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    Assistente de Assuntos Regulatórios - Sao Paulo, Brasil - MSD

    MSD
    MSD Sao Paulo, Brasil

    há 4 semanas

    Default job background
    Tempo integral
    Descrição

    Job Description

    Main Responsibilities:

    • Acknowledge the Health Agency's organizational structure and the main legislation in force.
    • Acknowledge of international documentations: CTD, cBPF, CPP, CCDS, sMA.
    • Health Authority legislation follow-up – updates and new legislation and impact evaluation.
    • Support in the evaluation and elaboration of dossiers for new marketing application (MA) and renewals of drug products and other products classification, if applicable (e.g., translation, elaboration and submission).
    • Support in the evaluation of technical documentation received from Global and / or partners in accordance with current sanitary legislation.
    • Support in activities related to artwork development (requirements, procedures, traceability of developed artworks, legislation, update systems and metrics).
    • Support in the evaluation of the impact of the labeling update received from headquarter.
    • Elaboration, adequation and update of leaflet text and minibula.
    • Artwork and leaflet development (QRD elaboration and revision; artwork revision and approval)
    • Support in the elaboration of Response to Question (RTQ) for Health Authority.
    • Participation in Pharma Trade Association meetings and in departmental meeting.
    • Support in regulatory intelligence, if necessary.
    • Request for GMP certificate for Anvisa.
    • Elaboration and implementation of Standards Operational Procedures (SOP), when necessary.
    • Archive skills (organization and maintenance)
    • Keep the company's local and global regulatory systems up to date.
    • Support to the department's intern in monitoring official publications (e.g. Official Gazette, ANVISA webpage, etc).
    • General support for Exportation certification requisitions (CPP), when necessary.

    Requirements:

    • Education: Student of the health sciences, such as Pharmacy or Biomedicine.
    • Languages: desirable English Business.
    • Technological skills: MS Office (Word, Excel, Power Point)

    #LI-DNI

    Current Employees apply HERE

    Current Contingent Workers apply HERE

    Search Firm Representatives Please Read Carefully
    Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

    Employee Status:

    Regular

    Relocation:

    No relocation

    VISA Sponsorship:

    No

    Travel Requirements:

    No Travel Required

    Flexible Work Arrangements:

    Hybrid

    Shift:

    1st - Day

    Valid Driving License:

    No

    Hazardous Material(s):

    No

    Job Posting End Date:

    05/26/2024

    *A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

    Job Posting End Date:05/26/2024

    A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

    Requisition ID:R296309



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