Join Lilly as a MES System Engineer and be pivotal in transforming our manufacturing operations. You will bridge business needs and technology, ensuring compliance and addressing challenges while working on innovative solutions.
Key Responsibilities
Develop and integrate MES common and site-specific components.
Assist in the creation and maintenance of the MES interfaces with other Lilly systems.
Evaluate and translate functional requirements into technical solutions.
Support MES solutions start-up activities.
Work with site resources towards replication & standardization to drive value.
Ensure project and/or validation documentation is maintained during lifecycle & release management.
Evaluate new technologies and implications to existing Lilly footprint.
Benchmark on innovative solutions.
Maintain open communication with MES vendor(s).
Adapt roadmap to site evolution/strategic directions.
Required Qualifications
Bachelor’s degree in engineering, Computer Science, Information Technology, or a related technical field.
Minimum 2 years of experience working with Manufacturing Execution Systems (MES) in the pharmaceutical or life sciences industry.
2+ years technical ability to develop and integrate MES solutions.
Preferred Qualifications
Pharmaceutical Manufacturing Regulatory compliance knowledge and experience (cGMP)
Experience with MES platforms such as PMX, PharmaSuite, Syncade-DeltaV MES, Werum PAS-X, or similar.
Understanding of GMP regulations and Computer System Validation (CSV) principles.
Benefits & Perks
Company-sponsored 401(k)PensionVacation benefitsMedical, dental, vision and prescription drug benefitsFlexible benefitsLife insurance and death benefitsEmployee assistance programFitness benefitsEmployee clubs and activities