Automation Strategy & Architecture • Define and implement standardized automation architecture across the facility, including PLC platforms, I/O configurations, communication protocols (e.g., OPC UA, Modbus, Ethernet/IP), and software frameworks. • Lead the integration of equipment and systems into centralized SCADA/DCS platforms ensuring interoperability and scalability. • Develop and enforce automation standards for new equipment and systems to ensure consistency and future-proofing. Vendor Identification & Management • Identify, evaluate, and onboard automation vendors and system integrators aligned with project goals and compliance requirements. • Drive tec • Drive technical discussions with vendors to ensure alignment with centralized architecture and integration capabilities. • Manage vendor performance during design, commissioning, and qualification phases. Touchless Operations & Robotics • Champion the implementation of touchless operations through robotics, automated guided vehicles (AGVs), and smart sensors.Lead automation initiatives in pharmaceutical manufacturing and packaging areas to reduce manual interventions and enhance compliance. • Collaborate with cross-functional teams to integrate robotics with MES, SCADA, and ERP systems. URS & Equipment Integration • Draft and review User Requirement Specifications (URS) with a focus on automation readiness and centralized system integration. • Ensure all new equipment is compatible with the facility’s automation standards and digital infrastructure complying all International Automation Standards. • Collaborate with engineering and operations teams to validate integration plans and execution. Data Management & Analytics • Establish data acquisition and historian systems for real-time monitoring and analytics. • Develop dashboards and reporting tools to visualize equipment performance, process KPIs, and compliance metrics n Jointly with Data Scientist and Lead Industry 4.0. • Utilize analytics to drive predictive maintenance, process optimization, and decision-making.Installation, Commissioning & Qualification • Oversee installation, commissioning, and qualification (IQ/OQ/PQ) of automation systems and integrated equipment. • Ensure all activities are executed within project timelines, budget, and regulatory frameworks. Compliance & Documentation • Ensure automation systems comply with USFDA, EU GMP, and ISO standards. • Maintain comprehensive documentation including validation protocols, SOPs, and audit trails. • Conduct periodic reviews and audits to ensure system reliability and data integrity. Continuous Improvement & Innovation • Stay abreast of emerging technologies in automation, robotics, and pharma manufacturing. • Drive continuous improvement initiatives to enhance operational efficiency and digital maturity. • Education • Bachelor’s/Master’s in Instrumentation, Automation, Electronics, or related engineering discipline.Qualifications Experience • Minimum 7–8 years in pharmaceutical or API manufacturing automation, preferably in greenfield projects. • Direct experience in DCS OEM’s like Siemens, Emerson etc. working for pharma client can be preferred • Proven experience in implementing DCS, SCADA, PLC, and robotics systems. • Hands-on experience in equipment integration, vendor management, and automation standardization. • Exposure to peptide, bulk drug, or injectable manufacturing environments is preferred. Skills • Strong knowledge of automation platforms (Siemens, Rockwell, Schneider, etc.), industrial protocols, and software tools. • Expertise in drafting URS and managing automation lifecycle. • Excellent project management and stakeholder engagement skills. • Analytical mindset with proficiency in data visualization and reporting. • Passion for innovation, digital transformation, and operational excellence.