Company 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 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 Qualifications 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 Additional Information 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 productive 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 to help patients lead healthier lives and we re always attuned to the new and the next to empower people to stay fit And to do this we foster a culture of empathy and dynamism People are at the core of our journey over the last few decades They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success We believe that when people with diverse skills are bound together by a common purpose and value system they can make magic For more details please visit our career website at

📌 Team Member - Production (Visakhapatnam)
🏢 Dr. Reddy's Laboratories
📍 Visakhapatnam