Job Description

Job Responsibilities: Perform pre-formulation studies, R&D trials and support scale-up activities. Conduct R&D trials for oral solid dosage forms (tablets, capsules, etc.). Develop and optimize formulations to meet regulatory and quality requirements. Document and analyze trial data to improve formulations. Collaborate with cross-functional teams for technology transfer to manufacturing. Requirements: M.Pharm or equivalent in Pharmaceutics/Pharmaceutical Sciences. Hands-on experience in formulation development of oral solid dosage forms. Knowledge of QbD, regulatory guidelines, and process optimization. Strong analytical and problem-solving skills.