Applications are invited for the post of Director at National Institute of Biologicals
National Institute of Biologicals (NIB) had been set up in 1992 as an apex autonomous Institute under the administrative control of the Ministry of Health & Family Welfare, Government of India for promoting and protecting human health through various activities assigned to it. The mandate of the Institute includes ensuring provision of quality biological drugs i.e Invitro diagnostics, Vaccines and Biotherapeutics, including therapeutic monoclonal antibodies used by patients suffering from cancer and autoimmune diseases by undertaking high end science based testing with R&D interface for application of science.
Post : Director
The Government of India has set up the National Institute of Biologicals, an autonomous institution under the Ministry of Health & Family Welfare, Government of India which is a premier scientific institution and a centre of excellence to ensure quality of vaccines and biologicals in the country. The Institute is looking for a competent, dedicated and dynamic person for the post of Director as per details below.
Scale of pay : Revised Pay Matrix Level- 15, Rs.1,82,200-2,24,100/-plus NPA as applicable for Medical personnel as per rules.
Method of Recruitment : Direct Recruitment through a Search -Cum-Selection Committee.
Age : Not Exceeding 56 years.
(A) Medical: - PG Medical degree in the field of Microbiology / Biochemistry / Immunohaematology & Blood Transfusion / Pharmacology from a recognized University
Ph. D in the above mentioned fields.
(B) Non-Medical: (i) M. Sc in Microbiology / Clinical Microbiology / Biotechnology/ Bioinformatics / Biochemistry from any recognized University with at least 60% marks and
(ii) Ph. D in the above mentioned fields.
(i) 20 years in the profession with experience in any of the following areas:
a) Research in Biologicals and Biotherapeutics, Quality Control Testing of Biologicals and Biotherapeutics;
b) Review of Technical Dossiers of Biologicals and Biotherapeutics including Vaccines in respect of Chemistry Manufacturing Control (CMC), non-clinical trial data on Animal Pharmacology/ Animal Toxicology, Clinical Trial data;
c) Review of Technical Dossiers of 'In Vitro Diagnostic (IVD) Medical Devices' in respect of conformation to the Essential Principles of Safety and Performance of Medical Devices which include Product Description, Design and Manufacturing information, Product performance specifications and associated validation and verification studies, Labelling and Regulatory history;
d) Evaluation & Review of Adverse Events:
i) following Immunization (AEFI)
ii) associated with Biologicals and Biotherapeutics (Pharmacovigilance)
iii) associated with blood transfusion and blood products administration (Haemovigilance);
iv) due to indirect harm associated with IVD Medical Devices (Materiovigilance)
e) Management of Quality System with application of ISO : 17025 and ISO : 34 with Total Quality Management approach for at least 15 years after acquiring Ph.D
(ii) At least 3 years administrative experience.
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