Pharmaceutical Manufacturing Regulatory compliance knowledge and experience (cGMP)
Effective people and team leadership skills
Ability to manage and contribute to multiple concurrent activities and adapt to changes in priorities.
Ability to cross functionally collaborate.
Excellent written and oral communication skills.
Demonstrate creativity, analytical thinking, and the ability to troubleshoot and solve problems.
Knowledge of cloud solutions and architecture
History of promoting safety and maintaining a safe work environment
Establish a strong site culture based in Lilly values, expectations, and operational excellence standards.
Demonstrated adhere adherence to compliance for internal and external quality guidance.
Demonstrated and promote Operational Excellence
Effectively encourage knowledge sharing and education
Evaluate and translate functional requirements into technical solutions.
Ability to problem solving and work through manufacturing situations. Have experience serving as an escalation contact with vendor(s)
Proven technical ability to develop and integrate MES solutions
What Your Primary Responsibilities Will Be:
Develop and integrate MES common and site-specific components.
Benchmark on innovative solutions (external and internal to Lilly)
Dynamically adapt road map to site evolution/strategic directions, and new trends/issues.
Establish a strong site culture based in Lilly values, expectations, and operational excellence standards.
Support MES solutions start up activities.
Work with site resources towards replication & standardization to drive value and implement the appropriate technical solutions.
Evaluate emerging technologies and implications to existing Lilly footprint.
Maintain open communication with MES vendor(s) to address needs in standard solution or via functional packs.
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.
Your Basic Qualifications (with no sponsorship)
Bachelor's Degree in IT, Engineering, or related technical field,
10+ years of strong experience with MES system implementations and Data Integration preferably Syncade/Delta V MES
Professional experience working in a GXP, regulated environment
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.
Benefits
Health insuranceFlexible schedule
Additional Information
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.
Sr Principal Engineer - MES Systems
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 35,000 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 people who are determined to make life better for people around the world.
This is an opportunity you don't want to miss!
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 $50 Billion to create new Manufacturing Capacity throughout the world. This is an exciting once-in-a-lifetime opportunity to help build and start up new sites.