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 transparencyJob DescriptionJob SummaryWe are seeking a dynamic Formulation Scientist in BRaIN for designing and development of formulation, process, and ensure seamless end to end product development.Roles & Responsibilities You will be responsible for the development for robust, effective and bioequivalent drug product in timely manner adhering to safety and quality standards. Also provide support in documentation for regulatory submissions. You will be responsible to co-ordinate closely with analytical team to devise effectiveProof of Concept (POC). You will be responsible to support in scale-up to pilot/plant scales for OSD Products. You will be responsible for performing pre-formulation studies for material characterization, drug-excipient compatibility and Reference Listed Drug (RLD) characterization (including reverse engineering, formulation designing and optimization,processes designing and scale up). You will be responsible for preparation of risk evaluation and risk mitigation documents, Scale-up batch documents, and filing documentsfor drug product at every stage of development. You will be responsible to review data generated and participate in discussions with experts to conclude on prototype(s). Participate in strategizing the sourcing of Active Pharmaceutical Ingredient (API), raw materialsand ensure development studies are performed related to regulatory and internal system requirements.QualificationsEducational qualification: Masters in Pharmaceutical/M.Tech in Chemical EngineeringMinimum work experience: 5 to 7 years of experience in handling multi vitamin Oral dosage forms in pharmaceutical industry.Skills & attributes:Technical Skills Have work experience on Formulation Development and expertise in multivitamin dosage forms. Experience in pharmaceutical development of multivitamin tablets by Quality by Design (QbD). Knowledge on Good Manufacturing Practice and Good Laboratory Practice.Behavioral Skills Excellent communication and interpersonal skills. Strong analytical and problem-solving abilities. Ability to work collaboratively with own team and cross-functional teams.Additional InformationAbout the DepartmentIntegrated Product Development OrganisationWe integrate our deep science capabilities and cutting-edge technology to develop innovative, accessible and affordable therapies for patients worldwide. We are a science-driven, innovation-focused pharmaceutical company committed to accelerating access to healthcare solutions to patients around the world. We have End to end capabilities in API, Formulations, Clinical, Intellectual Property and Regulatory Affairs. We are serving 55+ markets including USA, Canada, Europe, China, LATAM, ASEAN and all Emerging Markets with innovative and generic products ranging from Active pharmaceutical ingredients (API), Oral formulations, Parenteral (Injectables, Opthalmics) & Other dosagesOur product development efforts drive a portfolio of more than 1,000 products Enabled by our robust R&D team consisting of more 200 scientists and functional experts and more than 150 doctorates, we have filed 1,071 patents and also published over 1,000 papers for peer review over the years.Benefits OfferedAt Dr. Reddys we actively help to catalyse 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. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and were 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/#!/,
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Project Management, Communication, Presentation, Formulation, Regulatory compliance,Research Development, Beverages, Ingredients, Processing techniques, Sensory analysis, Product labelling
Regulatory Compliance, Stability Testing, Product Development, Communication Skills,Color Cosmetics, Shade Matching, ProblemSolving, Good Manufacturing Practices GMP
Communication, Interpersonal skills,Problemsolving, Good Manufacturing Practices GMP
Quality Systems, SOPs, Technical Reports, Technology Transfer, Communication Skills, Presentation Skills,Oral Solids, Softgels, Pharmaceutical Excipients, Tablet Compression Machines, Fluidized Bed Processors, Roller Compactors, Softgel Encapsulation Machines, Bioavailability Enhancement, Formulation Techniques
Project Management, Communication, Presentation, Formulation, Regulatory compliance,Research Development, Beverages, Ingredients, Processing techniques, Sensory analysis, Product labelling
Regulatory Compliance, Stability Testing, Product Development, Communication Skills,Color Cosmetics, Shade Matching, ProblemSolving, Good Manufacturing Practices GMP
Communication, Interpersonal skills,Problemsolving, Good Manufacturing Practices GMP
Quality Systems, SOPs, Technical Reports, Technology Transfer, Communication Skills, Presentation Skills,Oral Solids, Softgels, Pharmaceutical Excipients, Tablet Compression Machines, Fluidized Bed Processors, Roller Compactors, Softgel Encapsulation Machines, Bioavailability Enhancement, Formulation Techniques