Karnataka

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  • Remote jobs in regulatory affairs at PAREXEL
    1 October 2024

    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)

  • 30 September 2024
    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.
  • 30 September 2024
    Syngene Hiring Assay Biologist | MSc or MTech in Life sciences Apply
    The ideal candidate will ensure smooth running of multiple cell-based and biochemical assays while maintaining highest quality and integrity of data and meeting established timelines.
  • 30 September 2024
    Require Regulatory Project Manager at Merck
    Works closely with the Global Regulatory Lead, Regulatory Affairs Manager providing the submission strategy and with the Submission Manager executing the submissions.
  • 30 September 2024
    AstraZeneca looking for Clinical Coder
    In this role, you will perform coding activities on the assigned project in a timely and efficient manner, code the Medical Conditions and Medication terms in the Coding tool, generate Queries to clarify in order to facilitate coding, and participate in study related meetings as needed.
  • 28 September 2024
    Job for Pharmacy graduates as Technical Assistant at NITM - Pay Matrix Rs. 35,400-1,12,400
    First class bachelor degree in Pharmacy, relevant subject Pharmacology from a recognized university in relevant field.
  • 27 September 2024
    Require SERM Scientific Director at GSK
    Leads Pharmacovigilance and Risk Management Planning and develops strategy for approach to evaluation of issues in the clinical matrix. Leads the safety component of global regulatory submissions.
  • 26 September 2024
    Quality Medical Reviewer Require at Lilly
    The purpose of the Quality Medical Reviewer role in Medical Affairs is to review and approve medical and promotional materials to ensure they are medically accurate and interpreted correctly based on the review of references, citations and data available.
  • 25 September 2024
    Opportunity for Ph.D or M.Pharm, MSc as Research Scientist at SJRI - Salary Rs. 85,000 pm
    Post graduate Degree or PhD in Life Sciences, Pharmacology and Biomedical engineering with experience three years in conducting large scale intervention studies.
  • 25 September 2024
    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.
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