Company DescriptionDr. 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 transparencyDr 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 SummaryWe are seeking a visionary and highly experienced Tech Lead - Inhalation to spearhead inhalation product development and technology transfer initiatives. This role includes overseeing end-to-end formulation development, process optimization, and scale-up strategies for inhalation products (e.g., Dry Powder Inhalers (DPIs), Metered Dose Inhalers (MDIs), nebulizers) alongside executing due diligence, gap analysis, project management, regulatory filing, and CMO collaborations to ensure seamless product launches in China, Russia, and other global markets.Roles & ResponsibilitiesProduct Development:Lead inhalation product formulation development, including designing and optimizing formulations for inhalation systems.Pre-formulation studies, prototype development, and compatibility testing with inhalation devices.Drive process development to ensure scalability and compliance with global regulatory standards.Conduct stability studies and analyze product performance to refine formulations for targeted therapeutic outcomes.Technology Transfer:Coordinate technology transfer activities, including scope definition, process alignment, and documentation preparation for seamless integration with CMOs.Ensure alignment of formulation processes with CMO capabilities and regulatory requirements.Due Diligence:Assess composition, Critical Quality Attributes (CQA), Critical Process Parameters (CPP), and Quality Target Product Profile (QTTP) to ensure formulation and process readiness for tech transfer.Perform gap analysis for inhalation products, comparing innovator specifications and market requirements in China and Russia.Regulatory Compliance:Collaborate with regulatory teams to ensure inhalation products comply with pharmacopeia standards in China and Russia.Prepare technical documents for regulatory submissions and address scientific queries from agencies such as CFDA/CDE.Project Management:Develop and track project timelines, ensuring alignment between internal teams and CMOs.Oversee facility setup, equipment qualification, and scale-up strategies for manufacturing inhalation formulations.Validation & Execution:Plan and monitor machine trials, packing material suitability, plant qualifications, media fills, and stability loading for inhalation products.Review and approve process validation protocols, reports, and supporting data.QualificationsEducational qualification: M.PharmaMinimum work experience: 10 years in Formulation Research & Development.Skills & attributes:
Technical Skills
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