Hi We have the below contract job opportunity with one of our direct clients. Please send across the resume along with the contact information at the earliest to kanhaiya.pan...@acsicorp.com or call me at 678-207-5255
Location - Minneapolis, MN Role: Validation Engineers with IQ/OQ/PQ Job Description: Medical Device mechanical component test method verification and validation. Key Skills: Experience in IQ/OQ/PQ, TMV. Experience in Validation, CAPA, FMEA Additional Skills: · Creating and updating design documentation for medical devices (DHF/ DMR), ECR/ ECN creation, review · Creating, updating controlled drawings and BoM? PDM/ PLM tools - Windchill, Enovia, Factory works, Agile etc · ISO 13485, design control processes Experience/ Requirements · B.S. in Mechanical Engineering or Technology · Experience in medical device product development experience · Experience in any PLM/ PDM tool - Enovia preferred · Knowledge of FDA 21 CFR Part 820 compliance & ISO 13485 Standards *Please send your word format Resume along with below detail:-- * Full legal Name : Best Contact Number and Time to reach you: Email Id : Current Location: Open to Relocation : Visa Status (visa expiration date): Availability to start (End date of project): Available for interview (timing) : Highest Qualification with Year : Skype Id: Thanks and Regards, Kanhaiya Pandey *ACS Global Services* | 2400 Meadowbrook Parkway; Duluth, GA 30096 Phone 678-207-5255 kanhaiya.pan...@acsicorp.com *|| *www.acsicorp.com Gtalk: adamseansm...@gmail.com [image: Description: Description: Description: http://www.acsicorp.com/images/acsggslogo.png] -- You received this message because you are subscribed to the Google Groups "oraapps" group. To unsubscribe from this group and stop receiving emails from it, send an email to oraapps+unsubscr...@googlegroups.com. To post to this group, send email to oraapps@googlegroups.com. Visit this group at http://groups.google.com/group/oraapps. For more options, visit https://groups.google.com/groups/opt_out.
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