Document Control Administrator West Point, PA Consulting Interested candidates should send a Word copy of their resume with geographic preferences and availability to sabithash@kleinmgmt.com * Applications are sought for a scientist position in the Research Laboratories - Bioprocess Clinical Manufacturing and Technology. * Candidate must have strong organizational, multi-tasking, attention to detail, and communication skills. * Experience working with regulated documents is desired. * At least 2 years of relevant experience with document management and/or training management systems is desired. * Candidate must successfully complete job position assessment. Responsibilities: * Individual will support document management and training management systems for bulk biologic clinical supply process and analytical activities in the Bioprocess Research & Development area. * As necessary, candidate will participate in a range of activities including, but are not limited to; coordination of official document systems (i.e., Standard Operating Procedures, Assay Procedures, Guidelines, Position Papers, Batch Records), and coordination of area's training activities with Company's global training system as well as internal electronic tracking system (e.g. SOP Training, Restricted Access Training, New Employee Training, and GMP Training). * Candidate is expected to work in a team atmosphere in close collaboration with analytical and process development staff; pilot plant staff and support groups; Safety and Environmental, and GMP Quality.