*Validation Specialist *Location : Foster City, CA Duration : 6 + months ******For Immediate feedback please forward your resume to [email protected] <mhtml:mid://00000252/> ******** *
*MUST HAVE Bio-pharma experience* REQUIREMENTS: Validation Specialist: Must be able to lead projects and work independently, as well as be very hands on writing scripts, manage testing activities, configuration, etc. Candidate has to be strong in Validation Test execution Create and execute validation test scripts and document test results in accordance with standards (Functional Testing, formulate tests and document and run tests) Experience in writing and executing software test strategies, protocols, and test cases within a formal Software Life Cycle (SLC) process Review/revise Validation documents as directed Solid knowledge of FDA regulatory requirements, including 21 CFR Part 11 Outstanding communication skills Thanks and Regards*. . .** *** *Neev Roy ,* Sr. Technical Recruiter, Office: (201) 257 5081Ext : 283 || Fax: (201) 727 9296 [email protected] <mhtml:mid://00000252/> || [email protected]<mhtml:mid://00000252/> www.catamerica.com <mhtml:mid://00000252/> || www.cattechnologies.com<mhtml:mid://00000252/> -- You received this message because you are subscribed to the Google Groups "CorptoCorp" 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/corptocorp?hl=en.
