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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.

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    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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