We are driven by a relentless pursuit of bold science to translate genetic discoveries into new medicines. Our scientific expertise has led us to create transformative medicines using various treatment modalities.
The Technical Operations team builds and maintains cutting-edge manufacturing processes and sites, providing quality assurance and control. The team procures goods and services to support manufacturing and coordinates the worldwide movement of drugs to patients.
The QADC Associate is part of this team and is responsible for maintaining site quality systems, providing quality oversight of facilities with a focus on document management and quality systems.
Key responsibilities include process-controlled documents on Document Control Systems, approving document change controls, establishing effective dates, completing work according to priorities and policies, and supporting Inspection Readiness for sites.
The ideal candidate will possess strong communication and organizational skills, experience with Quality Management Systems and Electronic Document Management Systems, and ability to examine Quality Metrics related to Document Control Systems. They will also participate in Continuous Improvement for the Quality Team and perform other duties as requested.
We welcome applications from qualified candidates without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and disability. To be considered for this role, please complete the application process on our careers page.