
Mes Co-ordinator
3 weeks ago
**Title**:MES Co-ordinator**:
- Date: Jul 10, 2025
- Location: Halol 1 - Information Technology
- Company: Sun Pharmaceutical Industries Ltd
**Job Classification Code**
**Job Classification Label**
**Job Title**:
Manager, MES & L2 project coordinator**Job Grade**(refer to JE)G10**Function**:
Global IT**Sub-function**:
Manufacturing IT**Manager’s Job Label**:
**Skip Level Manager’s Label**:
**Function Head Title**:
**Location**:
Halol/Baska**No. of Direct Reports (if any)**
0**Business Unit**:
**Job Summary**
We are seeking a seasoned professional with 7-9 years of experience in the pharmaceutical industry, including hands-on expertise in Manufacturing Execution Systems (MES) and L2 integration.The **Site Project coordinator for MES Implementation** will be the primary coordinator for all MES-related activities at the Halol / Baska sites. This role demands dedicated full-time support to the project to ensures smooth execution, alignment with the global MES strategy, and timely delivery of milestones to enhance manufacturing efficiency, compliance, and digital transformation. The role will work closely with internal teams—including QA, IT, SAP, business users, and L2 integration—as well as external vendors and infrastructure leads.- **Previous experience with Werum (Korber Pharma) for pharma industry is a big plus**
**Areas Of Responsibility**
Project Coordination:
Lead and coordinate all MES implementation activities at the site, ensuring alignment with the global MES strategy.Stakeholder Management:
Serve as the single point of contact for site-level stakeholders, including QA, QA IT, IT, SAP, and business users (Production & Engineering)Vendor & Partner Collaboration:
Work closely with MES vendors, infrastructure teams, and integration partners to ensure smooth execution.Timeline & Risk Management:
Manage project schedules, track milestones, identify risks, and implement mitigation plans.Infrastructure & Readiness:
Ensure site infrastructure (network, servers, systems) is ready and validated for MES deployment.Compliance & Validation:
Oversee adherence to site quality standards, IT validation (CSV), and regulatory requirements.Communication & Reporting:
Maintain clear and timely communication with the Global Project Manager and other stakeholders; provide regular updates and escalate issues as needed.Change Management:
Facilitate change control processes and support user readiness and adoption.**Travel Estimate**
Less**Job Scope**
**Internal Interactions (within the organization)**
Global Project Manager - MES ProgramSite QA and QA IT teamsSite IT and Infrastructure teamsProduction, Operations teamsSAP CoordinatorsSite SME and Global SME**External Interactions (outside the organization)**
MES vendors and implementation partnersSystem integrators (L2/PLC/SCADA)Infrastructure service providers (network/server)Validation consultants (if outsourced)Auditors (during validation or compliance reviews)**Geographical Scope**
Halol/Baska site**Financial Accountability (cost/revenue with exclusive authority)**
No direct financial authority**Job Requirements**
**Educational Qualification**
Bachelor’s degree in Engineering, Information Technology, Computer Science, Production, Pharmaceutical Sciences, or a related technical field.Preferred: Master’s degree (e.g., MBA, M.Tech, M.Pharm) with specialization in Project Management, Operations Management, Industrial Automation, or Pharmaceutical Technology.**Specific Certification**
PMP - for structured project execution (preferred)GAMP5 or CSV Training - for compliance in regulated environments**Experience**
7-9 years of experience managing IT or digital transformation projects, preferably in pharmaceutical manufacturing.Hands-on experience with MES platforms, L2/PLC systems, and SAP integration and Edge Cloud IoT.Proven track record in project planning, stakeholder coordination, and cross-functional team leadership.Strong background in GxP compliance, CSV, and validation protocols (IQ/OQ/PQ).Experience working on the shop floor and with QA, IT, and business teams in a regulated environment.**Skill (Functional & Behavioural)**:
**Functional**:Strong project management expertise in IT/digital systems, Knowledge of MES platforms, L2/PLC systems, and SAP integration, Familiarity with GxP, CSV, and validation protocols (IQ/OQ/PQ), Understanding of pharmaceutical manufacturing processes and shop floor operations, Proficiency in stakeholder coordination and cross-functional collaboration**Behavioral**: Strong communication and interpersonal skills, Proactive problem-solving and risk management, High attention to detail and compliance mindset, **Ability to work under pressure** and manage multiple priorities, Team-oriented with a focus on collaboration and accountability**Additional Skills: (Good to have)**
Knowledge of data analytics toolsEdge Cloud deployment experience with (IoT and and IIoT)L2 integration with MESMES integration with SAPUnderstanding of network and