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academics

 

Clinical research courses

  • Novo Nordisk looking for Senior Regulatory Professional

    As Regulatory Professional, the candidate will be responsible for making the timely submissions to the Health Authorities worldwide. The candidate is expected to establish and maintain the CMC part of the core regulatory file. Further responsibilities include Life Cycle Management.
  • Require Quality Manager at Novartis - B.Pharm, M.Pharm Apply
    Bachelor, Masters Degree with experience in Pharmaceutical Industry; Acts as a single point of responsibility for application for ensuring the system and data are secured as required by Information Security and Compliance requirements.
  • Emcure Inviting applications for Regulatory Affairs

    Emcure is fast-growing Indian pharmaceutical company engaged in developing, manufacturing, and marketing a broad range of pharmaceutical products globally. With a presence in over 70 countries, Emcure's goal is to constantly innovate and deliver affordable & high-quality healthcare solutions to people.

    Post : Regulatory Affairs

  • Work as Senior Manager at Sun Pharmaceutical - M.Pharm, B.Pharm, MSc Apply
    To author and review quality agreements between Sun Pharma & CMO site. Also, ensure qualified and approved external service providers are used.
  • Exelixis looking for Associate Trial Master File Director
    Clearly and proactively anticipates, identifies, tracks, communicates, and proposes solutions for discrepancies in priorities and plans, prioritize complex and multiple/conflicting responsibilities and/or issues.
  • Johnson & Johnson is recruiting for Director, Clinical Trial Project Management - Immunology

    At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.

  • Novartis looking for Principal Scientific Writer - M.Pharm, MSc Apply

    Novartis has one of the most exciting product pipelines in the industry today. A pipeline of innovative medicines brought to life by diverse, talented and performance driven people. All of which makes them one of the most rewarding employers in their field.

    Post : Principal Scientific Writer

  • Require Regulatory Affairs Manager at Sun Pharmaceutical
    Monitoring for Documents compilation activities for New product filing , Re-Registration, renewals from plant dossier filing , sample requirements etc. Participation in Action plan discussion for queries from different Regulatory agencies and monitoring for submission of data, documents from plant.
  • Teva looking for Senior Manager Regulatory Affairs - M.Pharm, B.Pharm, MSc Apply

    Teva is a global pharmaceutical leader and the world's largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide.

    Post : Sr Mgr Regulatory Affairs

  • Opening for QMS Manager at Torrent Pharma, M.Pharm, MSc Apply

    Torrent Pharma, the flagship Company of Torrent Group is one of the leading pharma companies of the Country. The Company was a pioneer in initiating the concept of niche marketing in India and today is ranked amongst the leaders in therapeutic segment of cardiovascular (CV), central nervous system (CNS), gastro-intestinal (GI) and women healthcare (WHC). The Company also has significant presence in diabetology, pain management, gynaecology, oncology and anti-infective segments.

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