Solvita seeks a seasoned BLA Quality Assurance Director to lead Pre-License Inspection readiness for biologics manufacturing sites. You will drive cGMP enhancements, coordinate with client teams, and oversee QA activities across multi-client programs to ensure inspection readiness and compliant submissions.
The role requires 12+ years in biologics QA, leadership in BLA filings, and strong experience with regulatory interactions and data integrity.
#J-18808-LjbffrBLA Quality & Regulatory Lead — PLI Readiness in kettering at Unknown Company
This position is listed as full time and onsite.