A competent professional in Formulation R&D/Regulatory affairs/Technology Transfer/Project Management. Abilities in synergising operations to facilitate organizational growth & strengthen organization culture through involvements with hard works & self-motivation.My duties & Responsibilities:♦ Literatures/Patents survey♦ Preformulation Studies♦ Lab scale batches♦ Execution of experimental work and documentation under cGMP ♦ Comparative study with the Market Product♦ Stability studies♦ Scale up and technology transfer♦ Preparations of technology transfer documents♦ Process Validation♦ Compliance with cGMP standards/ cGLP Standards♦ Providing necessary support to other teams♦ Communicating to other departments such as QA, QC, Purchase and storesI want to work in an organization where I can prove myself & contribute towards the growth of an organization & that could also boost up my career.Specialties: Strong experience in Preformulation/Clinical/Pre-clinical/Solid oral(IR& MR Tablets, Capsules, MUPS, Pellets, NDDS)/Semisolid(Gels,Cream, Pasteand Ointments)/liquid dosage forms(Syrups, Suspensions, Injectables) development, Scale up from lab scale to commerical scale level with trouble shooting skills