Expert Project Design

Job description

Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can’t Wait. We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries. For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolves and undergoes disruption, we see an opportunity – to strengthen our core further (the next steps) and to build the future (the new bets). ‘The Next and the New’ is how we aim to continue to be the partner of choice – purpose-driven, future-ready and sustainable. Our aim is to reach over 1.5 Bn+ patients across the world by 2030 by growing our core businesses and building for the future with sustainability at the core of our purpose and strategy. Sustainability for us means operating in a manner that respects people, planet and purpose – helping us conserve precious resources, serve our patients, create value for stakeholders, give back to society, fulfil our potential and maintain our integrity and transparency Dr Reddy’s maintains a work environment, free from discrimination and is an equal opportunity employer. We are committed to employ & nurture all qualified diverse workforce without regard to race, colour religion, nationality, sex, age, disability status, genetics, sexual orientation, gender expression, citizenship or any other characteristic or classification protected by applicable law(s) of the country we operate in. We treasure every talent, and recognize merit and diversity in our organization. Role Summary: We are seeking an Expert– Projects Design with strong expertise in formulation projects facility design, engineering, and oversee project execution. The role will be responsible for leading the planning, design, engineering, execution, commissioning, qualification, and operational handover of manufacturing facilities while ensuring compliance with global regulatory requirements and industry best practices. The ideal candidate will have extensive experience in Oral Solids, Oral Liquids, Topicals, Sterile Injectables, Aseptic Processing & Fill-Finish Facilities along with a proven track record of successfully delivering Greenfield, Brownfield, expansion, and modernization projects. Key Responsibilities 1. Project Planning & Governance Lead Conceptual, Basic and Detailed Engineering activities for formulation projects. Develop facility master plans, site development strategies, project roadmaps, and long-term manufacturing infrastructure plans. Prepare CAPEX estimates, project budgets, business cases, investment proposals, and project schedules &Manage project scope, cost, timelines, resources, and quality objectives. Deliver projects within approved budgets and timelines while maintaining compliance and quality standards. 2. Facility Design & Engineering Design GMP-compliant manufacturing facilities for OSDs, Oral Liquids, Topicals, Sterile Injectable Manufacturing, Aseptic Processing Facilities & Fill-Finish Facilities Develop facility concepts, process flow diagrams, block layouts, and detailed facility layouts. Optimize material, personnel, equipment, and waste flows to improve operational efficiency and regulatory compliance. Review URS, process requirements, engineering deliverables, and design documentation. Ensure designs comply with FDA, EU GMP, WHO GMP, ISPE & local regulatory requirements. 3. Greenfield, Brownfield & Capacity Expansion Projects Lead end-to-end project design & execution from concept development. Manage site selection inputs, facility planning, construction, commissioning, qualification. Execute modernization projects while minimizing impact on commercial operations. 4. Utilities, HVAC & Cleanroom Systems Design & review of HVAC, Clean Utility Systems including Purified Water (PW), Water for Injection (WFI), Pure Steam (PS), Clean Compressed Air, Process Gases Design review of Black Utility Systems including HVAC Utilities, Boilers, Chillers, Cooling Towers, Air Compressors, Fire Protection Systems, Drain & Industrial Water Systems Ensure compliance with ASME BPE, ISPE guidelines & pharmaceutical engineering standards. Develop facilities up to ISO 5 / Grade A & ensure environments ensuring pressure cascade philosophies, contamination control strategies, and airflow concepts. 5. Equipment Engineering Co-ordination & Qualification & Compliance Equipment selection & evaluations, procurement, installation & qualification activities. Review equipment layouts, utility requirements, and process integration requirements. Support and oversee DQ, IQ, OQ & PQ activities. Ensure facilities comply with FDA, EU, WHO, MHRA & applicable regulatory expectations. 6. Vendor, Contractor & Stake holder Management Evaluate and select EPC contractors, consultants, and equipment suppliers. Review vendor proposals, technical offers, and engineering deliverables. Monitor contractor performance, quality compliance, project schedules, and commitments. Participate in technical negotiations, and vendor development initiatives. Collaborate effectively with Production, QA, Validation, Automation, Engineering, SCM, Procurement, Finance, Regulatory Affairs, and SHE teams. 7. Operational Excellence, Automation & Sustainability Drive value engineering initiatives to optimize CAPEX and OPEX without compromising quality and compliance. Identify opportunities to improve facility efficiency, productivity, reliability & energy performance. Support automation, digitalization, and Industry 4.0 initiatives across manufacturing and utility systems. Provide engineering oversight for serialization, packaging automation, AMRs, ASRS, and smart manufacturing solutions. Promote Safety-by-Design principles and ensure compliance with EHS requirements. Participate in risk assessments, HAZOP studies, and sustainability initiatives including energy conservation, water management, and green building practices. Drive value engineering initiatives to optimize CAPEX and OPEX. Required Qualifications & Skills Education: Bachelor’s degree in mechanical engineering (B. Tech / B.E.) Experience: 6+ years of experience in Greenfield, Brownfield expansions of formulation facility design & execution. Technical Skills: Pharmaceutical Facility Design, Facility Master Planning, Utilities & Infrastructure Engineering, HVAC & Cleanroom Design, Qualification & Validation, Automation & Digitalization, CAPEX Planning & Cost Control, Risk Management, Engineering Change Management, Contamination Control, Regulatory Compliance, Vendor & Contractor Management Software Proficiency: AutoCAD, SAP, MS Project, Microsoft Office Additional Information Global Manufacturing Organisation (GMO) At Dr. Reddy's Laboratories, we are dedicated to making a meaningful impact on global healthcare through precision manufacturing and innovation. With a legacy of excellence, we are a leading force in the pharmaceutical industry. We operate 19 state-of-the-art manufacturing plants across Hyderabad, Vizag, Baddi, Mexico, Shreveport, and Mirfield, comprising 8 OSD facilities, 3 Injectables facilities, and 8 API facilities. Benchmarking manufacturing processes and continuous operational excellence are at the core of our capability to deliver quality medicines to our patients in 66 countries. We manufacture a portfolio of complex APIs and 1,150+ drug master files across key therapy areas such as Oncology, Cardio-vascular, Central Nervous System and Anti-Diabetes. he World Economic Forum has recognised our largest manufacturing facility in Bachupally, Hyderabad, as part of its Global Lighthouse Network. We aspire