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ICONMA, LLC

Sr. Manufacturing Automation Engineer DeltaV / Allen-Bradley

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What they do

A Manufacturing Automation Engineer designs, programs and improves automated machinery and processes within a manufacturing environment. Are responsible for the design specifications, documentation and troubleshooting of the equipment. Often work within vehicle manufacturing and food processing plants, where robots or machines are used to perform specific functions.

$100,718 / year median in Pennsylvania

+10% projected growth

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Job Description

Sr. Manufacturing Automation Engineer - DeltaV / Allen-Bradley#26-34835

$48.57-$53.57 per hour

West Point, PA

Onsite

Job 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