Sr. Manufacturing Automation Engineer - DeltaV / Allen-Bradley

Iconma LLC

  • West Point, PA
  • 12 days ago

    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

    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?

    • Health Benefits
    • Referral Program
    • Excellent growth and advancement opportunities

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