Nysa Biomed Pvt. Ltd.

Role & responsibilities Develop and optimize formulations for various dosage forms (tablets, liquid orals, ointments, etc.). Conduct R&D activities to create innovative and patient-friendly drug products. Perform stability studies to evaluate product quality and shelf life. Analyze and interpret data generated from development and stability studies. Prepare development records, experimental protocols, batch manufacturing documents, stability reports, etc. Collaborate closely with QA, QC, Production, and Packaging teams for scale-up and process validation. Ensure all formulation activities comply with regulatory guidelines and industry standards. Maintain accurate documentation of processes, trials, and observations. Preferred candidate profile Masters / Bachelors degree in Pharmacy, Pharmaceutical Chemistry, or an equivalent field. 5–10 years of relevant experience in pharmaceutical formulation development. Strong technical knowledge of formulation science, pre-formulation studies, stability protocols, and process development. Hands-on experience with solid oral and/or liquid oral dosage forms. Good understanding of GMP, ICH guidelines, and regulatory requirements. Strong analytical, problem-solving, and communication skills. Ability to work independently as well as in cross-functional teams.