About this role
Senior Director, Corporate Quality – PV at Sarepta. Location: Bedford, Massachusetts, United States. Role: designing audits, overseeing audits, performing investigations Requirements: Bachelor's in life sciences with ~15 years in pharma/biotech drug development; minimum 10 years GCP/GVP QA (≥5 years focused GVP QA); clinical trial and inspection experience; QMS, SOPs, audit design, root-cause investigations, and strong technical writing skills. Category: Quality Assurance Seniority: Senior Level Commitment: Full Time Workplace: Hybrid Languages: English