Hi, Please reply me at [email protected]
Position : Sr. Validation Analyst Location : St. Louis, MO Duration :6+Months Contract Start :ASAP Skills : Required Skills: 1) Must have experience with writing, analyzing, executing, and approving FDA Validation documents. 2) Experience writing and reviewing executed detailed software testing plans needed. 3) Previous experience leading software implementation team on validation activities required. 4) Knowledge of pharmaceutical laboratory testing preferred. 5) 10 + years' experience in quality role for software implementation projects needed. Essential Functions of the Position: . Analyze Laboratory Information Systems(LIMS) Business/User Requirement Specifications . Analyze, Develop, and execute OQ/MQ and, if necessary, PQ plans and test cases . Execute OQ/MQ/PQ plans and test cases . Track validation activities and test results . Prepare detailed reports and design documents based on results . Resolve minor testing problems . Identify deviations and provide recommendations for resolution . Confer with management to determine LIMS system validation limits and objectives . Create, populate, and maintain database for tracking validation activities and test results . Assist with MQ design and testing methodology such as AQC sampling or other analytical methodologies . Resolve more complex testing problems THANK YOU, Anil kumar Technical Recruiter Technology Resource Group Inc. 3736 Hills-dale Court Santa Clara, CA 95051 Office: 408-709-1760 , Ext: 960 | Fax: 408-884-2409 Email: [email protected] | Web: www.tech-resource.com Gtalk: trg.anil | YIM : trganil -- You received this message because you are subscribed to the Google Groups "Oracle Users" 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/oracle-users. For more options, visit https://groups.google.com/d/optout.
