Academic jobs for M.Pharm/Ph.D as Assistant Professor at NIPER | 09 posts
National lnstitute of Pharmaceutical Education and Research (NIPER)is an autonomous institution established under the aegis of Department of Pharmaceuticals, Ministry of Chemicals and Fertilizers at Hajipur, district Vaishali, Bihar It is being set up as a centre of excellence for higher education, research and development in pharmaceutical sciences under Act of Parliament(NIPER ACT 1998). The Institute is conceived to provide leadership in pharmaceutical sciences and other related areas and admits students for M.S.(Pharm.) Pharmaco-informatics, M.Pharm. Pharmacy Practice and M.S.(Pharm.) Biotechnology to begin with. Subsequently more postgraduate and doctoral programmes courses would be added on the lines of NIPER,SASNagar, Mohali (Punjab). A full-fledged campus is envisaged to set up on 100 acres of land to be allotted by Bihar Government near the present site. It would be the Endeavour of the Government to setup the permanent campus in public-private partnership model to the extent possible.
In terms of Govt. of India, Ministry of Chemicals and Fertilizers, Department of Pharmaceuticals letter No. 57011/1/2010 – NIPER (Vol.II), dated: 24th July, 2017, National Institute of Pharmaceutical Education and Research, Hajipur (NIPER-HAJIPUR) invites application from Indian citizen for engagement of following personnel on contract basis on consolidated pay initially for a period of one year subject to renewal on the basis of performance and mutual consent or till posts are sanctioned, whichever falls earlier.

Agharkar Research Institute (ARI) is an autonomous, grant-in-aid research institute of the Department of Science and Technology (DST), Goverment of India. It was established in 1946 by the Maharashtra Association for the Cultivation of Science as MACS Research Institute and renamed as ARI in 1992 in honour and memory of its founder Director, late Professor S.P. Agharkar.
The U.S. Pharmacopeial Convention (USP) is a scientific nonprofit organization that sets standards for the identity, strength, quality, and purity of medicines, food ingredients, and dietary supplements manufactured, distributed and consumed worldwide. USP’s drug standards are enforceable in the United States by the Food and Drug Administration, and these standards are used in more than 140 countries.
The Central Drugs Standard Control Organization (CDSCO) is the Central Drug Authority for discharging functions assigned to the Central Government under the Drugs and Cosmetics Act. CDSCO has six zonal offices, four sub-zonal offices, 13 port offices and seven laboratories under its control.Regulatory control over the import of drugs, approval of new drugs and clinical trials, meetings of Drugs Consultative Committee (DCC) and Drugs Technical Advisory Board (DTAB), approval of certain licences as Central Licence Approving Authority is exercised by the CDSCO hqrs.

