M.Pharma from a recognized university or equivalent. M.Sc. Biotechnology / Microbiology from a recognized university or equivalent. Working knowledge in the area of Biotechnology.
Post Graduate Degree, including the integrated PG degrees, with five years’ post qualification experience or PhD plus two years post qualification experience.
Individuals desirous of seeking admission to PhD program at NIAB must have a Masters degree (M. Sc., M. Tech., M. V. Sc. or M.Pharm.) or MBBS or B.Tech. (four-year) degree in any branch of Life Sciences.
M.Sc. in Microbiology / Medical microbiology / Biotechnology with at least 2 years of practical experience in various diagnostic microbiological laboratory techniques.
Degree in life Sciences, Health or Biomedical Sciences Pharmacy, microbiology, Biochemistry, Biotechnology, Biophysics etc., or relevant work experience in Pharmacovigilance.
Dossier and document preparation as per CTD,ACTD and country specific guidelines, Review of dossiers, DMF and Technical documents, Answer query raised from regulatory authority.
GBS TMF Team Lead is responsible for the strategic oversight, coordination, and leadership of the GBS TMF Services, ensuring high standards in Trial Master File management and inspection readiness for all assigned clinical trials.