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  • Pfizer Hiring Director for India Business Operations Partner

    Director, India Business Operations Partner, a primary point of contact & dependable partner from Commercial Ops in delivering range of Commercial ops & CMO services and beyond more efficiently and also critical member of Ex LT for India.
  • Sandoz looking for Quality Operations Associate Manager
    Sandoz looking for Quality Operations Associate Manager

    Sandoz become a standalone organization! As a global market leader in Generics and Biosimilar medicine, Sandoz is stepping forward from a position of strength! Those joining Sandoz in the coming months will help shape the future of the company, it’s growth, innovation, culture and how Sandoz impacts the lives of millions. These will be careers with genuine impact! This is one such role.

    Post : Associate manager - Quality operations (GQS-I)

  • Walk in Drive for M.Pharm, B.Pharm, M.Sc in Pharmacovigilance at Tata Consultancy Services
    Walk in Drive for M.Pharm, B.Pharm, M.Sc in Pharmacovigilance at Tata Consultancy Services
    Ability to understand and analyses the complex data and performs the activities including accessing the case in Argus, code and enter data. Be fully competent to perform all steps within the case-handling processing.
  • Work as Senior Regulatory Affairs Associate at PAREXEL
    Work as Senior Regulatory Affairs Associate at PAREXEL
    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.
  • Walk in Drive for B.Pharm, MSc in QA, QC, Production at Glenmark Pharma
    Walk in Drive for B.Pharm, MSc in QA, QC, Production at Glenmark Pharma
    MDl, lnhalers, Nasal, Manufacturing, Filling and Packing, Dispensing, Dispatch, PassX, QMS
  • EY Consulting Hiring Manager
    EY Consulting Hiring Manager

    As a global leader in assurance, tax, transaction and advisory services, we hire and develop the most passionate people in their field to help build a better working world. This starts with a culture that believes in giving you the training, opportunities and creative freedom. At EY, we don't just focus on who you are now, but who you can become.

  • Opportunity for Ph.D, M.Pharm, Pharm.D to Join National Institute for Research in Reproductive and Child Health
    Opportunity for Ph.D, M.Pharm, Pharm.D to Join National Institute for Research in Reproductive and Child Health

    The mandate of the Institute is to address the reproductive health issues of national and global relevance. The institute was established with an objective to develop novel and efficacious modalities for fertility regulation through research and thereby assist the government in its mission to stem the population boom. In the past four decades, however, the institute has grown beyond the mandate with which it was entrusted at the time of its genesis.

  • NIRRCH Life Sciences, Biotechnology, Bioinformatics Recruitment | Salary Rs. 69,440 pm
    NIRRCH Life Sciences, Biotechnology, Bioinformatics Recruitment | Salary Rs. 69,440 pm
    Establishment of Bioinformatics and Computational Biology for Woman and Child Health funded by Department of Biotechnology. Doctoral Degree in Science or Master’s degree in Engineering or Technology from a recognized University or equivalent
  • Regulatory Affairs Trainee Require at Apotex
    Regulatory Affairs Trainee Require at Apotex
    Perform all the labelling update activities and tracking in systems for record maintenance with respect to New Product Development NPD label creation and Product Life Cycle Management PLCM update for products in USA and Canada market
  • Cipla looking for RA Jr. Team Member
    Cipla looking for RA Jr. Team Member
    Assist in submission of product documents to regulatory authorities in accordance with country specific regulatory requirements to ensure approvals and market launch in stipulated time and support in handling post-approval changes, maintenance, and updation of documents during the products life-cycle. Achieve timely submission of dossier/DMF and deficiency responses to regulatory authority by collation, and compiling documents in order to ensure approvals for launch in stipulated time
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