Automation Engineer - Validation
Duration: 12-18 Months with possible extension ON-SITE
Location: Ridgefield Park, NJ 07660 POSITION DESCRIPTION:
Essential Functions of the job:
Responsible for P&ID review, Electrical design, and Drawings review, prepare I/O Lists, provide technical support to OEM Engineers, facilitation of systems integration.
Support validation during SAT/IQ/OQ
Execute Test Protocols, Exception resolution and change controls.
Assist with System backup, User Group creation.
Training
As built documentation Core Competencies, Knowledge, and Skill Requirements
Experience working in a FDA-regulated biotechnology or pharmaceutical company
Experience in Automation, Electrical controls systems, instrumentation, and CSV
Experience in equipment qualification and process validation, Supporting Greenfield Pharma plant startup.
Experienced in Upstream and Downstream manufacturing processes in biopharmaceutical such as Filtration systems, Bioreactors, CIP, SIP, WFI system, Buffer Prep, Autoclaves and Biowaste systems. Strong communication skills (written and verbal).
Experience using Studio 5000 Logix Designer, FTView SE & ME, , FTAssetCentre, WIN911 FTBatch, and PlantPAX / Delta-V
Experience using TIA Portal and WinCC
Rockwell / Siemens PLC, Drives
OPC DA and UA Communication, OSI PI / Bio Reactors is desirable.
Strong analytical and problem-solving ability.
Hands-on approach, with a 'can do' attitude.
Ability to prioritize, demonstrating good time management skills.
Employment Type: Contractor
Salary: $ 55.00 Per Hour
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