Senior Automation Engineer (PLC)
@ Long Finch TechnologiesSenior Automation Engineer (PLC)
About the job
Supports manufacturing and quality by designing, troubleshooting, and maintaining automation systems like PLCs and SCADA. Ensures compliance and collaborates with stakeholders in a biotech or manufacturing environment. W2/H1 considered.
Requirements
- DeltaV and PLC troubleshooting
- GMP industry understanding
- Strong communication skills
- Experience with validation deliverables
- Interface integration knowledge
Qualifications
- Experience with biotech or pharma
- Understanding of regulatory standards
- Work with control systems
Full job description
ALL US VISA's ARE ACCEPTED
W2 ROLE (H1 TRANSFERS ARE ACCEPTED)
Job Description-
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
Top 3 skills required for this role-
1. DeltaV and PLC ( Allen-Bradley/ Rockwell ) Configuration and Troubleshooting Experience
2. Life Sciences industry understanding of GMP concepts: data integrity (ALCOA+), electronic signatures, validation requirements, audit trails, controlled documents, deviations/CAPA, and change control
3. Strong Communication and Interpersonal skills to collaborate with diverse stakeholders and drive decisions
Additional Information-
- 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.
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