Role Overview :

We are looking for an experienced Opcenter Execution Pharma / SIMATIC IT eBR Techno-Functional Lead to drive MES requirements, solution design, configuration, validation, and implementation for pharmaceutical manufacturing environments. The role involves close collaboration with Business SMEs, Key Users, MES Engineers, customer stakeholders, and management teams to deliver compliant and scalable MES solutions.

Key Responsibilities :

- Understand and analyze pharmaceutical manufacturing processes and translate business requirements into MES solutions.

- Interact with Business SMEs and Key Users to gather, analyze, and validate requirements.

- Design Process Instructions (PIs) based on site-specific manufacturing requirements.

- Identify common processes across multiple manufacturing sites and design Global Process Instructions for reuse and standardization.

- Work closely with MES Engineers for solution design, configuration, testing, and implementation.

- Perform validation of Process Instructions and ensure solutions meet business and compliance requirements.

- Prepare and review project documentation, including URS, FRS, Design Specifications, Test Scripts, and validation-related documentation.

- Lead the MES functional team, allocate tasks, monitor progress, and provide technical/functional guidance.

- Coordinate with customer and internal stakeholders and provide regular project status updates to management.

- Support continuous improvement and standardization of MES processes across manufacturing sites.

Essential Skills :

- Strong techno-functional expertise in Opcenter Execution Pharma / SIMATIC IT eBR.

- Strong understanding of pharmaceutical manufacturing processes.

- Hands-on experience designing and validating Process Instructions (PIs).

- Experience identifying common manufacturing processes and developing Global PIs.

- Strong requirements gathering and business stakeholder management skills.

- Experience with MES configuration, testing, and validation.

- Good understanding of GxP / pharmaceutical validation requirements.

- Strong experience in preparing URS, FRS, Design Specifications, Test Scripts, and related documentation.

- Proven ability to lead teams, assign work, and track delivery.

- Excellent communication and collaboration skills with business and technical stakeholders.