Sandoz Healthcare/BioTech

Regulatory Affairs Specialist – GMP

India In person Full-time

Location: Telangana (Sandoz)

Job Description Summary

Sandoz continues to go through an exciting and transformative period as a global leader and pioneering provider of sustainable Biosimilar and Generic medicines. As we continue down this new and ambitious path, unique opportunities will present themselves, both professionally and personally. Join us, the future is ours to shape!

Provide effective operational and regulatory support to evaluate, submit and maintain GMP clearanc-es for existing and new manufacturing sites in the best possible time frame and to ensure compliance with all corporate and local requirements.

Partner with relevant stakeholders to assist in achieving optimal company outcomes.

Regulatory Information Management (RIM) on relevant systems, trackers and databases for regula-tory submissions and commitments.

  • Stakeholder Relationships

Job description provided by Sandoz.
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