Vice President, Biologics

Responsibilities

• Establish and grow Syner-G's presence in the West Coast biologics market, specifically in the Bay Area, San Diego, and Seattle
• Leverage existing networks of biologics sponsors and CRO relationships to build pipeline
• Lead and execute biologics CMC consulting engagements as the primary technical point of contact
• Provide expert guidance on upstream/downstream process development, analytical characterization, and CMC regulatory strategy
• Author and provide strategic input on CMC regulatory submissions including INDs and BLAs
• Collaborate with senior leadership on proposal development, pricing, and scope definition

Requirements

• Advanced degree (Ph.D., M.S., or equivalent) in biochemistry, chemical engineering, pharmaceutical sciences, or related field
• 20+ years of biologics CMC experience, including time at a major biologics sponsor
• Deep technical expertise in at least two areas: upstream process development, downstream purification, analytical development, drug product formulation, or CMC regulatory affairs
• Proven track record of technical ownership on IND-enabling through late-stage or commercial programs
• Experience in business development or client relationship management at a CRO, CDMO, or consulting firm
• Extensive travel capability (up to 75–100%)

Preferred Qualifications

• Prior consulting or advisory firm experience in a fee-for-service environment
• Experience managing or mentoring junior technical staff

About the Company

Syner-G BioPharma Group is a strategic biopharma product development and delivery partner. We support organizations through critical phases of drug discovery, approval, and commercialization, helping to accelerate breakthrough science and deliver life-enhancing therapies to patients.