Sandoz Require Regulatory Affairs Specialist

Sandoz is a global leader in generic and biosimilar medicines, which are more affordable versions of brand-name drugs. The Swiss-based company was part of Novartis until October 2023 when it became an independent entity, and its products reach millions of patients worldwide. Sandoz also provides active pharmaceutical ingredients and has a portfolio of approximately 1,300 products, including over-the-counter medications and treatments for a wide range of conditions from cancer to the common cold.

Post : Regulatory Affairs Specialist

Job Description
• Manages medium to small level global regulatory submission projects.
• Provide submission and contribute to the technical related regulatory strategy, intelligence and knowledge required to develop, register, and maintain global products.
• Contribute to strategic and technical input /support to drive implementation of global systems, tools and processes to support global development projects and/or marketed products.
• Frequent internal company and external contacts.
• Represents organization on specific projects -Works on problems of moderate scope where analysis of situations or data requires a review of a variety of factors.
• Reporting of technical complaints / adverse events / special case scenarios related to Sandoz products within 24 hours of receipt -Distribution of marketing samples (where applicable)

Candidate Profile
• Cross Cultural Experience.
• 5+ years of relevant experience.
• Functional Breadth.
• Collaborating across boundaries.
• Operations Management and Execution.
• Project Management.
• Clinical Study Reports.
• Data Analysis.
• Documentation Management.
• Life sciences.
• Operational Excellence.
• Regulatory Compliance.

Additional Information
Experience : 5+ years
Job ID : REQ-10030798
Location : Mumbai (Office) (Sandoz)
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Research & Development
End Date : 15th September 2026