About Our Client

Our client is a leading pharma MNC.

Job Description
- Lead regulatory affairs and affiliate quality activities across India and neighboring countries, ensuring compliance with local regulations and company standards.
- Develop and execute regulatory strategies to support recent product registrations, lifecycle management, market expansions, and product imports.
- Manage interactions with regulatory authorities and industry bodies to facilitate approvals, influence policy discussions, and maintain compliance.
- Provide regulatory guidance to commercial, technical, clinical, and cross-functional teams on product development, claims, labeling, promotional materials, and business initiatives.

The Successful Applicant

We're looking for someone who has:
- 15+ years of Regulatory Affairs experience within pharmaceuticals, biologics, vaccines, or animal health.




- Proven track record of leading product registrations, regulatory compliance, and lifecycle management activities.
- Strong experience interacting with regulatory authorities, government bodies, and industry associations.
- Demonstrated people leadership experience, with the ability to build, mentor, and develop high-performing teams.
- Deep understanding of regulatory frameworks, quality systems, import/export regulations, and compliance requirements.

What's on Offer

This opportunity offers the chance to lead Regulatory Affairs, while playing a pivotal role in shaping regulatory strategy, enabling new product launches, supporting market expansion, and influencing business growth.

📌 Associate Director- Regulatory Affairs (Mumbai)
🏢 Michael Page
📍 Mumbai