Control manufacturing activities in the respective section to ensure activities carried out are as per requirement of cGMP & safety to meet the quality and manufacturing targets in time
Exposure of analysis for Finished Products, Stability Samples & Raw Materials. Having Knowledge of Analytical Method Validation, Verification & Method Transfer. Having skill for data interpretation, troubleshooting. Pharma knowledge of Solid orals & Quality process.
Openings in R&D, AR&D, Production, Labelling & Packing at Hetero Biopharma. Process development & scale-up. Tech transfer experience. DoE / QbD based process studies
BSc - Chemistry/ B Pharma/ Diploma / ITI / 12th with Science Background. Upon successful completion of the training, selected candidates will be absorbed at various Ipca Laboratories locations as per compatibility and skills
B.Pharm or D.Pharm from a recognized university, the operationalization of the BHISHM, Bharat Health Initiative for Sahyog, Hita and Maitri Cube Project funded by the Disaster Management cell, under the Ministry of Health and Family Welfare, Government of India at AIIMS
Master of Science, M.Sc. in Chemistry / Analytical Chemistry or Master of Pharmaceutical Sciences M.Pharma in Chemistry / Analytical Chemistry from a recognized University / Institution. Central Ayurveda Research Institute, CARI Bengaluru
M.Pharm. / M.V.Sc. / M. Tech. Biotechnology or M.Sc. Biotechnology/ Biochemistry / Microbiology or equivalent. Regional Ayurveda Research Institute under the aegis of Central Council for Research in Ayurvedic Sciences, Ministry of AYUSH, Government of India
Post Graduate in Pharmacology M.Pharm / M.S Pharm, Post Graduate, M.Sc. in Biomedical Sciences, Life Sciences, Physiology, Biochemistry & Biotechnology, Investigating the role of sodium modulation in enhancing Lenvatinib sensitivity and overcoming Lenvatinib resistance in Hepatocellular Carcinoma Cells