New job Looking for QA Supervisor – Operations in Morris Plains, NJ

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Group: JOBS 2.0: Job Search Career Networking Staffing. Post Resume -Get Paid by Employers at Resumark .com Subject: Looking for QA Supervisor – Operations in Morris Plains, NJ Landon Hamilton posted a job: Looking for QA Supervisor – Operations in Morris Plains, NJ "For more information please go to: http://www.dendreon.com/careers/ Search for: 735 – QA – Supervisor Operations To apply online, click on the job description and start the application process. If you have any questions, please contact us at Dendreon@rightthinginc.com. Dendreon Corporation is a biotechnology company focused on targeting and transforming lives through the discovery, development, and commercialization of novel therapeutics that may significantly improve cancer treatment options for patients. The company applies its expertise in antigen identification, engineering and cell processing to produce active cellular immunotherapy (ACI) product candidates designed to stimulate an immune response. Dendreon is headquartered in Seattle and has a manufacturing facility in New Jersey and is in the process of constructing facilities in Georgia and California. Dendreon is seeking a highly motivated individual as a QA Supervisor – Operations in our Quality Assurance department. This is an excellent opportunity for someone to participate in a fast-paced high volume production environment with high quality and regulatory standards. Efficiency, accuracy and excellent communication skills are essential to success in this position. General Summary: The QA Supervisor will provide leadership and support for the development and implementation of Quality Assurance Policies and Procedures. In addition, the Quality Assurance Supervisor will provide direct support to the Immunotherapy Manufacturing Facility as described below. -Reviews and approves GMP controlled documents including standard operating procedures. -Leads the site Material Review Board. -Issues batch records and labeling in support of immunotherapy manufacturing. -Provides for batch record review and disposition of immunotherapy products. -Performs lot packet review and disposition of raw materials. -Ensures initiation, investigation, and closure of lot related deviations, non-conformances, and CAPAs."

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