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Sr. Quality Control Analyst (La Jolla/UTC)
By | November 30, 2007
Ceregene, Inc. focuses on the development of neurotrophic factor therapies for neurodegenerative disorders such as Parkinsons and Alzheimers diseases using viral vector gene transfer technology. Ceregene offers a collegial, entrepreneurial environment with opportunities for professional growth in addition to a competitive compensation and benefits package. Please visit www.ceregene.com.
Description:
The Sr. Quality Control Analyst is responsible for release testing in support of non-clinical and clinical viral vector products in compliance with GXP requirements. Establishes, modifies, and follows standard operating procedures (SOPs); performs release, stability, and in-process testing of materials, samples, and final products; works with mammalian tissue samples and cultures. Performs analysis and interpretation of test results, identifies deviations, and makes appropriate recommendations. Provides guidance to junior staff and applies technical and regulatory compliance knowledge daily.
Requirements:
Relevant scientific degree with minimum 5 years related experience in bio-pharma analytical laboratory. Experience in quality control strongly desired. Experience with viral vector (adeno-associated virus) product is a plus. Knowledge of cGMPs and regulatory requirements pertaining to biotechnology and pharmaceutical industries is required. Must have laboratory experience with a variety of analytical techniques including, but not limited to, quantitative PCR, ELISA, and cell-based assays. Proficient in general and non-routine laboratory skills. Good oral and written communication skills. MS Office skills; equipment related software such as Soft Max Pro desired.
For consideration, please email your resume as a Word document with Sr. Quality Control Analyst Job #07-012CL in the subject line to hr@ceregene.com. Your interest in Ceregene is sincerely appreciated.
EOE
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