Manager 2, MES - SME

Job description

Job Title

Manager, MES – SME Job Grade (refer to JE)

G11A Function

Global IT Sub-function: Manufacturing IT Location: Baska

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.”

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. The 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. Travel Estimate Less Job Scope Internal Interactions (within the organization)

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 and execution if outsourced.

External Support Teams

Engaging with vendor support for MES application troubleshooting and escalations.

Geographical Scope Primary Sites

Halol and Baska manufacturing sites 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 Industrial Automation, Pharmaceutical Technology or related technical fields Specific Certification GAMP 5 – for system validation in regulated environments. CSV (Computer System Validation) – for compliance with GxP. MES Platform Certifications – e.g., Werum PAS-X, Siemens Opcenter, or Rockwell 21 CFR Part 11 Compliance Training – for electronic records and signatures.

Experience

Pharmaceutical Manufacturing: Strong understanding of pharma shop floor operations and regulatory requirements.

MES or Digital Systems

Prior hands-on experience with MES platforms or similar systems in GxP-regulated environments.

Validation Expertise

Proven experience in validation documentation and execution, especially for GxP Category 4 & 5 systems.

Application Support

Experience in resolving front-end MES issues and supporting end-users post-deployment.

Audit Experience

Familiarity with audit processes and documentation expectations Skill (Functional & Behavioural): Functional: MES system configuration, deployment, and validation, Front-end application troubleshooting and user support, GxP and 21 CFR Part 11 compliance, Validation protocol development and execution (IQ, OQ, PQ, UAT), Documentation management (URS, FS, DS, traceability matrices), Data migration and master recipe creation

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, Detail-oriented with a focus on compliance and quality, Proactive problem-solving and decision-making, Comfortable working on the shop floor and in technical environments Additional

Skills: (Good to have) Knowledge of data analytics tools Edge Cloud deployment experience with (IoT and and IIoT) L2 integration with MES MES integration with SAP Understanding of network and databases Your Success Matters to Us At Sun Pharma, your success and well-being are our top priorities!

We provide robust benefits and opportunities to foster personal and professional growth. Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let’s create a brighter future together!

Disclaimer

The preceding job description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of the incumbent(s).