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    Pharma Regulatory Affairs Job Opportunity | Teva Pharmaceuticals is hiring | B Pharm &M Pharm Graduates | Apply Now

    Pharma Job at Teva Pharmaceuticals | Regulatory Affairs Job Opportunity

    Looking for a Pharma Job in the regulatory domain? Teva Pharmaceuticals is hiring for a Regulatory Affairs Job role – Regulatory Affairs Associate I in Navi Mumbai. This opportunity is ideal for B.Pharm and M.Pharm candidates with 1–3 years of experience who want to grow in regulatory publishing and global submissions.

    • Position: Regulatory Affairs Associate I
    • Location: Navi Mumbai, India, 400706
    • Job ID: 64525

    About the Company

    Teva Pharmaceuticals is a leading innovative biopharmaceutical company, enabled by a world-class generics business. Whether it’s innovating in the fields of neuroscience and immunology or delivering high-quality medicine worldwide, Teva is dedicated to addressing patients’ needs now and in the future.

    Here, you will be part of a high-performing, inclusive culture that values fresh thinking and collaboration. You’ll have the room to grow, the flexibility to balance life with work, and the opportunity to improve health worldwide, together.

    Job Description

    Regulatory Affairs Associate I – RA publishing will participate in the publishing of different regulatory activities. The focus will be to ensure 100% quality and timeline of the submission. This role will be the primary interface with the Regulatory Affairs Associate.

    Key responsibility

    • Handle and submit eCTD regulatory documents for EU, US, and Canada
    • Work on post-approval submissions and ensure quality before sending to agencies
    • Prepare, review, and fix documents to meet regulatory guidelines
    • Coordinate with scientific teams for submission planning and publishing
    • Follow internal and global publishing standards
    • Have basic knowledge of ICH and eCTD guidelines
    • Use tools like Veeva Vault, Adobe Acrobat, and other publishing systems

    Qualifications

    • B. Pharm/M. Pharm/ Master of Life Sciences.
    • Total years of experience required for the role: 1-3 years (preferred Regulatory Publishing experience in the EU and US market).
    • Command over spoken and written English.
    • Sensitivity to the cultural diversity of a global organization.
    • Good understanding of regulatory IT systems.

    CLICK HERE TO APPLY ONLINE

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