Sarepta Therapeutics is seeking a Director, Corporate Quality to lead GCP/GLP QA across Clinical Development and Real-World Evidence. You will ensure FDA/ICH compliance and partner with Clinical, Pharmacovigilance, and Research teams to uphold patient safety and scientific integrity. In this hybrid role, you will drive CAPA programs, audits, inspection readiness, and continuous QMS improvements while supporting external and internal audits and regulatory inspections.

Also on the board Same function, level within a rung

Level

Manager

Location

Somerville, MA

Occupation

Compliance Managers

Industry

Pharmaceutical Preparation Manufacturing

Posted

yesterday

Apply for this role →