Research Associate - Formulations R&D

You will be responsible for the development of new products and optimization of existing formulas across different product lines such as solid dosage products (tablets, capsules) and other delivery forms (liquids, powders) for regulated markets including the US, Europe, and ROW. Your tasks will involve formulation and process development of oral dosage forms, troubleshooting unresolved formula issues, designing formulation trials, and evaluating stability data to finalize composition. Additionally, you will develop manufacturing processes for R&D formulations to ensure successful technical transfer for large-scale batches. In this role, you will write and review various documents such as master formulas, manufacturing procedures, SOPs, stability protocols/reports, process validation protocols/reports, Product Development Reports, and QOS. Collaboration with other departments like Analytical Method Development, Regulatory Affairs, Quality Control, Quality Assurance, and Inventory Control will be essential to expedite the development and approval of new products by the FDA. Practical experience in development, technology transfer, and ANDA submissions for solid/liquid oral dosage forms (solutions, suspensions, tablets, capsules) for regulated and semi-regulated markets like the US, Europe, and ROW is a key requirement. The ideal candidate for this position should hold a minimum Master's Degree in Pharmaceutical Sciences and possess at least 1 year of relevant experience.,