, and giving back to communities through philanthropy and volunteerism.
