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Job Summary We are looking for a candidate to oversee manufacturing and production operations, managing equipment, process validation, handling change controls, deviations, incidents, and ensuring compliance with regulatory audits. Responsibilities include creating SOPs (Standard Operating Procedure), providing training, and applying expertise. " Roles & Responsibilities You will be responsible for handling line operations, specifically production and manufacturing activities like CIP (Cleaning-in-place), SIP (Sterilizing-in-place), and batch manufacturing. You will be responsible for handling equipment like Steam Sterilizer, Dry heat sterilizer, HVAC (Heating, Ventilation, and Air Conditioning), water system, compressed air, Nitrogen system, etc. You will be responsible for process validation for Sterilization, Washing, Aseptic filling, and cleaning procedures. You will evaluate change controls, deviation, and incident, (OOS) out of specification, (OOT) out of trend, and risk management. You will prepare the production process SOPs (Standard Operating Procedures) and batch records. You will provide training on GMP (good manufacturing practices). You will apply knowledge of aseptic processes, Lean, OEE (Overall Equipment Effectiveness), and similar KPIs (Key Performance Indicators). You will respond to queries and questions regarding regulatory audits such as US FDA (Food and Drug Administration). " Educational Qualification A Bachelor's or Master's degree in Pharmaceutical Sciences, Chemical Engineering, or a related field Minimum Work Experience 7 years of experience in pharmaceutical manufacturing operations Skills & Attributes Technical Skills Expertise in line operations, especially in manufacturing activities like CIP, SIP, and batch manufacturing. Proficiency in understanding equipment such as Steam Sterilizer, Dry heat sterilizer, HVAC, water system, compressed air, Nitrogen system, etc. Understanding of Process Validation for Sterilization, Washing, Aseptic filling, and cleaning procedures. Knowledge for evaluation of change control, deviation, incident, out of specification, out of trend, and risk management. Experience in preparing production process SOPs and batch records. Understanding and application of Aseptic processes, Lean, OEE, and similar KPIs. Hands-on experience in regulatory audits, particularly with agencies like the US FDA. Good understanding of GMP and good laboratories practice. Behavioural Skills Capacity to provide training on GMP and other relevant areas. Collaborates seamlessly with cross-functional teams, promoting a cooperative and inclusive work environment. Efficiently manages time to meet production schedules and deadlines without compromising quality. Must have hands-on experience in sophisticated manufacturing machines and equipment. Effective communication and training skills for user departments and service providers. " About the Department - 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. The World Economic Forum has recognised our largest manufacturing facility in Bachupally, Hyderabad, as part of its Global Lighthouse Network. We aspire to be the most efficient pharma operations in the world. Our productivity improvement and digitalisation efforts are key to staying competitive, meeting business imperatives, and meeting our ambitious ESG goals. Building such 'factories of the future' is integral to innovation and to build healthcare of the future. " Benefits Offered At Dr. Reddy's, we actively help to catalyse your career growth and professional development through personalised learning programs. The benefits you will enjoy at Dr. Reddy's are on par with the best industry standards. They include, among other things and other essential equipment, joining & relocation support, family support (Maternity & Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself. " Our Work Culture Ask any employee at Dr. Reddy's why they come to work every day and they'll say, because Good Health Can't Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means

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