Minimum Bachelors degree in Life Sciences or Pharmaceutical Sciences required. Masters / other advanced degree or MBA in business administration or a scientific field preferred.
Senior Process Development Scientist based in Bangalore, India, to join our team of scientists and engineers within the company dedicated to supporting our technologies in the biopharmaceutical industry for production of biotherapeutics including advanced therapy modalities.
Addressing the question of whether and how immune cells in the central nervous system traffic out, researchers have now identified a perineural pathway through which the HIV virus can redistribute throughout the body.
An international clinical study led by the Medical University of Vienna shows that the drug patritumab deruxtecan (HER3-DXd) can have a promising effect in patients with active brain metastases of various tumour types.
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.
Performs testing not only of raw materials and drug products, maintenance and calibration of analytical instruments, prepares standard and sample solutions and maintains appropriate records. Carry out checks of record documentation.
Assist in conducting and reporting audits for Sun Pharma sites associate with Pharmacovigilance activities/ operations to assure adequacy & adherence with established Quality Systems.
Develop stability study designs for new product development and sustaining product projects. Contribute to technical feasibility analysis of complex research and design concepts. Evaluate results relative to product requirements, definitions and/or program goals.