Write detailed test plans and reports for QA testing of raw materials and IVD products under development
Summarize product specifications, QC results, and other technical data for DNA Typing and Antibody Detection assays
Verify accuracy of information by referring to master documents, raw data, or software output
Track PD requirements against experimental data and create, organize, and file reports
Review product performance or stability test results for conformity and established specifications
Track projects to completion. Work with laboratory technicians to keep detailed log of on-going studies
Assist in process improvements for document and data management in the PD Division
Assist with FDA filings PDV/V Test plans reports, tabular graphic format
Responsible for assisting ONLY with graphs, tables, templates, charts, suggested document layout, etc.
Contact:Wanda J. Reese
Jade Medical Communications Group, LLC
Medical Writer Consultant12021 Wilshire Blvd., #296Los Angeles, CA 90025-1206
The jobs listed in the Biotech Ink Insider weekly newsletter come to Susan Caldwell mostly by word-of-mouth and contact with hiring managers and recruiters. 
