Team Member

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 an individual for the SIT Team to oversee the investigations working closely with Cross-Functional Team CFT members to identify root causes and implement corrective and preventive actions The role involves active participation in investigating Out of Specification OOS cases ensuring accurate classification in the DCMS incident or SAP log and providing support during regulatory inspections Roles Responsibilities You will be responsible for overseeing the investigations of deviations from the outset collaborating closely with Cross-Functional Team CFT members to identify root causes corrective actions CA preventive actions PA and preparing comprehensive reports Your role involves active participation in investigating valid OOS Out of Specification and other relevant cases working closely with CFT members to determine root causes CA PA and report writing You will review level Minor Investigation required Major and Critical incidents providing constructive feedback for improvement Your responsibilities include periodically assessing the trending of level deviations highlighting or escalating key observations regularly reviewing the DCMS log or SAP OOS log to ensure accurate classification and utilizing the Rubrics template for crafting investigation reports You will offer necessary support to the site in readiness for or during regulatory inspections related to investigations Qualifications Educational qualification A Bachelor s or Master s degree in a relevant scientific field such as Chemistry Biochemistry Pharmacy or related discipline Minimum work experience 5 to 10 years of experience in a pharmaceutical or related industry with a focus on investigations and quality assurance Skills attributes Technical Skills In-depth knowledge and experience in overseeing investigations and familiarity with root cause analysis corrective actions CA and preventive actions PA Expertise in investigating valid OOS and other relevant cases Familiarity with reviewing deviations log and ability to perform classification of data Ability to craft comprehensive investigation reports Experience in providing necessary support for regulatory inspections related to investigations Knowledge of regulatory requirements pertaining to incident investigations Behavioural Skills Ability to collaborate closely with CFT members Analytical mind set for identifying root causes and developing effective solutions Strong problem-solving skills and attention to detail in reviewing incidents reports and trending data and implementing corrective actions Effective communication skills for report writing and escalation of key observations Commitment to ensuring compliance with regulatory requirements in investigations Ability to offer necessary support to the site in readiness for or during regulatory inspections 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 he 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 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 https careers drreddys com