Regulatory Affairs Manager - Oslo - Merck Gruppe

    Merck Gruppe
    Merck Gruppe Oslo

    1 uke siden

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    Øvre Ledelse/Rådgivning
    Beskrivelse

    Imagining the Unimaginable with Science and Technology

    We are a global community of innovators, passionate about enriching people's lives through our solutions in Healthcare, Life Science, and Electronics. Our diverse team thrives on curiosity and collaboration, shaping the future with science and technology.

    Your Role:

    As a Regulatory Affairs Manager in Norway, you will be the key partner for our stakeholders, overseeing the regulatory life cycle of our marketed products and leading the registration of new compounds, including Early Access Programs for innovative assets.

    Key Responsibilities:

    • Manage submission management from planning to approval, ensuring highest quality in regulatory applications.
    • Collaborate with cross-functional teams like quality assurance, medical affairs, and market access.
    • Build strong relationships with health authorities.

    Requirements:

    • Masters degree in pharmacy or related scientific field.
    • At least 4 years experience in pharmaceutical industry, showcasing solid grasp of local regulatory requirements.
    • Experience in reviewing promotional materials is a plus.
    • Strategic thinking skills to develop effective risk mitigation strategies.
    • Proficiency in English and Norwegian is a must.
    • Proactive team player with strong drive to excel and contribute.

    What We Offer:

    We celebrate diversity and believe it drives excellence and innovation, strengthening our ability to lead in science and technology. We create opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress.



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