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  • Novartis looking for Regulatory Writer

    Join Novartis as a Regulatory Writer and contribute to high-quality clinical and safety documents supporting global drug submissions. Ideal for candidates with medical writing experience.
  • Work as Regional Medical Lead at Novartis
    Lead the development and execution of local medical strategies aligned with global and franchise objectives. Identify strategic drivers and shape the patient journey and stakeholder engagement plans.
  • Novartis Hiring R&D Quality Manager
    Support a discipline and or provide a service individually or within a team of associates. May provide functional expertise to Line Unit and other QA Units in area of responsibility
  • Novartis Hiring Quality Control Specialist
    Responsible for the quality of the multichannel digital content delivered to customers. Partner with all teams to understand and implement systemic controls wherever possible, across the software supply chain, from design till release. Explore and adopt quality improvement tools or methodologies.
  • Work as Expert Scientific Writer at Novartis
    MSc, PhD, PharmD, or MD. experience in medical communications. Medical writing experience. Demonstrate a command of assigned therapeutic areas and expertise with assigned products.
  • Work as Global Clinical Publishing Associate at Novartis
    Ensures a controlled documentation system, record retention, and information services including electronic records retention processes in accordance with regulatory requirements. Ensures compliance to the requirements from regulatory agencies. Maintains the technical and non-technical documentation change system.
  • Novartis looking for Analytical R&D Scientist - M.Pharm, MSc Apply
    Support Analytical project leader for setting analytical development strategy. Support in data interpretation, results compilations and sharing the information with critical observations and proposals to project team.
  • Require Analytical R&D Associate Scientist at Novartis
    Design, plan and perform scientific experiments for projects at different clinical phases of drug substance and drug product with minimal guidance. Well versed with regulatory guidelines, scientific literature, technology transfer and interpretation of the results to draw conclusions in reports.
  • Require Regulatory Affairs Manager at Novartis
    Provides the labeling, artwork strategy, regulatory intelligence and knowledge which are required to develop, market, and maintain products. Provides strategic labeling input and support for global development projects and, or marketed products
  • Require Product Specialist at Novartis
    Drive Competitive Sales Growth -Personalize and orchestrate customer engagement journeys for target HCPs by reflecting customer preferences, leveraging available content and multiple engagement channels
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