Company DescriptioneTeam was formed in 1999 with the goal of becoming the supplier of choice for clients, employees and contingent workers. Today, we’re one of the fastest-growing companies in New Jersey and ranked as one of the best companies to work for by Staffing Industry Analysts and New Jersey Business. We’re also an honored member of Deloitte’s Technology Fast 50Job DescriptionAccountable for administration of the Change Order (CO) process.Accountable for compliance with the Food and Drug Administration's (FDA) Quality System Regulation (QSR) as it pertains to Documentation and Documentation Control.Accountable for the timely processing and release of new and changed controlled documents.POSITION DUTIES & RESPONSIBILITIES:Accountable that all Change Order s (CO) are reviewed for completeness, accuracy and compliance with applicable policies and procedures.Coordinate workflow and Client Synthes priorities of Document Control West Chester with management and Change Owners on an as needed basis.Communicate CO status information as requested.Administer the Periodic Review process for controlled Quality documentsManage Designated Alternate Signature formsProactively seek methods of increasing efficiency while maintaining compliance in all areas of responsibility on a continuing basis.Provide historical and current documentation in response to queries from management and other departments as needed.Exhibit excellent organizational and communication skills.Properly employ all Synthes SOPs, Work Instructions, Training Guides, and Forms in the performance of tasks.Maintain a work environment that provides open communication and personnel growth.Be an extremely flexible team player, adaptable to change.Be customer service oriented and experienced at interacting with individuals at all levels, including upper management.Perform other special projects and support functions as assigned by the Manager of Document Management.Required to know and follow all laws and policies that apply to one's job, and maintain the highest levels of professionalism, ethics and compliance at all times.Diligently participate in our compliance program-related activities as denoted by supervisor or our Chief Compliance Officer.QualificationsA minimum of a Bachelor Degree is required.A minimum one year (professional, intern or co-op) in a GMP and/or ISO regulated environment is required.Familiarity with various PC-Based viewing systems (WebView, Product View, Agile etc.) is required.Proficient with Microsoft Office products (Word, Excel, Power Point, etc.) is required.Previous document control experience is preferred.Medical device, Pharmaceutical and/or Biotech experience is preferred.Proficient with various PC-Based CAD systems (Pro/Engineer, Windchill, Medusa, AutoCAD, etc.) is preferred.Additional InformationThanks & RegardsNeha SharmaLead RecruitereTeam Inc – “ACCELERATED HIRES”Efficiency, Synergy, ExpertiseT-732-248-1900 .Ext 120Awards#1 Best Places to work in New Jersey-2009,2008,2007,2006 Top Small Diversity Business, 2006 by DiversityBusiness.comDeloitte Technology Fast 500-2007,2006IMPORTANT NOTE: Under Bills.1618 Title III passed by the 105th U.S. Congress, this email cannot be considered spam as long as it contains our contact information and a link for the removal requests. If you have received this mail in error or prefer not to receive such emails in the future, please reply with "REMOVE" in the subject line and the email id(s) to be removed. All removal requests will be honored ASAP. We sincerely apologize for any inconvenience caused.