B.Pharm

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.

B.Pharma Ay with minimum 1 year of professional experience in a reputed institution, hospital; OR  Diploma in Ayurvedic Pharmacy Not less than 02 years duration with minimum 03 years of professional experience in an Institution! Hospital

EM, Media 111 visual inspection , Aseptic area monitoring, Water and Bioburden testing & Sterility testing & BET Testiug , IQ, OQ, PQ of equipment, Biological reactivity test - Moda exposure

Should have sound knowledge of BFS machine operation, aseptic area, maintenance, media fill, batch mfg., CIP, SIP, Autoclave, topical manufacturing. Candidate having experience in different packing lines of OSD & sterile manufacturing.

Fermentation Microbial, mammalian, Proficiency in aseptic technique, exposure to Centrifugation, TFF, Homogenization operation, Filter integrity testing, CGMP, Autoclave operation, media preparation

B.Pharm with minimum 01 year of experience OR D.Pharm with minimum 03 years experience. Experience in Dispensary, Pharmacy of the Hospital having minimum 200 beds. Candidate should be prepared to work in shift duties, including night shift. Registration with State Pharmacy Council with duly allotted Registration Number is mandatory. Experience of working on computerized system desirable.

First-class post-graduate degree included the integrated PG degree OR Second-class post-graduate degree included the integrated PG degree with Ph.D. The Role of Extra Domain A Fibronectin in NETosis-Mediated Non-Ischemic Cardiac Hypertrophy 

Provide strategic guidance and expertise in oncology for the development and execution of medical affairs plans focusing on Lung Cancer, GU Cancers and Hematology portfolio. Collaborate with cross-functional teams to support the successful launch and commercialization of oncology products.

To assist establishing a system in accordance with Good Manufacturing practice guidelines and responsible for follow established , new procedures, new procedures, maintaining and updating existing procedures in the department.