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Quality Engineers # 949
By | November 25, 2009
The Company is an early-stage privately-held biotechnology company, focused on developing and commercializing a point-of-care molecular diagnostic assay platform, employing real-time PCR and automated sample processing methods
Senior Level and Entry Level
Responsibilities
o Implementation of cGMP quality system for Medical Device developer and manufacturer
o Ensure development activities are follow design controls
o Coordinate product submissions to various regulatory agencies
Requirements
o 4 year degree
o 1-3 / 5-8 years experience in Medical Device, BioTech, or Pharma
If interested please send resume to recruit@alcockmcfadden.com
Topics: San Diego Biotech jobs | No Comments »
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