Vice President

Key Responsibilities
•Strategic Leadership: Define and execute CMC vision aligned with corporate growth and client needs
•Operational Excellence: Oversee drug substance & drug product development, scale‑up, validation, and lifecycle management
•Regulatory Stewardship: Ensure GMP compliance and lead CMC documentation for USFDA, EMA, MHRA, WHO submissions
•Client Engagement: Act as senior interface with global pharma/biotech partners, driving delivery on time, cost & quality
•Talent Development: Build and mentor high‑performing scientific and operational teams, fostering innovation and compliance culture
 
Industry Experience
•Strong experience working years in pharmaceutical R&D, manufacturing, and CMC leadership
•Deep expertise in route design, optimization, scale-up.
•Strong track record in client-facing program execution (FTE/FFS).
•Experience with regulatory-driven drug substance development (IND/NDA/DMF).
•Leadership of large technical teams
•Proven track record in leadership, global regulatory approvals, and strategic partnerships