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.
Teva Pharmaceuticals USA, Inc., and affiliated companies have agreed to pay USD 35 million to resolve a class action lawsuit alleging that the drugmaker delayed generic competition for its asthma inhaler, QVAR
Postgraduate degree in Science/ Pharmacology/ Life Sciences/ Regulatory Science/ Public Health from a recognised University with atleast 6 years of relevant work experience
BRIC-Institute of Life Sciences (ILS), Bhubaneswar, an autonomous Institute of the Department of Biotechnology, Ministry of Science & Technology, Government of India, engaged in advanced research, invites applications from Indian nationals
Post Graduate degree in Biological Sciences / Post Graduate Degree in a professional Course from a recognized University or equivalent; and the candidates should have cleared any National Level Eligibility test such as (NET / GATE etc.).
Masters Degree from a recognized University or institute in any of the disciplines specified in Pharma, Life Sciences, Biotechnology. Experience in Research and Development in Industry or Academic Institution or Science and Technology Organization.
55% marks in B.Sc / M.Sc. (Bioscience/ Life Sciences). Experience Preference will be given to candidates possessing knowledge or experience in Microsoft Excel.
PhD in Biotechnology, Microbiology, Nanobiotechnology, Bioengineering, Nanotechnology, any other related interdisciplinary engineering and / or science.
Ability to understand and analyses the complex data and performs the activities including accessing the case in Argus, code and enter data. Be fully competent to perform all steps within the case-handling processing.
Hetero is one of worlds leading producers of key Active Pharmaceutical Ingredients and generic formulations with presence in 140+ countries and backed by 30 years of experience in the pharma sector.