Assistant Manager, Sr. Executive

Job description Role & responsibilities Conduct pre-formulation and formulation development of new pharmaceutical dosage forms (solid, liquid, semisolid, etc.). Perform compatibility studies for Drug-Excipient interactions. Design and execute laboratory-scale and pilot-scale trials. Develop and optimize manufacturing processes, ensuring scalability and reproducibility. Maintain batch manufacturing records (BMRs) and development reports. Support analytical development teams with stability and validation studies. Assist in technology transfer to production and contract manufacturing sites. Ensure adherence to GMP, GLP, and regulatory guidelines (e.g., USFDA, MHRA, WHO). Collaborate with cross-functional teams: QA, QC, Regulatory Affairs, and Production. Troubleshoot formulation and process-related issues. Participate in product lifecycle management and cost optimization initiatives. Preferred candidate profile Strong knowledge of formulation principles and pharmaceutical excipients. Experience in process optimization and scale-up. Familiarity with equipment like granulators, tablet presses, blenders, etc. Attention to detail and documentation accuracy. Good communication, problem-solving, and team collaboration skills. Role: Research & Development - Other Industry Type: Pharmaceutical & Life Sciences Department: Research & Development Employment Type: Full Time, Permanent Role Category: Research & Development - Other Education UG: B.Pharma in Any Specialization PG: M.Pharma in Any Specialization Key Skills Formulation & Development