- Bend, Oregon, United States
- 3+ years
Support daily activities of Serán’s Quality Assurance department in GMP clinical manufacturing operations, including review and approval of records, investigations, CAPA, change control, and manufacturing floor support.
Responsibilities
- Implement and continuously improve the company’s quality systems
- Authorship, review, and approval of SOPs and associated documents
- Review and approve master batch records
- Review and release raw material and product records
- Oversee investigations, CAPA, and change controls
Requirements
- Bachelor’s degree in a scientific discipline