Position Description:  

Sr. Quality Control Analyst #07-011ASGT
Responsible for release testing supporting non-clinical/clinical viral vector products in compliance with GXP. Establishes, modifies, follows SOPs; performs release, stability, and in-process testing of materials, samples, final products; works with mammalian tissue samples and cultures. Performs analysis, interprets test results, identifies deviations, makes appropriate recommendations.

Relevant scientific degree with 5 years experience in bio-pharma analytical laboratory. QC experience required, viral vector (adeno-associated virus) product a plus. Knowledge of cGMPs and regulatory requirements pertaining to biotechnology/pharmaceutical industries required. Experience with variety of analytical techniques - qPCR, ELISA, and cell-based assays required. Apply to hr@ceregene.com