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Clinical courses

 

Clinical research courses

  • Applications are invited post of Research Scientist at NITVAR

    M.Sc, Ph.D in life sciences with at least 2 year experience in research laboratory with hands on Immunological and Molecular Biology techniques, handling infectious agents and data management. 
  • Torrent Pharma Walk in Drive for M.Pharm, B.Pharm, M.Sc in QA and QC Formulation, Formulation Technology Transfer
    Experience in Documentation, Issuance, CCF, Trackwise, SOP preparation, well versed with GMP and Regulatory requirements of USFDA, EU, ANVISA, AQA.
  • Interview for M.Pharm, B.Pharm, M.Sc in Manufacturing at Amneal Pharma

    Amneal is a global essential medicines company powered by a robust U.S. generics business. Amneal is a growing branded business with deepening portfolios in institutional injectables, biosimilars and select international markets including India.

    Looking for candidates with relevant experience in injectable regulated plant as mentioned below

  • Walk in interview for B.Pharm Apprentices at NMDC Limited
    Candidates applying for A Trade ITI Apprentices mentioned in the above table must possess ITI Trade Qualification Certificate from an institution which is recognized by National Council of Vocational Training NCVT / State Council of Vocational Training SCVT. 
  • Job for M.Pharm, B.Pharm, MSc in QA, QC at Virchow Biotech

    VBPL is an ISO 13485:2012 and WHO – GMP certified leading global player in Biopharma sector having more than 15 years of operational experience, situated at Hyderabad. We also have offices located in USA. Innovative, ever motivated Research team and uncompromising manufacturing team in providing quality products are our strengths.

  • Interview for B.Pharm, MSc in Production, Quality at Glenmark Pharmaceuticals
    The applicant must have experience in pharma units approved by regulatory agencies like USFDA, MHRA etc.
  • Work as Senior Research Associate at Piramal Pharma Solutions
    Preparation of technical documents like development reports, manufacturing docs, technology transfer documents. Ensuring good documentation practices.
  • Work as Clinical Data Svs Associate at Accenture - B.Pharm, M.Pharm Apply

    Accenture is a global professional services company with leading capabilities in digital, cloud and security. Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song all powered by the world’s largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries.

  • Work as Senior Regulatory Writer at Novartis
    Lead Writer for simple submissions, contributing to key messaging and pooling strategy, providing content guidance, and ensuring compliance of documentation to internal company standards and external regulatory guidelines.
  • Sanofi Hiring Signal Manager
    Risk-based monitoring is an adaptive approach to clinical trial monitoring that directs focus and activities to critical data and processes that have the most potential to impact patient safety and data quality.
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