Associate Vice President

Key Responsibilities

•Strategic Leadership:Define and execute biologics manufacturing strategy aligned with corporate and client goals

•Operational Oversight:Direct drug substance & drug product manufacturing across microbial and mammalian platforms

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

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

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

Industry Experience

•Strong experience working in biopharmaceutical manufacturing and CDMO operations, and global supply chain

•Expertise across drug substance & drug product manufacturing (small molecules, biologics, complex formulations)

•Proven track record in process development, scale up, technology transfer, and commercial manufacturing

•Experience leading multi site operations with successful global regulatory approvals (USFDA, EMA, MHRA, WHO)