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Implementation, monitoring and evaluation of GLP-compliant preclinical biocompatibility studies. Job specific tasks include protocol preparation, data evaluation, interpretation, reporting, and the generation of final reports.
Qualified individuals must be highly motivated with three to five years previous industry experience. They must be able to manage multiple projects and correspondence with clients in an efficient and timely manner. A bachelor's degree in a biological science or related field is required.
Preferred candidates will have a strong working knowledge of GLP regulations and preclinical testing facility operations and procedures, as well as an understanding of ISO 17025 and ISO 10993 guidelines.