Automation Validation Engineer

JSat Automation

$70K — $95K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Minimum BS Degree in Engineering (Computer Science, Electronics, Electrical, Chemical, etc.)
  • 0 to 7 months experience in the process industry
  • Familiarity with Control Systems (Emerson DeltaV, Allen Bradley, Foxboro, Siemens, Honeywell)
  • Experience with SCADA, MES, and database systems a plus
  • Knowledge of computer system validation is advantageous

Responsibilities

  • Design and develop manufacturing control systems to support process operations
  • Interact with clients to identify and analyze automation improvement opportunities
  • Create validation documents in accordance with FDA cGMP and GAMP standards
  • Program, test and validate automation systems for process control
  • Prepare and execute validation protocols for 21 CFR Part 11 compliance
  • Manage and document system upgrades through change control procedures
  • Troubleshoot and resolve issues with field control systems

Benefits

  • Up to 40% travel to client sites
  • Opportunity to work on diverse automation projects
  • Exposure to industry-standard tools and technologies
  • Professional development opportunities
  • Hands-on experience in a fast-paced environment
Full Job Description
Job Description
JSat Automation is hiring an Automation Validation Engineer for their Blue Bell Office. This position is up cowith up to 40% travel to client sites.

This Engineer will be responsible for the following
  • Design and develop manufacturing control systems in support of process operations.
  • Interact with client personnel to identify and analyze continuous improvement through automation upgrades.
  • Develop validation documents per FDA cGMP and GAMP standards, functional specifications, design specifications and requirements trace matrices.
  • Design, program, test and validate process control automation systems.
  • Prepare and execute validation protocols (AIQ, IQ, OQ) for 21 CFR Part 11 compliance per FDA requirements
  • Manage, document, and implement these upgrades through changes control procedures.
  • Execute capital projects including but not limited to:
  • Control system software development
  • Control system hardware design
  • Network design
  • MES system implementation
  • Recipe management
  • User requirement specification development
  • Process equipment installations.
  • SOP development and training on Automation Systems.
  • Troubleshoot, analyze, and resolve field control system issues.
  • Develop, review, and / or execute automation qualification and validation protocols.
  • Design, develop, and implement technical solutions by establishing integration strategies, configuring and programming PLCs, DCSs as well as design, build, install and integrate automation control system hardware, panels and field devices.
  • Up to 40% travel to client sites


Requirements

  • We require a minimum BS Degree in Engineering (Computer Science, Electronics, Electrical, Chemical, etc.) or equivalent with 0 to 7 months experience in process industry.
  • Experience in Control Systems (Emerson DeltaV, Allen Bradley, Foxboro, Siemens, Honeywell). Experience with SCADA, MES, and database systems, or computer system validation are considered a plus.

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