Hi Partners, Please find below urgent requirement and kindly send me suitable profiles ASAP
*Location – Stamford CT* *Duration 6- 12 months* **** * * *SW Validation Specialist* Our client is looking for SW Validation specialist. They are on the verge of implementing SAP and a Service Management tool called Astea. Both of these systems will have to meet FDA regulations. *Position Requirements:* Strong knowledge of the computer validation aspects of current Good Manufacturing Practices cGMP). Knowledge of all regulations including (CFR 21 Part 11). Either pharmaceutical or medical device experience is a must. Must have ERP experience, preferable SAP. This experience should include the full lifecycle of a validation project from requirements through protocol summary report. Strong interpersonal and writing skills as well as have the ability to communicate effectively with both the business and information technology. Be able to provide leadership in the area of computer validation and direct the validation efforts of a project. At the same time as providing leadership, willing to complete deliverables. Thanks and Regards, Anil Kumar TRUSTEK INC | 6 Kilmer Road, Suite # Q, Edison, NJ | Work: (732) 393-1313/ (732)-377-8993 Ext: 106 | Fax: (866)-294-1314| [EMAIL PROTECTED] | www.trustek.com | ================================================================ If you don't want to receive emails any longer - just reply with "REMOVE" in subject line ================================================================ --~--~---------~--~----~------------~-------~--~----~ You received this message because you are subscribed to the Google Groups "Oracle-Distribution" group. To post to this group, send email to [email protected] To unsubscribe from this group, send email to [EMAIL PROTECTED] For more options, visit this group at http://groups.google.com/group/Oracle-Distribution -~----------~----~----~----~------~----~------~--~---
