MES Engineer

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

Benefits offered by this job

401(k) plan

Pension program

Comprehensive benefits

Job summary

Lilly in Houston, TX is seeking an experienced MES Engineer to lead DeltaV MES implementation, validation, and startup for a new API manufacturing site. You will design, configure, and support MES workflows, electronic batch records, and interfaces across Operations, Quality, and IT to ensure compliant, reliable manufacturing processes.

You will partner with site teams to drive readiness activities, validate MES capabilities, and support go-live with strong cross-functional collaboration,

Qualifications

• Bachelor’s degree in IT, engineering, or related field.
• 5+ years with MES system design, implementation, and validation.
• 3+ years in regulated pharmaceutical or medical device manufacturing environments.
• Authorized to work in the United States on a full-time basis.

Responsibilities

• Partner with site teams to gather requirements and author/validate electronic batch records.
• Support MES startup activities including configuration of recipes and workflows.
• Configure electronic logbooks and Weigh & Dispense interfaces.
• Integrate MES with ERP, Historian, DCS, and equipment via Edge tech.
• Conduct site testing and validation (IQ/OQ/PQ) to ensure readiness.
• Generate CSV documentation for validation deliverables.
• Troubleshoot MES issues with cross-functional teams.
• Support go-live and hypercare activities.
• Ensure compliance with GSOPs, CSV standards, and 21 CFR Part 11.

Skills

DeltaV MES

GxP compliance

Regulatory knowledge

Communication skills

Education

Bachelor’s degree in IT/Engineering

Tools

Emerson DeltaV

Job description

At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work—but it’s work worth doing. If you’re driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us.

MES Engineer

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 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.

Lilly is investing $6.5 billion to build a new state-of-the-art active pharmaceutical ingredient (API) manufacturing site at Generation Park in Houston, Texas. The new site will produce APIs for small-molecule medicines for cardiometabolic health and will be built with the latest high-tech equipment, highly integrated and automated manufacturing systems, and a focus on minimizing environmental impact. This is a once-in-a-lifetime opportunity to help build and start up a new site.

What You'll Be Doing

The MES Engineer is part of the new API facility's MES team, supporting the design, development, delivery, and computer system validation of DeltaV MES solution. You will implement, configure, and support the MES solution to meet the site's operational, quality, and compliance needs — working closely with Operations, Tech Services, Engineering, Quality, and the broader Tech at Lilly team to ensure successful deployment and long-term support of MES capabilities.

Your Primary Responsibilities

• Partner with site teams to gather requirements, define digital workflows, and author/validate electronic batch records aligned with operational processes.
• Support MES startup activities, including configuration of MES recipes, workflows, electronic work instructions, and electronic batch records (EBRs).
• Configuration of electronic logbooks (Equipment Tracking) and Weigh & Dispense
• Configuration of MES interfaces with other manufacturing systems (ERP system, Historian, DCS, Manufacturing Equipment via Edge technology, etc)
• Implement and support site-level testing and validation efforts (e.g., Installation Qualification, Performance Qualification) to ensure system readiness.
• Generation of associated CSV (Computer System Validation) documentation
• Troubleshoot MES issues and collaborate with multi-functional teams to resolve system or process gaps.
• Support site readiness and go-live efforts, including hypercare support and frontline troubleshooting.
• Ensure compliance with Lilly Global Standard Operating Procedures (GSOPs) and Computer System Validation (CSV) standards, including 21 CFR Part 11 and GAMP 5.
• Develop and maintain system documentation, SOPs, training materials, and support guides
• Collaborate with global/site MES architects and platform teams to align on standards, design, and configuration best practices.

What You Should Bring

• Pharmaceutical Manufacturing Regulatory compliance knowledge and experience (cGMP)
• Experience with DeltaV MES (Previously known as Syncade) Recipe Authoring and validating Master Batch Records (MBRs) in a regulated environment.
• Strong analytical and problem-solving skills across applications, configurations, and integrations.
• Excellent communication skills, with the ability to articulate complex technical concepts to non-technical audiences.
• Ability to work closely with Operations, Quality, Engineering, and IT teams to translate operational needs into executable MES solutions.
• Experience with tier-one MES platforms, in particular Emerson Syncade/DeltaV.

Your Basic Qualifications

• Bachelor’s Degree in IT, Engineering, or related technical field,
• 5+ years experience with MES system design, implementation, and validation.
• 3+ years of experience in regulated pharmaceutical or medical device manufacturing environments.
• Qualified applicants must be authorized to work in the United States on a full-time basis. Lilly will not provide support for or sponsor work authorization or visas for this role, including but not limited to F-1 CPT, F-1 OPT, F-1 STEM OPT, J-1, H-1B, TN, O-1, E-3, H-1B1, or L-1.

Additional Preferences

• Prior experience with no-code/low-code frontline platforms, in particular Tulip, and with distributed control systems such as Emerson DeltaV, including recipe and batch interfaces to MES.
• Strong documentation skills and attention to detail, with experience in generating validation deliverables and training materials.
• Professional experience working in a GxP regulated environment.
• Experience commissioning and qualifying systems at a new site, and supporting API, small molecule, oligonucleotide, or synthetic chemistry operations.

Other Information

• Role is based onsite at Houston, Texas – API Manufacturing Site

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 proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, 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 are open to all employees. Our current groups include: Africa, Middle East, Central Asia (AMECA), Black Employees at Lilly (BE@Lilly), Chinese Culture Network (CCN), EnAble, Evolve, Lilly Indian Network (LIN), Organization of Latinx at Lilly (OLA), Pride (LGBTQ+ Allies), Veterans Leadership Network (VLN) and Women’s Initiative for Leading at Lilly (WILL).

Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is

$66,000 - $158,400

Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities). Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly’s compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.

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