Hope you are doing well.
We have an immediate opening for Validation Technician Please go through the below requirement and send me your updated resume to akil@globalpharmatek.com or please call me on 732- 228-4115 to discuss more about this position.
Title : Validation Technician
Location : IL
Duration : 6+ Months
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,
Akil R
15 Corporate Place S, Suite 345, Piscataway, New Jersey - 08854
US Tel : 732-543-7155 Ext.: 9055 | US Direct: 732- 228-4115 | Fax : 732-474-0144
akil@globalpharmatek.com | www.globalpharmatek.com
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