*Hi...* I hope you are doing well. I am sending the new requirement, please go through it and let me know if you are comfortable and send me the *resumes to **[email protected]* <[email protected]>
*Position = VALIDATION TESTTER Location = Social Circle , GA ( Local ONLY)Duration = 12 + months* *Local candidates are HIGHLY preferred* *The scope of work to be performed includes but is not limited to the following: *Review of Functional Specifications and Design Specifications Review of vendor FAT/DT to include all process failure paths, sequence of operations, graphics, and navigation Review of FAT/DT/SAT to include parameter settings verification and connectivity verification Review of protocols for standard sequence of operations, standard graphics, standard alarms, and non-standard infrastructure Develop, execute and close Automation and EBM protocols. *The resource needs to have knowledge in Automation systems (BAS /DHS/PCS) and in EBM.* • In depth knowledge of computerized life cycle development processes involving various types of systems: Emerson DeltaV, Siemens Simatic IT eBR,, Building Automation Systems (BAS) (specific, Honeywell EBI), Environmental Monitoring Systems (EMS), and Plant Information and Data Acquisition Systems (PI). •Demonstrated experience generating and executing integrated commissioning and qualification documents for the listed platforms preferred. • Execution knowledge of automation in Purification, Utilities, Fill / Finish desirable • Demonstrated experience generating change control plans and computer validation assessment for the control systems to maintain the validated state during the system lifecycle. • Participate in Root Cause Analysis exercises for deviations/CAPA investigations. • Demonstrated experience generating and executing qualification of PLCs, SQL Servers, Software applications (Rockwell RSBatch, Rockwell RSLogix, Rockwell RSView, and SCADA). • Experience in developing and implementing Computer Validation policies and procedures including training material and life cycle management-processes. • Knowledge of cGMPs for Pharmaceuticals and Quality Systems: 21 CFR Part 210, 211 and 820. ____________________________________________________________________________________________________________________________________________________________________________ Thanks & Regards, James Miller Sr. IT Recruiter | ITBrainiac Inc, Princeton Forrestal Village116 Village Blvd, Suite 200 Princeton, NJ 08540 Tel 609 - 423 - 4899 Fax 312.582.2699 | Email:[email protected] Gtalk: james.usrecruiter Website: www.itbrainiac.com “I can do all things through Christ who strengthens me”- Philippians 4:13 Notice: This email contains confidential or proprietary information which may be legally privileged. It is intended only for the named recipient (s). If an addressing or transmission error has misdirected the email, please notify the author by replying to this message by "REMOVE". If you are not the named recipient, you are not authorized to use, disclose, distribute, copy, print or rely on this email, and should immediately delete it from your computer system. it from your computer system.
