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Sr. Manufacturing Automation Engineer DeltaV / Allen-Bradley

ICONMA, LLC

  • West Point, PA
  • 8 days ago
  • $48.57–$53.57 Per Hour

Highlights

Responsibilities: Senior Automation Engineer is responsible for supporting manufacturing business, project team and Quality in designing / configuring / updating / troubleshooting / documenting Automation systems. Life Sciences industry understanding of GMP concepts: data integrity (ALCOA+), electronic signatures, validation requirements, audit trails, controlled documents, deviations/CAPA, and change control.

Numbers & Facts

LocationWest Point, PA
Salary$48.57–$53.57 Per Hour

Description

Our client, a IT Services and Consulting company, is looking for a Sr. Manufacturing Automation Engineer – DeltaV / Allen-Bradley for their West Point, PA location.
 
Responsibilities:
  • Senior Automation Engineer is responsible for supporting manufacturing business, project team and Quality in designing / configuring / updating / troubleshooting / documenting Automation systems
  • Design, configure, and maintain PLCs (Allen-Bradley/Rockwell), SCADA, DeltaV system.
  • Troubleshoot, maintain, and upgrade existing control systems.
  • Provide technical support to customers, engineers, and other stakeholders during PPQ phase.
  • Draft / Update relevant URS/FRS/DS/Test Protocols as part of implementation or qualification process
  • Monitor and analyze system performance.
  • Ensure regulatory compliance with safety, environmental and quality standards.
  • Utilize best practices, standards and procedures related to automation systems maintenance.
  • Handle Change Control related processes and technical documentation, including design specification, user manuals, and operational procedures in.
  • Participate in project management and project coordination.
  • Support interfaces between Data Historians, Control Systems, MES
 
Requirements:
  • DeltaV and PLC ( Allen-Bradley/ Rockwell ) Configuration and Troubleshooting Experience
  • Life Sciences industry understanding of GMP concepts: data integrity (ALCOA+), electronic signatures, validation requirements, audit trails, controlled documents, deviations/CAPA, and change control
  • Strong Communication and Interpersonal skills to collaborate with diverse stakeholders and drive decisions
  • Team size, direct reports, key deliverables, unique selling points, additional qualifications, team culture etc.
  • Experience with sterile manufacturing, biologics, cell therapy, or fill-finish operations.
  • Exposure to interfaces/integration concepts (ERP/LIMS/SCADA), ISA-88/ISA-95, and master data governance.
  • Experience supporting or authoring validation deliverables (URS/FS/DS, IQ/OQ/PQ) for Automation changes.
  • 12.00 Years of Experience
 
Why Should You Apply?

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