Job Description
📋 Description Lead cross-functional product quality activities across lifecycle. Act as main quality contact for development strategy and global supply. Ensure end-to-end compliance from clinical to commercialization. Support product transitions, tech transfers, and lifecycle management. Coordinate QA activities across markets (e.g., launches) and audits. Hybrid role requiring on-site presence in Morrisville, NC or San Diego, CA. 🎯 Requirements High-level education in pharmaceutical, biotech, or life sciences 10+ years in pharmaceutical and biotech products under GMP Proven experience transitioning development projects to future commercial setup Strong leadership with a proven track record with Health Authorities Deep understanding of GMP & GDP requirements and strategic planning Fluent in English with excellent communication and interpersonal skills 🎁 Benefits Generous time off policy Opportunity to attend popular conferences Emphasis on work/life balance Collaborative and team-oriented environment Making a positive impact to help ultra-rare disease patients
