Vice President

Key Responsibilities

•Strategic Leadership:Define and execute formulation development roadmap aligned with client and corporate goals

•Operational Oversight:Direct formulation R&D, scale up, and clinical trial material production

•Regulatory Stewardship:Ensure CMC compliance, GMP standards, and regulatory submissions

•Client Engagement:Senior interface with global pharma/biotech clients, ensuring delivery on time, cost & quality

•Talent Development:Build and mentor scientific teams, fostering innovation and compliance culture

Industry Experience

•Strong experience working in pharmaceutical R&D, formulation science, and CDMO operations

•Expertise across oral solids, injectables, and specialty dosage forms

•Proven track record in clinical manufacturing, technology transfer, and lifecycle management

Experience leading multi site formulation teams with global regulatory approvals (USFDA, EMA, MHRA, WHO)