This senior leadership role is responsible for leading and expanding strategic regulatory partnerships with a strong emphasis on post-approval lifecycle management
Job Summary
This senior leadership role is responsible for leading and expanding strategic regulatory partnerships with a strong emphasis on post-approval lifecycle management.
The position requires building and developing a high-performing global team across the United States, India, and potentially Europe while driving operational efficiencies.
Syner-G BioPharma Group offers a culture that aligns with career growth, learning support, and significant real-world outcomes from science to delivery.
Matching Summary
This senior leadership role is responsible for leading and expanding strategic regulatory partnerships with a strong emphasis on post-approval lifecycle management.
Skills & Requirements
Must-have
15+ years Regulatory Affairs experience
Post-approval lifecycle management expertise
FDA and EMA regulatory framework knowledge
Global team leadership across US India Europe
Strategic business development and revenue growth
Nice-to-have
Experience evaluating European market entry
Strong cultural agility in diverse environments
Continuous improvement and innovation mindset
Thought leadership in regulatory strategy
Data-driven decision-making capabilities
Key Requirements
Bachelor's or Master's degree in Biology Chemistry or related field
15+ years progressive experience in Regulatory Affairs
Significant experience in post-approval and lifecycle management
Demonstrated experience working with FDA and international authorities