Business Partner

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 Roles Responsibilities You will be responsible for validation and analytical method transfers of IP In-Process FP Finished Product API Active Pharmaceutical Ingredient Excipients and Packing materials You will initiate and investigate CRN Change Request Notice Incidents OOT Out of Trend and OOS Out of Specification You will be responsible for approval of STPs Standard Testing Procedures Specifications SOPs Standard Operating Procedures Protocols and Analytical test reports You will ensure Good laboratory practices Safety practices Good documentation practices and ensure the cleanliness of the laboratory Your role involves ensuring the maintenance preparation procurement of laboratory standards and chemicals solvents as per the laid down procedures You will participate and organize equipment instrument Qualifications change control mechanism and procurement of laboratory requirements You will ensure calibration performance verification of analytical instruments and equipment as per master schedule You will be responsible for preparation of response for Internal and external audits and other QMS Quality Management System related activities Your responsibilities will include ensuring compliance in LIMS Laboratory Information Management System related activities and ensuring that all the QMS documents are investigated timely reviewed and appropriate CAPA s Corrective and Preventive Actions are taken and implemented Qualifications Educational qualification An M Sc degree in Chemistry Analytical Chemistry or a related field Minimum work experience 10 to 12 years of experience Skills attributes Technical Skills Expertise in method validation and analytical method transfers for IP FP API Excipients and Packing materials Knowledge of calibration and performance verification of analytical instruments and equipment as per the master schedule Experience in ensuring the maintenance preparation and procurement of laboratory standards chemicals and solvents according to established procedures Participation and organization of equipment instrument qualifications and change control mechanisms Procurement expertise for laboratory requirements Behavioural Skills Attention to detail and commitment to ensuring compliance with QMS documents including OOS OOT and Incident investigations Ability to respond to internal and external audits and participate in other QMS-related activities Strong organizational skills for LIMS related activities Effective communication and collaboration skills for coordinating and implementing CAPAs 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 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 catalyze 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 For more details please visit our career website at