<br/>We are looking for a writer with extensive knowledge of the United States Life Sciences industry, with a focus on FDA regulated software validation to write a series of white papers for us.<br/><br/><br/><br/>The topics must include:<br/><br/><br/>IT/Virtualization<br/><br/>Enterprise Content Management<br/><br/>Laboratory Systems<br/><br/>Manufacturing Systems<br/><br/>Project Management<br/><br/>Quality Assurance & Auditing<br/><br/>Business Intelligence<br/><br/>Governance, Risk and Compliance<br/><br/>Enterprise Resource Planning<br/><br/>Product Lifecycle Management<br/><br/>Clinical Automation<br/><br/>Enterprise Quality Management<br/><br/><br/><br/>please bid if you have experience writing technical papers on these topics and we will pay you for any white papers or case studies already written.<br/><br/><br/>Oracle and SAP preferred.<br/><br/>