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  • CSIR-CIMAP interview for Project Associate post

    M.Sc. in Biotechnology, Biochemistry, Microbiology, M.Tech in Biotechnology from a recognised University. Working experience in Biotechnology, Molecular Biology, yeast biology.
  • Job as Principal Medical Writer at PAREXEL
    Principal Medical Writer, will research, create, and edit all documents associated with clinical research. The Principal Medical Writer may operate as the project lead writer, submission coordinator and primary client contact to manage contributions of multiple writers working on related documents.
  • Baxter looking for Nitrosamine professionals to join R&D team

    Baxter provides a broad portfolio of essential renal and hospital products, including home, acute and in-centre dialysis; sterile IV solutions; infusion systems and devices; parenteral nutrition; surgery products and anesthetics; and pharmacy automation, software and services. The company’s global footprint and the critical nature of its products and services play a key role in expanding access to healthcare in emerging and developed countries. 

  • PAREXEL Hiring Regulatory Affairs Consultant, Associate, Senior Associate
    Contribute to preparation including authoring where relevant and delivery of simple, and with experience, increasingly more complex regulatory maintenance submissions from either a global and, or regional perspective.
  • 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.
  • Remote jobs in regulatory affairs at PAREXEL

    PAREXEL has supported the Bio-Tech and Pharmaceutical industries in helping the development of new drugs and treatments on a global basis. As a leading global biopharmaceutical service provider, they supply knowledge-based contract research, medical communications and consulting services across a broad range of therapeutic areas to the worldwide pharmaceutical, biotechnology and medical device industries.

    Post : Senior Regulatory Affairs Associate (Labelling)

  • Stelis Biopharma Hiring Management Trainee
    Market research and analysis of CDMO landscape, Biologics, Biosimilars and Small Molecules business. Refer databases, news, articles etc and generate leads for potential business, newer technologies etc. Reach out to leads and present about One Source Capabilities.
  • Invites online applications for the post of Scientific Officer at NCBS - Permanent Job for Life Sciences candidates
    Ph.D. in Biotechnology, Life Sciences, chemistry, physics from a recognized University, Institute. Minimum Two years post-doctoral experience in Microscopy or Flow Cytometry. 
  • Pharma and Life Sciences Recruitment at National Centre for Biological Sciences
    M.Pharma, Masters in any biological sciences and life sciences with prior experience in handling laboratory mice or rats with experience in molecular biology techniques is desirable. Experience in molecular biology techniques such as PCR, DNA/RNA extraction, gel electrophoresis, genotyping
  • Opportunity for Life Sciences candidates to Join NCBS as Grants Adviser
    MSc in Life Sciences. Minimum 2 years experience in the relevant field viz., grants management/research management etc., Proven communication skills
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