*Mail me your updated resume on [email protected] <[email protected]>*
Hello, We are currently looking for “*Validation Engineer”*. Please find the Job description below and contact me at your earliest possible convenience. *Role: Validation Engineer* *Duration: **6+ Months* *Location: Irvine, CA* *Required:* *Technical Skills* · Working knowledge of cGMP guidelines, FDA 21 CFR Part 820/210/211, ICH guidelines · Writing IQ, OQ and PQ protocol and report and execution for Chamber validation using Honeywell EMS. · Engineering change order · Development of a Standard Procedure (SP), related Work Instructions (WI), Forms, Checklists, Protocols, Reports & Templates for facilities/utilities, warehouse commissioning and qualification activity · Writing IQ, OQ and PQ protocol and report of computer system validation. *Experience Required * • Medical devices and process validation experience Thanks and Regards, Chandrashekhar Kumar Technical Recruiter Diverse Lynx, LLC Phone: 732-452-1006 Extn 265 Fax: 732-452-0684 Email – [email protected] -- You received this message because you are subscribed to the Google Groups "SAP Resource Center" group. To unsubscribe from this group and stop receiving emails from it, send an email to [email protected]. To post to this group, send email to [email protected]. Visit this group at https://groups.google.com/group/sap-resource-center. For more options, visit https://groups.google.com/d/optout.
