Team Member

Company DescriptionDr Reddys 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 Cant 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 transparencyDr Reddys 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 Quality Assurance TeamWe are seeking an individual for the Quality Assurance team responsible for ensuring line clearance material verification and conducting in-process checks according to batch manufacturing and packing records The role includes timely sampling testing coordination in cleaning validation and ensuring compliance with technology transfer and exhibit batches including the review and certification of batch records Roles Responsibilities You will be responsible for performing line clearance material verification start-up checks and in-process checks as per the batch manufacturing record and batch packing record Responsible for technology transfer process validation and compliance to the validation master plan You will be responsible for handling of cleaning validation monitoring of sampling and compliance You will implement and comply with Technology Transfer and initiation of exhibit batches with monitoring of validation batches Vendor qualification and management at site QualificationsEducational QualificationA Bachelors degree in Pharmacy Chemistry Chemical Engineering or a related fieldMinimum Work Experience5 to 10 years of experience in pharmaceutical manufacturing or a similar roleSkills Attributes Technical Skills Process and cleaning validation activities sampling and relevant standards Proficiency in performing line clearance material verification start-up checks and in-process checks following batch manufacturing and packing records experience on cGMP activities Behavioural Skills Attention to detail in performing line clearance verification and record reviews Skilled in time management and coordination for sampling testing and execution of batch manufacturing and packing activities Communicates effectively with team members and stakeholders regarding batch-related activities and compliance able to work in full load condition with CFT Additional InformationAbout the DepartmentGlobal 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 OfferedAt Dr Reddys we actively help to catalyze your career growth and professional development through personalised learning programs The benefits you will enjoy at Dr Reddys 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 CultureAsk any employee at Dr Reddys why they come to work every day and theyll say because Good Health Cant Wait This is our credo as well as the guiding principle behind all our actions For more details please visit our career website at