Plant Head, Padra

Position Summary We are seeking an exceptional leader to drive operational excellence, scale manufacturing capabilities, and achieve global competitiveness while ensuring compliance with CDSCO, EMA, and EU MDR requirements. Key Responsibilities Oversee end-to-end manufacturing operations across all sterile/aseptic product linesScale production capacity to support 2X revenue growth through CMO partnerships and captive expansion Drive Industry 4.0 transformation: automation, IoT, MES, data analytics, and AI-driven optimization Ensure GMP compliance and maintain the highest quality standards Manage CDSCO, EMA, EU MDR, and international regulatory audits with zero critical observationsLead capacity expansion, technology transfers, and new product introductions Develop and manage CMO relationships while optimizing captive production capabilities Support export market expansion through compliance excellence and production scalability Implement Lean Manufacturing, Six Sigma, and continuous improvement initiativesBuild and develop high-performing production teams across multiple shifts Establish competitive benchmarking systems and drive market leadership in quality and efficiency Required Experience&Skills Manufacturing Expertise 12-18 years in pharmaceutical manufacturing with 5-7 years in leadership roles Extensive experience with sterile/aseptic operations (PFS, vials, LVP, SVP) Track record with ophthalmic or injectable product manufacturing Experience with CMO operations and capacity scaling strategiesPreferred: Experience with top-tier companies Industry 4.0&Technology Proven experience leading digital transformation in pharmaceutical manufacturing Expertise in automation, MES, SCADA, IoT, data analytics, and AI/ML applications Regulatory Compliance Extensive CDSCO inspection and compliance experience (Schedule M requirements) Strong track record with FDA inspections and surveillance auditsIn-depth experience with CE marking, PMA/ MAA, and Notified Body audits Technical Competencies Deep understanding of GMP, aseptic processing, and sterility assurance Knowledge of validation protocols, process validation, and risk management (FMEA, HACCP) Strong leadership, strategic thinking, and change management capabilities