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Job description

Role & responsibilities • Formulation Development for oral solid dosage form including tablets, capsules and oral liquids • Execute development, scale-up and exhibit batch activities • Optimize formulations for stability, bioavailability and manufacturability • Develop QbD based formulation strategies and support regulatory documentation • Respond to regulatory queries for global market • Cost efficient API and excipient implementation • In-dept understanding of SOD design and optimization • Strong knowledge of QbD, DOE and process close-up • Experience with regulatory guidelines(FDA, EMA, HC & ICH) • Excellent problem solving, documentation and communication skills • Collaborate with analytical QA, PDL and regulatory teams to ensure successful product development technology transfer • Good exposure to IR, ER, DR, MR, SR Formulations

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