Sr Principal Engineer - Mes Systems

Eli Lilly Eli Lilly · Pharma · Richmond, VA

This role is for a Sr. Principal Engineer focused on Manufacturing Execution Systems (MES) within a pharmaceutical manufacturing facility. The primary responsibilities involve developing and integrating MES components, supporting site startups, and ensuring compliance with cGMP regulations. The role requires extensive experience with MES systems and data integration in a regulated environment.

What you'd actually do

  1. Develop and integrate MES common and site-specific components.
  2. Benchmark on innovative solutions (external and internal to Lilly)
  3. Dynamically adapt road map to site evolution/strategic directions, and new trends/issues.
  4. Establish a strong site culture based in Lilly values, expectations, and operational excellence standards.
  5. Support MES solutions start up activities.

Skills

Required

  • 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

Nice to have

  • 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)

What the JD emphasized

  • Pharmaceutical Manufacturing Regulatory compliance knowledge and experience (cGMP)
  • Proven technical ability to develop and integrate MES solutions
  • 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