+ M. Pharm with good exxperience inFormulation Research and development Experience of Peptides Injectables dosage form with Experience in Drug Device Combination Products. + Execution of Various Pre-Formulation, Compatibility, Hold Time & Stability Studies. + Experience in technology transfer activities to plants Scale-up & Exhibit batches Troubleshooting & Technology transfer Documentation i.e. Master Formula Record, Stability Protocol & Development Protocol & Reports. + Preparation of Regulatory Filling Documents (Strategy document, Product Development Report, Nitrosamine, Elemental & Extractable Risk Assessment reports etc.) for advance regulated market of Peptides products + Understanding about regulatory requirements of Peptides Injectables dosage form i.e FDA, EU, Canada, Brazil. Russia & Australia We provide equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, military or veteran status, generic predisposing characteristics or any other basis prohibited by law.