BioMarin is seeking a QA Operations Specialist to support documentation control processes within Quality Assurance and Quality Control. This role involves maintaining GMP compliance, managing document lifecycle, and ensuring efficient document flow, utilizing a Veeva Quality Management System. The position requires collaboration with cross-functional teams and adherence to regulatory standards.
Requirements
- 3+ years of experience in biotechnology or pharmaceutical industry....
Requirements: 3+ years biotech/pharma exp. BA/BS degree in life sciences, advanced degree desirable. Proficiency in Veeva EDMS and GMP/FDA regulations