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Karnataka

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Clinical research courses

  • Merck Limited looking for Safety Medical Writer, Ph.D, M.Pharm, Pharm.D Apply

    Merck Limited (formerly E. Merck Limited) was set up in India as the first Merck subsidiary in Asia in 1967.  The Company operates both its Pharmaceuticals and Chemicals businesses in the country. Merck was also the first Merck Group Company to go public in the year 1981. The Merck Group now holds 51% of the share capital in Merck Limited, while the remaining 49% is traded on the Bombay Stock Exchange Ltd.

    Post : Safety Medical Writer

  • Walk in Drive for M.Pharm, B.Pharm, M.Sc in Regulatory Affairs Department at Hetero Drugs

    Hetero Drugs is an Indian pharmaceutical company and the world’s largest producer of anti-retroviral drugs. Hetero’s business includes APIs, generics, biosimilars, custom pharmaceutical services, and branded generics. Globally renowned, vertically integrated pharmaceutical player engaged in Research and Development (R&D), manufacturing, and marketing of high-quality chemical and biologic medicines across diverse therapeutic areas.

    Openings for Regulatory Affairs

  • Teva looking for Quality Specialist
    Serve as a Subject Matter Expert on all In-Take Team complaint processes and scenarios and assists QAS employees to ensure compliance with Quality Assurance Services Standard Operating Procedures and Work Instructions
  • Apotex Inc looking for Lead Research Scientist

    Apotex Inc. is a proudly Canadian, global pharmaceutical company that produces high-quality, affordable medicines for patients around the world. Apotex employs almost 8,000 people worldwide in manufacturing, R&D, and commercial operations.  Apotex Inc. exports to more than 100 countries and territories and operates in more than 45 countries, with a significant presence in Canada, the US, Mexico, and India.

  • Novo Nordisk Require Medical Writing Specialist
    Communicate clinical data clearly and concisely, contributing to process improvements, knowledge sharing, and skill building. Mentor and train other medical writers as needed, while maintaining good relationships with stakeholders and colleagues.
  • Eurofins Scientific Hiring Manager, Sr. Manager, AGM Business Development
    Skill on lead generation and tapping new business opportunities from innovators. Extensive exposure to Business Development, Budgeting and Business Planning.
  • Opportunity for M.Pharm, B.Pharm, MSc to Join Novo Nordisk as Regulatory Professional
    As Regulatory Professional II, the candidate will be responsible for making the timely submissions to the Health Authorities worldwide.
  • Job for M.Pharm, MSc as Research Associate, Executive at Micro Labs Limited
    Having good experience of method development on HPLC and GC instruments and other analytical instruments. Having knowledge of wet analysis
  • Work as Regulatory Specialist MSR Coordination at GSK India
    With minimal input from manager, manages multiple project assignments supporting Variations, Product Expansion dossiers, Renewals and regional projects simultaneously; MSR packages/documents will range in complexity
  • IQVIA Hiring Safety Associate Trainee
    Review, assess and process Safety data and information, across service lines, received from various sources and distribute reports/data onwards to both internal and external third parties following applicable regulations SOPs and internal guidelines under guidance and support of senior operation team members.
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