1. Water system Change over and Third phase study of water system validation2. Presently working in validation/Calibration teama. Dry Heat Sterilizer performance Re qualifications.b. Sterile & Non sterile Equipments Validation.c. Media fill validation.d. Process Validation. e. HVAC/Clean area Validation (HEPA filter integrity, Number of Air changes, air particle count, Air flow Pattern, Differential pressure monitoring, Temperature and RH monitoring and Viable air particle count-Air sampler method, Contact plate method, settle plate method and swab testing ), personnel monitoringf. Area qualification g. Autoclave performance Re qualifications.h. Optical inspection validation(Challenge test)i. Disinfectant validation.j. Hold time study of Sterile Garmentsk. Compressed air testing and its validation.3. In-Process Line clearances of Sterile & non Sterile area.a. Dispensing.b. Manufacturing.c. Dry Powder filling Injection.d. Liquid- Filling Injection. e. Granulation area.f. Compression. g. Coating and Packaging area.h. Verification of weighing balance, Magnehelic gauge, Temperature, and relative humidity of