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Sant Joan Despí

    Quality Admin. Support - Sant Joan Despí, España - Neuraxpharm

    Neuraxpharm
    Neuraxpharm Sant Joan Despí, España

    Encontrado en: Buscojobs ES C2 - hace 5 días

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    Descripción

    Neuraxpharm is a leading European specialty pharmaceutical company focused on the treatment of central nervous system disorders (CNS) with a direct presence in 20 countries. Backed by funds advised by Permira, Neuraxpharm has a unique understanding of the CNS market built over 35 years.

    With its focus on CNS, Neuraxpharm develops and commercializes established brands, value added medicines, generics, Consumer Healthcare products, medical cannabis, beyond-the-pill solutions (digital health and medical devices) and orphan drugs and is continuously striving to offer a wide range of effective, high quality and affordable CNS treatment options in Europe.

    Present with its products in more than 60 countries, Neuraxpharm also manufactures pharmaceutical products and active pharmaceutical ingredients in its own manufacturing sites, Lesvi and Inke, in Spain. For more information, please visit

    Neuraxpharm is searching a vacancy based in Sant Joan Despí:

    QUALITY ASSURANCE SUPPORT

    Participate in a project to update the documents of the company due to a change , modify documents, monitor status of advancement of the changes of all documents and record according to the internal procedures of the area and the requirements of the pharmaceutical industry (GMPs) His/her main responsibilities will be:


    • Modification of all GMP documents to load in the QMS ShareMe due to a change in the company GMP related documentation of the quality department:

    o key user of the GMP document management system ShareMe for all GMP related documents o distribution of GMP related documentation to all GMP related departments.


    • Reporting indicators of the evolution of changes.


    • Report the completed activities in the Change Control request.

    SPECIFIC ACCOUNTABILITIES


    • Expert in word management to modify lay out documents and all word functionalities to complete a fast process and with tapping errors.


    • Key user of the GMP document management system ShareMe.

    WE REQUIRE:


    • Minimum demonstrable experience of more than 4 years of experience in assistant work


    • Experience in the pharmaceutical sector will be an asset.

    WE OFFER:


    • Individual Professional development in a leading European pharmaceutical company with an ambitious international growth strategy.


    • Economic conditions will be according to the experience and skills provided.


    • A motivated and committed environment based on a diverse and inclusive culture.

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