About this role
Senior Quality Specialist at Element. Location: Concord, California, United States. Role: ensuring compliance, reviewing documentation, conducting audits Requirements: 6+ years pharmaceutical/biotech/GMP quality experience preferred; knowledge of ISO 17025:2017, USP, CGMP, FDA and ICH; perform audits, investigations, CAPA, deviations, and data review. Category: Research and Development (R&D) Seniority: Senior Level Certifications: iso 17025:2017 Commitment: Full Time Workplace: Onsite Languages: English