- Hyderabad, Telangana, India
- Full-time · Associate
- 3–5 years
Experienced MES professional responsible for recipe authoring, validation, and production support across manufacturing sites.
Responsibilities
- Author, configure, and maintain MES recipes — including Generic Master Batch Records (GMBR) and Production Master Batch Records (PMBR) — on PharmaSuite or Werum PAS-X platforms
- Support MES recipes in production, including troubleshooting, making changes, and ensuring recipe integrity during live operations
- Manage recipe migration and promotion across environments (Dev → Test/QA → Validation → Production) following change control processes
- Perform end-to-end recipe validation, including test script authoring, execution, 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
Requirements
- Bachelor's degree in Engineering, Life Sciences, Computer Science, or related field
- Nice to have: global pharmaceutical manufacturing IT/MES deployment team experience
- Nice to have: change control and deviation management processes in a validated environment