*Dear Partner,*
*Please share suitable resumes ASAP on
*
*nishan...@e-solutionsinc.com <nishan...@e-solutionsinc.com>*
*Validation Analyst ( Laboratory system experience)*
*Memphis TN*
*Rate: 50-55/hr*
*Note : NO EAD OPT CONSULTANTS PLEASE*
• Significant experience in Quality and Compliance with substantial
hands-on computer system validation experience
• Experience in *FDA* regulated environment with good understanding of GxP
related processes including Risk Based validation
• Experience with Change Control processes
•
• Knowledge of FDA guidance’s and industry standards *(e.g. GAMP, Quality &
Compliance, FDA regulations & international regulations* *(e.g. 21 CFR Part
11, Part 820, Annex 11), LIMS*
• Experience with Change Control processes
• Hands on experience in *HP Quality Center and QTP*
• Strong verbal and written communication skills
• Able to work as a team player, lead a team or accomplish tasks without
supervision.
• Ability to work with remote teams and support several changes/projects
simultaneously.
Thanks and Regards,
Nishant Bhardwaj
e-Solutions Inc
Email: nishan...@e-solutionsinc.com
Phone: 408-618-5052
Gtalk ID:nishant.recruiter111
Yahoo ID:recruiter.nishant111
--
You received this message because you are subscribed to the Google Groups
"only.SAP" group.
To unsubscribe from this group and stop receiving emails from it, send an email
to onlysap+unsubscr...@googlegroups.com.
To post to this group, send email to onlysap@googlegroups.com.
Visit this group at http://groups.google.com/group/onlysap.
For more options, visit https://groups.google.com/d/optout.
