Manager , MES - SME
Listed on 2026-10-30
-
IT/Tech
IT Business Analyst, Systems Analyst, IT Support, IT Consultant
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Company:
Sun Pharmaceutical Industries Ltd
Manager, MES – SME
Job Grade (refer to JE)G11A
Function:Global IT
Sub-function:Manufacturing IT
Location:Job Summary
At Sun Pharma, we commit to helping you “Create your own sunshine”—by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community.
Are You Ready to Create Your Own Sunshine?As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.”
Job Summary:We are seeking a seasoned professional with 6-8 years of experience in the pharmaceutical industry, including technical and functional experience in MES & L2 systems.
Site SME – MES ProjectThe Site SME – MES Project is a key functional and technical expert responsible for supporting the successful implementation of the Manufacturing Execution System (MES) & L2 at the Halol & Baska pharmaceutical manufacturing sites. This role ensures that site-specific manufacturing processes are accurately captured and reflected in the global MES solution.
The SME is also accountable for leading site-level validation activities and technical owner responsibility
, and managing all GxP documentation related to the MES & L2 system. The Site SME is the go-to authority for end-to-end MES product knowledge. This includes a deep understanding of system functionality, configuration, and compliance requirements.
The SME also serves as the first point of contact for any MES front-end application issues, supporting users in troubleshooting, training, and ongoing system usage post-go-live. The ideal candidate will ensure adherence to global regulations (FDA 21 CFR Part 11, EU GMP, GAMP5)
Previous experience with Werum (Korber Pharma) for pharma industry is a big plus
Areas Of Responsibility:- MES Implementation: Representing site-specific needs during MES design, configuration, and deployment.
- Validation Leadership: Leading IQ, OQ, PQ, UAT, and traceability matrix execution.
- Documentation Ownership: Managing GxP documentation (URS, FS, DS, test cases, validation plans/reports).
- MES Product Expertise: Maintaining deep knowledge of MES functionality and architecture.
- Front-End Support: Acting as the first point of contact for MES application issues and user support.
- Training & Adoption: Delivering training and ensuring user readiness for MES usage.
- Data Management: Supporting data collection, migration, and master recipe creation.
- Audit Readiness: Ensuring all documentation and systems are compliant and audit-ready.
Global MES Program Team: Collaborating to align site processes with global standards and system templates.
Quality Assurance (QA) & QA IT: Ensuring validation and compliance with GxP and CSV standards.
Business Users: Engaging with production, quality, and operations teams for requirements gathering and support.
Engineering & IT Teams: Coordinating technical aspects of MES deployment and integration.
Site Leadership :
Providing updates on MES implementation, validation status, and issue resolution.
End Users: Supporting MES usage, troubleshooting front-end issues, and providing training.
External Interactions (outside the organization)MES Vendors & Consultants: Participating in workshops, configuration sessions, and demos; resolving technical issues.
Auditors & Regulatory Bodies: Supporting audits by ensuring system and documentation compliance.
Third-Party Validation Experts: Collaborating on validation strategy…
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