Experience working in FDA regulated environment is preferred. 
Past experience writing, reviewing and executing computer validation documentation (Validation
Plan, IQ, OQ, PQ, RTM, summary report). 
Excellent communication skills. 
Ability to work as a team player in a consulting environment. 
With a willingness to travel, relocation is not necessary. 
For direct and contract positions. 
Must be willing to work extended hours (overtime is paid for). 
Proficiency with MS Office tools 
Documentation management