About this role
In Process QA Associate at Nivagen Pharmaceuticals. Location: Sacramento, California, United States. Role: monitoring processes, line clearances, documentation review Requirements: Bachelor’s in Life Sciences or related field OR equivalent GMP manufacturing experience; 0–3 years in sterile pharma; knowledge of cGMP/FDA 21 CFR; strong organization and communication; familiarity with deviation, CAPA, change control; experienced with eQMS; MS Office proficiency. Category: Quality Assurance Seniority: Entry Level Tools: ComplianceWire, TrackWise, SAP, LIMS, eQMS, Microsoft Office Commitment: Full Time Workplace: Onsite Languages: English