DeltaV MES Engineer – Regulated Pharma, Onsite Houston

BioSpace; Houston (TX); On-site; USD 66,000 - 158,000; Full time

Job summary

Lilly is pursuing a MES Engineer to join the API Manufacturing Site in Houston, Texas. The role supports design, development, delivery, and validation of the DeltaV MES solution to meet site operational, quality, and compliance needs.

You will work with Operations, Quality, Engineering and IT to ensure successful deployment and ongoing support. Ideal candidates have 5+ years in MES, experience with DeltaV/Syn Cade, and familiarity with regulatory requirements (cGMP).

Qualifications

• Bachelor’s degree in IT, Engineering, or related technical field is required.
• 5+ years of MES design, implementation, and validation experience.
• 3+ years in regulated pharmaceutical or medical device manufacturing environments.
• Authorized to work in the United States full-time (visa sponsorship not provided).
• Experience with DeltaV/Syn Cade and MES interfaces to ERP/Historian/DCS is preferred.

Responsibilities

• Partner with site teams to gather requirements and define digital workflows.
• Configure MES recipes, workflows, and electronic batch records (EBRs).
• Configure electronic logbooks, Weigh & Dispense, and MES interfaces with other systems.
• Assist with site readiness, testing, and validation (IQ, PQ) and CSV documentation.
• Troubleshoot MES issues and collaborate across multidisciplinary teams.
• Produce and maintain system documentation, SOPs, and training materials.

Skills

Analytical thinking

Communication skills

Cross-functional collaboration

Regulatory knowledge (cGMP)

No-code/low-code experience

Education

Bachelor’s degree in IT/Engineering or related

Tools

DeltaV MES

Syncade (DeltaV)

Tulip

Job description

Lilly is pursuing a MES Engineer to join the API Manufacturing Site in Houston, Texas. The role supports design, development, delivery, and validation of the DeltaV MES solution to meet site operational, quality, and compliance needs.

You will work with Operations, Quality, Engineering and IT to ensure successful deployment and ongoing support. Ideal candidates have 5+ years in MES, experience with DeltaV/Syn Cade, and familiarity with regulatory requirements (cGMP).