Ipca is a fully integrated, rapidly growing Indian pharmaceutical company with a strong thrust on export. Ipca'a API and Formulation produced at world class manufacturing facilities are approved by leading drug regulatory authorised including the USFDA.
Post : Manager - Quality Assurance (QMS & Documentation Lead)
M.Pharm / Ph.D ; Candidates having 3 to 8 years experience in Product development of Solid Orals, Onco OSD, Liquid Orals and Sterile formulations. Markets handled : Regulated / ROW / Domestic.
Responsible for monitoring and ensuring quality of products and comply with cGMP standards. Monitoring of critical process parameters, line clearance before batch initiation, verification of RM and equipment. In process sampling for quality check like pH, moisture content, and reaction monitoring.
To Review Qualification Protocol and Reports of Equipment, Instrument, System.To Review Qualification Protocol and Reports of Computer System Validation CSV. Ensuring safe handling of Raw Materials and Packing Materials. Dispensing activity of RM and PM material.
Supervision of Micro Section Microbiological Analysis of Raw Material, Finished Product, Water Samples, Stability ad Hold Time study Samples. Review and Verification of Micro documents, Preparation of Protocols and SOP, QMS, Environment Monitoring Media Preparation, GPT Test, Microbial, Limit Test of Finished Product and Raw Material, Water Testing etc. - Calibration and Validation of Microbiological Instruments.
Minimum 1-3 years of relevant experience in operation and supervision of Compression, Granulation & Coating m/c i.e Fette, Glatt,Ganson,Imprinting etc.