Document Production Specialist at Pillsbury Winthrop Shaw Pittman

Nashville TennesseeJob DescriptionThe Document Production Specialist provides document processing services creating a variety of documents and materials using Microsoft Office Suite products and other firm supported software. KEY RESPONSIBILITIESUse word processing software and other technical applications to input edit format and spell-check documents as well as perform scanning clean-up and formatting of images and proofreading.Respond to inquiries regarding status of projects.Answer routine questions regarding basic applications and department procedures.Continually develop proficiency with document production software and technical applications. Other administrative duties may include answering calls creating file labels and name badges setting up electronic binders and assisting with other clerical tasks as needed.REQUIRED EDUCATION KNOWLEDGE & EXPERIENCECertification as a Microsoft Certified Application Specialist (MCAS) or be willing to obtain such certification.Accurate and proficient typing skills (minimum of 75 words per minute preferred).REQUIRED SKILLS AND ABILITIESStrong computer skills including proficiency with Microsoft Office software (Word Excel PowerPoint).Strong customer service and communication skills and the flexibility to handle any tasks that are needed.Excellent proofreading skills.Technical aptitude and willingness to learn new applications. Ability to follow directions and use good judgment to perform tasks under limited supervision.Ability to analyze tasks to organize prioritize and handle multiple projects and be able to function in a high production environment.PHYSICAL REQUIREMENTS Ability to sit and stand for extended periods.Ability to lift up to 25 pounds.Pillsbury Winthrop Shaw Pittman LLP is an Equal Opportunity Employer.If you require an accommodation in order to apply for a position please contact us at .Required Experience:IC Key Skills DRG,Acute Care,Adobe Acrobat,ICD-10,Records Management,Technical Writing,Clinical Documentation Improvement,Documentation Review,Sharepoint,cGMP,Document Management Systems,Document Management Employment Type : Full-Time Experience: years Vacancy: 1