MES Engineer – GMP Digital Manufacturing

Eli Lilly and Company

Concord (NC)

On-site

USD 66,000 - 158,000

Full time

2 days ago
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Job summary

Lilly in Concord, NC seeks a MES Engineer to support, develop and deploy manufacturing execution systems and equipment for GMP environments, translating business needs into IT solutions.

The role focuses on compliance, validation, and collaboration with global teams to optimize digital tickets and MES workflows on site. Expect 10-15% travel, on-call duties, and a strong emphasis on quality and regulatory requirements.

Qualifications

  • Bachelor of Science degree in IT, Chemistry, Pharmacy, Science, Engineering, or related field.
  • 2+ years of relevant work experience in information technology, engineering, business support or related areas.
  • Experience working with a MES in GMP setting (e.g. PharmaSuite).
  • Ability to effectively communicate with business stakeholders and IT subject matter experts, understanding and speaking the language of both.
  • Qualified applicants must be authorized to work in the United States on a full-time basis. Lilly will not sponsor work authorization or visas for this role.

Responsibilities

  • Understand manufacturing processes and translate into IT requirements for MES.
  • Support and deploy MES applications to meet business needs.
  • Ensure regulatory, legal, or quality requirements are complied with.
  • Collaborate with Global next generation MES team and third parties during validation.
  • Lead delivery and support of digital solutions from the site perspective.
  • Manage site agenda and workload to ensure timely delivery.

Skills

Effective communication
Problem solving
Regulatory awareness
Influence without authority

Education

Bachelor of Science in IT/Engineering/related field

Tools

PharmaSuite

Job description

Lilly in Concord, NC seeks a MES Engineer to support, develop and deploy manufacturing execution systems and equipment for GMP environments, translating business needs into IT solutions.

The role focuses on compliance, validation, and collaboration with global teams to optimize digital tickets and MES workflows on site. Expect 10-15% travel, on-call duties, and a strong emphasis on quality and regulatory requirements.

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