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  • MedForage : The CADD HACKATHON

    The CADD Hackathon, organized by the Department of Pharmaceutical Chemistry, Faculty of Pharmacy, M. S. Ramaiah University of Applied Sciences. This event will bring together the brightest minds in technology and pharmaceutical sciences for an epic drug discovery dockathon.
  • Opening for Research Assistant at TIGS
    The selected candidate is expected to support in nutritional quantification of rice and other grains. Experience of working with HPLC, UPLC is an added advantage for one of the positions.
  • Job for M.Pharm, B.Pharm, MSc as Pharmacovigilance Manager at Clarivate
    Bachelors degree, Masters Degree in pharmacy, Life Sciences, Nursing, or related field. Advanced degree e.g., PharmD, MD, PhD preferred.
  • Work as Clinical Surveillance Scientist at Lilly
    Advanced medical related graduate degree, such as: pharmacy, nursing with advanced clinical specialty Clinical Nurse Specialist, Nurse Practitioner, PhD with 1-3 years experience in related scientific field.
  • Work as Regulatory Affairs Manager Specialist at Merck
    The Specialist, Regulatory Affairs Manager prepare dossiers and execute actions that support the license security and product compliance on the markets, and that meet companys and health authorities’ requirements.
  • Require Clinical Data Analyst at PAREXEL
    Clinical Data Analyst works under guidance and supervision of their Line Manager and/or Subject Matter Experts to perform some of the clinical data cleaning activities on assigned projects, commensurate with experience and, or project role.
  • Job for Life Sciences candidates at National Centre for Biological Sciences
    Post-graduate degree in Life Science from a recognized university. Proven and excellent written and verbal communication skills in English, with proven ability to write different types of content for a diverse audience. 
  • Lilly Hiring Regulatory Writing Senior Associate Manager
    Bachelors degree in a scientific, health, communications, technology health related field. Demonstrated experience in technical/ regulatory scientific writing.
  • Advertisement for the post of Post Doctoral Fellow at iBRIC-inStem
    Doctoral Degree in Science from a recognised university or equivalent in Biochemistry, Biotechnology, Stem Cell Biology and Neurobiology, Neuroscienc e with a strong publication record and research experience in Cell Biology, Molecular Biology and Neurobiology.
  • Work as Regulatory Affairs Senior Executive at Apotex Inc | M.Pharm, MSc Apply
    Preparation of original DMF, amendments, Annual reports and Review of adequacy of documents for submission. Compilation, review and submission of various Drug master files for US, EU, TGA, Canada and other markets as per respective regulatory guidelines and checklist
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