Job Description:
• Provides technical and analytical expertise for late phase biologics process development and commercial manufacturing activities for multiple technology areas (e.g. cell banking, cell culture, purification, formulation, or bioconjugation)
• Responsible for managing projects in multiple technological areas at external CDMO partners
• Acts as the Biologics lead for a specific therapeutic program
• Communicates with cross-functional teams in formal settings and third-party meetings
• Supports the international roll-out of approved prostate cancer imaging agent and helps advance portfolio of late clinical-stage products
Requirements:
• Science or engineering degree with minimum relevant experience as applicable: BS with 11+ years of experience, MS with 9+ years of experience, PhD with 8+ years of experience.
• 6+ years of experience in GMP, quality management system, and CMC compliance and regulation.
• Demonstrated understanding and application of project management principles and tools.
• Ability to work in cross-functional, virtual teams.
• Travel expectation: 10 – 25% for key in-person meetings, partner site visits, and SME/technical person-in-plant assignments.
Benefits:
• Competitive salaries
• Annual performance-based bonuses
• Equity-based incentive program
• Generous vacation
• Paid wellness days
• Support for learning and development