Hi Partner, Please share suitable resumes ASAP on [email protected]
*Validation Engineer* *Duration: 6 months+* *Location: Foster City, CA* Experience in Software Development Lifecycle (SDLC). Experience in QA Methodologies, designing, reviewing and approving Test Plans, systems and UAT test scripts and Test procedures. Experience with in Change Control processes. Experience with various FDA regulations (e.g. 21 CFR Part 11, 210, 211, 820) Experience is creation of SOPs. Knowledge of FDA guidance’s and industry standards (i.e., GAMP) Hands on experience in HP Quality Center and QTP. Strong verbal and written communication skills. Perform assessments of computer systems and processes at client sites (compliance with internal procedures, industry best practices, and regulatory requirements) Develop validation strategy documents, write user requirements, SOPs, IQ/OQ/PQ, and create validation summary reports Thanks and Regards, Nishant Bhardwaj e-Solutions Inc Email: [email protected] Phone: 408-618-5052 Gtalk ID:nishant.recruiter111 Yahoo ID:recruiter.nishant111 -- You received this message because you are subscribed to the Google Groups "only.SAP" 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 http://groups.google.com/group/onlysap. For more options, visit https://groups.google.com/groups/opt_out.
