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.
The topics must include:
IT/Virtualization
Enterprise Content Management
Laboratory Systems
Manufacturing Systems
Project Management
Quality Assurance & Auditing
Business Intelligence
Governance, Risk and Compliance
Enterprise Resource Planning
Product Lifecycle Management
Clinical Automation
Enterprise Quality Management
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.
Oracle and SAP preferred.
