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  • 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
    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
    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
    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
    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
    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
  • Teva Hiring Clinical Research Associate - M.Pharm, B.Pharm, MSc Apply
    Teva Hiring Clinical Research Associate - M.Pharm, B.Pharm, MSc Apply
    Maintaining detailed records of studies as per FDA and other required guidelines, including things such as drug administration and subject specific case report forms.
  • iBRIC-inStem invites applications for Postdoctoral Fellow
    iBRIC-inStem invites applications for Postdoctoral Fellow
    Doctoral Degree in Science from a recognized 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.
  • Remote jobs in regulatory affairs at PAREXEL
    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)

  • Walk in Drive for B.Pharm, BSc in Production, Packing at Hetero Drugs
    Walk in Drive for B.Pharm, BSc in Production, Packing at Hetero Drugs
    Hetero Drugs is an Indian pharmaceutical company and the worlds largest producer of anti-retroviral drugs. Hetero business includes APIs, generics, biosimilars, custom pharmaceutical services, and branded generics.
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