Pharmaceutical manufacturing and research co. (Sacramento, CA) seeks qualified professional to prepare protocols of analytical method validation / verification and plan the analysis and prepare reports after completion of activities. Handle and track OOS (out of specification) and OOT (out of trend) investigations and prepare investigation reports. Participate in USFDA, EU, TGA, ISO13485 and WHO audits. Adhere to SOPs and review audit trail of QC instruments. Send resumes to: HRD, Nivagen Pharmaceuticals Inc., 3050 Fite Circle, Suite 100, Sacramento, CA 95827
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