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  • Work as Regulatory Professional at Novo Nordisk - Ph.D, M.Pharm, MSc Apply

    You will be a member of a newly established virtual team - EU Submission Hub with colleagues in Denmark, Portugal, Poland and Bangalore focusing on clinical trial submissions in EU. EU Submission Hub is part of Submission Management department, who is responsible for electronic submissions to Health Authorities including New Drug Applications and Life Cycle submissions.
  • Work as Quality Control Associate / Senior Associate at Stelis Biopharma
    Preparation of quality system related, Instrument operation related SOPs, Specification, STPs, GTPs, raw data sheet, certificate of analysis. Preparation, review, execution of method transfer and method validation protocols and reports etc.
  • Job for Assistant Professor at Manipal College of Pharmaceutical Science

    Manipal Academy of Higher Education is a globally engaged institution with active partnership with more than 220 leading universities around the globe. Our relations with institutions, government agencies and organisations in study, research and service provide faculty and students access to world-class institutions, experiences and resources. 

  • Require Regulatory Professional at Novo Nordisk
    As Regulatory Professional II, the candidate will be responsible for making the timely submissions to the Health Authorities worldwide. The candidate is expected to establish and maintain the CMC part of the core regulatory file. 
  • Opportunity for M.Pharm or MSc, MTech to work in DST sponsored project at JNCASR
    Candidates with laboratory experience in human cell culture, animal handling and prior knowledge of developing therapeutics for different infectious and non-communicable diseases will be preferred 
  • AstraZeneca Hiring Associate Director - Clinical Regulatory Writing

    AstraZeneca contributes meaningfully to the UK beyond the provision of our medicines and the benefits they provide to the health of the nation. We commissioned a report in 2009 to measure our significant investment to the UK economy, which includes investment in jobs and wealth creation. Oxera, an independent economic consultancy provided the analysis for this report.

    Post : Associate Director, Clinical Regulatory Writing

  • Walk in Drive for M.Pharm, B.Pharm, M.Sc in Regulatory Affairs Department at Biocon

    Biocon is global biopharmaceutical company changing patients' lives in over 120 countries by finding new and affordable ways to treat diabetes, cancer and autoimmune diseases. Biocon is a research-driven, global healthcare company with a strong matrix of capabilities along the biopharmaceutical value chain.

    Department : Regulatory Affairs

    Experience : 3-12 years
    Qualification : M.Pharma / M.Sc / B.Pharma
    Job Location : Bangalore

  • Life Sciences Recruitment at Centre for Cellular and Molecular Platforms
    The Drosophila Facility at the CCAMP has an opening for Facility Assistant. The job responsibilities for the position include Maintenance of Drosophila stocks. Molecular and phenotype-based screening of mutant and transgenic Drosophila stocks. Generation of transgenic flies Fly husbandry and genetics.
  • AbbVie looking for Product Manager
    Support implementation of Marketing-led initiatives including supporting coordination with partner agencies to deliver appropriate campaign content, logistic support for cycle and kick-off meetings, patient-focused solutions and multi-channel and digital campaigns.
  • Interview for JRF, Project Associate, Lab/Field Assistant at CIMAP

    CSIR-Central Institute of Medicinal and Aromatic Plants (CSIR-CIMAP) is a premier multidisciplinary research institute of Council of Scientific and Industrial Research (CSIR), India with its major focus on exploiting the potential of medicinal and aromatic plants (MAPs) by cultivation, bioprospection, chemical characterization, extraction, and formulation of bioactive phytomolecules.

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