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    Regulatory Affairs Specialist

    REQ-10058966
    7月 30, 2025
    Saudi Arabia

    摘要

    Be the bridge between innovation and patient safety—As a Regulatory Affairs Specialist in Saudi Arabia’s dynamic healthcare landscape, you’ll play a pivotal role in shaping the future of medicine. From ensuring compliance with SFDA regulations to accelerating access to life-saving therapies, your expertise drives both public health and industry growth. Join a mission where precision meets purpose, and every regulation you navigate brings better care to millions.

    About the Role

    Major Accountabilities 

    • New Product Registrations – With supervision, evaluate, and prepare drug registration applications in a timely manner and follow through the application during the evaluation phase to achieve a favorable outcome
    • Maintenance of registered products – With supervision, maintain registration of currently approved products (initiation and preparation of variation/ and renewal applications as per the plan communicated from the DRA manager/Head).
    • Coordinate with DRA manager/head to ensure correct and speedy implementation / consignments as per the approved applications (variation/ renewal/ site transfer/ site registration/leaflet update).
    • Maintain, with supervision, the internal DRA database accurate and updated: Dragon/DASA
    • Relationships within and outside the company - Develop and maintain good working relationships with other Novartis departments both locally and with Head Office and with third-party vendors.
    • With Supervision, Review PPMS and ensure AQWA Launch request are prepared and launched on time.
    • With Supervision, ensure full support to Global regulatory compliance initiatives in Saudi.

    Minimum Requirements

    • Pharmacy or related science degree.
    • Minimum 1 year of RA Experience in reputable pharmaceutical company.
    • Experience handling a portfolio/product and dealing with stakeholder such as SFDA and governmental agency.
    • Must be Saudi national.


    #LI-Onsite

    Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture

    Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network

    Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards

    Development
    Innovative Medicines
    Saudi Arabia
    Riyadh
    Research & Development
    Full time
    Regular
    No

    Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

    REQ-10058966

    Regulatory Affairs Specialist

    Apply to Job

    Source URL: https://www.wanpudi.com/careers/career-search/job/details/req-10058966-regulatory-affairs-specialist

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    1. https://www.novartis.com/about/strategy/people-and-culture
    2. https://talentnetwork.novartis.com/network
    3. https://www.novartis.com/careers/benefits-rewards
    4. https://novartis.wd3.myworkdayjobs.com/en-US/Novartis_Careers/job/Riyadh/Regulatory-Affairs-Specialist_REQ-10058966
    5. https://novartis.wd3.myworkdayjobs.com/en-US/Novartis_Careers/job/Riyadh/Regulatory-Affairs-Specialist_REQ-10058966