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
Qualifications
- 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.
