Accuray to Cut 5 Pct.of Jobs to Reduce Cost - Nov. 16, 2011

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Wednesday, November 16, 2011  |   |   |   |  The Master of Science (MS) in Medical Product Development Management (MPDM) at San Jose State University is a comprehensive, master's degree program and can be completed in either 2 or 3 years. The emphasis of the program is on the management of products undergoing clinical research and clinical development, i.e. clinical trial stages I, II, III and IV or other testing as required by the Federal Food and Drug Administration (FDA) or international regulatory authorities. The curriculum includes customized courses from the Colleges of Science and Business, and was designed in consultation with biomedical industry employers in the greater San Francisco Bay area. The MPDM program continues to have interaction with the industry and provides expert industry speakers in the classroom, in order to present the latest advancements to students. Please click here for more information.   •  Accuray Inc. (ARAY) to Cut 5 Pct. of Jobs to Reduce Cost More... •  Tandem Diabetes Care Announces FDA Clearance of the t:slim™ Insulin Delivery System More... •  W. L. Gore & Associates, Inc. Receives FDA Approval for Conformable GORE® TAG® Thoracic Endoprosthesis More... •  FDA Clears PositiveID (PSID)'s iglucose System for Diabetes Management More... •  CooperVision Inc. Announces Expanded Recall of Avaira Line of Contact Lenses More... More Top News Marcus Evans: 2011 Navigating 510(k) and PMA Submissions and Approvals" November 17 - 18, 2011 Chicago, Illinois U.S.A. This premier Marcus Evans conference will address potential regulatory changes in the PMA and 510(k) submission and approval process and provide regulatory affairs executives knowledge on how to streamline their submission processes by anticipating FDA requirements. 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CLIA Lab Director Responsible for the overall operation and administration of the Veracyte CLIA laboratory, including employing/supervising personnel who are competent to perform test procedures; generating test results and patient reports promptly, accurately and proficiently; and assuring compliance with the applicable state and federal regulations. • BioForest (Bothell, Washington) Alder Biopharmaceuticals Fermentation Development Engineer This position reports to the Director of Fermentation and the individual will perform hands-on operations for the development of yeast based fermentation and harvest processes for the production of therapeutic monoclonal antibodies. • Genetown (Worcester, Massachusetts) Abbott Principal Engineer Will lead a technical support group of 6-8 engineers and associates engaged in process engineering, technical transfer, manufacturing support and exception report management. The technical support group works directly with a cell culture and purification production group within a business unit. • Biotech Beach (Irvine, California) TEVA Pharmaceuticals USA Quality Systems Engineer I/II/III Responsible for reviewing or approving the validation of product, equipment, process, and laboratory equipment and or QC methods. Provides Quality Assurance oversight to facilities, maintenance, engineering and/or QC laboratories. The QE II will have the ability to collect data, analyze, and identify the most important parameter affecting product quality and will implement preventive/corrective action plans (root cause analysis); as it relates to a variance, complaint, and OOS investigation. • Pharm Country (Tarrytown, New York) Regeneron Pharmaceuticals, Inc. Laboratory Systems Engineering Leader Responsible for the planning, design, implementation and maintenance of computer systems utilized in the laboratory areas of the company. 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