master file , Validation Master Plan, Calibration planner, Validation protocol, reports , stability testing protocol , specification etc. Experience: 15-20 Years Relevant Experience: Candidate from Pharmaceutical(Injectable) having good exposure of GMP environment with relevant exp of 15-20 Years
Sterility testing of finished products by membrane filtration method and Direct Inoculation. .. Calibration of equipment such as pH meter, Balance, Conductivity meter etc. Media preparation, Autoclave loads and Growth promotion test for all prepared Media. Sampling of sterile finish product. Sampling
With Knowledge of Chemical Analysis, Instrument Analysis/handling viz. HPLC / GC / FT / IR, Calibration of Equipments, RM / PM/ Bulk / Finished Product Testing, Sampling, Stability, Method Validation, preparation of STP, SOP, etc. and Ready to work in shifts ...
and installed stability chambers. Responsible for maintenance management of utility and production equipments, purified water system. Develop, implement and maintain energy conservation programs. Maintenance of tools and spare parts. Vendor development and management of contract maintenance. Maintenance
Implement company strategy 6. Make availability of company products 7. Achieving sales target Qualification: Any graduate(preferred Bsc/BPharma) Age:22-29 years of experience (For ME / MR) Experience: Min 1 year in pharma sales CTC best in the industry+Incentives+Allowances