Job Description
- 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
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