MES Recipe Author Associate

Eli Lilly and Company

Hyderabad

On-site

INR 900,000 - 1,700,000

Full time

4 days ago
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Job summary

Eli Lilly and Company is seeking an experienced MES professional to join the MES deployment team in Hyderabad. The role focuses on recipe authoring, validation, and production support across manufacturing sites.

The ideal candidate has 3–5 years of MES recipe experience and hands‑on work with PharmaSuite or Werum PAS‑X, ensuring compliance with GxP and CSV requirements throughout the lifecycle of recipes.

Qualifications

  • 3–5 years of experience in MES recipe authoring and support.
  • Hands‑on experience with PharmaSuite or Werum PAS‑X MES platforms.
  • Practical exposure to GMBR and PMBR authoring and lifecycle management.
  • Experience moving/deploying recipes across multiple environments.
  • Working knowledge of recipe/system validation practices.

Responsibilities

  • Author, configure, and maintain MES recipes on PharmaSuite or Werum PAS-X platforms.
  • Support MES recipes in production, including troubleshooting and ensuring recipe integrity during live operations.
  • Manage recipe migration and promotion across environments following change control processes.
  • Perform end‑to‑end recipe validation, including test script authoring and documentation in line with GxP/CSV requirements.
  • Collaborate with cross‑functional MES deployment engineers to plan and execute recipe releases and site go‑lives.
  • Provide L2/L3 support for recipe‑related incidents, performing root cause analysis and implementing corrective/preventive actions.
  • Ensure all recipe changes comply with data integrity requirements.
  • Partner with Manufacturing, Quality, and Validation teams to align recipe design with process and compliance needs.
  • Maintain accurate documentation for authored/modified recipes.

Skills

MES experience
Process validation
GxP awareness
Troubleshooting
Documentation

Education

Engineering/Life Sciences/CS degree

Tools

PharmaSuite
Werum PAS-X

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. We are looking for an experienced MES professional to join our MES deployment team, responsible for recipe authoring, validation, and production support across manufacturing sites.

Responsibilities
  • Author, configure, and maintain MES recipes on PharmaSuite or Werum PAS-X platforms.
  • Support MES recipes in production, including troubleshooting and ensuring recipe integrity during live operations.
  • Manage recipe migration and promotion across environments following change control processes.
  • Perform end‑to‑end recipe validation, including test script authoring and documentation in line with GxP/CSV requirements.
  • Collaborate with cross‑functional MES deployment engineers to plan and execute recipe releases and site go‑lives.
  • Provide L2/L3 support for recipe‑related incidents, performing root cause analysis and implementing corrective/preventive actions.
  • Ensure all recipe changes comply with data integrity requirements.
  • Partner with Manufacturing, Quality, and Validation teams to align recipe design with process and compliance needs.
  • Maintain accurate documentation for authored/modified recipes.
Requirements
  • 3–5 years of experience in MES recipe authoring and support.
  • Hands‑on experience with PharmaSuite or Werum PAS‑X MES platforms.
  • Practical exposure to GMBR and PMBR authoring and lifecycle management.
  • Experience moving/deploying recipes across multiple environments.
  • Working knowledge of recipe/system validation practices.
  • Experience in a production support role within a regulated manufacturing environment.
  • Understanding of GxP, CSV/GAMP 5, and pharmaceutical manufacturing quality processes.
  • Strong troubleshooting and root‑cause analysis skills.
  • Good communication skills to work with global/cross‑site manufacturing and quality teams.
  • Preferred: Prior experience working within a global pharmaceutical manufacturing IT/MES deployment team.
  • Preferred: Exposure to change control and deviation management processes in a validated environment.
  • Preferred: Bachelor's degree in Engineering, Life Sciences, Computer Science, or related field.
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