Hello, Hope you are doing well, Please go through the following requirement and let me know on ke...@riderconsultinginc.com if you have any available resources
Role:IT Quality Validation Opportunity *Experience with Argus or Aris G REQUIRED* Location:Woodcliff Lake, NJ (MUST BE ABLE TO INTERVIEW FACE TO FACE) GREEN CARD, OR US CITIZEN! I have a new need for a Safety Systems Validation Consultant for a yearlong contract opportunity in Northern NJ. Career Developers is searching for a 12 month + Contract IT Quality Validation Analyst/Tech Writer for a Pharma co in Northern NJ. Candidates will: Prepare computer validation documents such as Validation Plans, User Requirements, Configuration Specifications, Test Protocols, and Summary Reports. Prepare Change Control documentation. Execute test scripts. Perform risk assessments. Must be familiar with 21 CFR Part 11. Consult on Projects. Prepare Project Plans. Must have BS in a technical field and 5 years' experience in GxP environment. Pharmaceutical Experience. Experience in writing IT system documents such as IQ/OQ and PQ's. Understanding of SDLC and IT/system change management processes. Experienced in writing system implementation project test cases and other project related documents. Thanks. Kevin*Patel* Ph No:- 980-819-0687 E-mail:- ke...@riderconsultinginc.com G-Talk : kevinpatel.ri...@gmail.com Web Site :- www.riderconsultinginc.com -- You received this message because you are subscribed to the Google Groups "Citrix and Sap problems" group. To unsubscribe from this group and stop receiving emails from it, send an email to citrix-and-sap-problems+unsubscr...@googlegroups.com. To post to this group, send email to citrix-and-sap-problems@googlegroups.com. Visit this group at http://groups.google.com/group/citrix-and-sap-problems. For more options, visit https://groups.google.com/d/optout.