Senior Automation Engineer (PLC)
@ Long Finch TechnologiesSenior Automation Engineer (PLC)
About the job
We are a biotech focused on biologics and cell therapy. The Senior Automation Engineer supports automation systems, ensures compliance, and collaborates with project teams in a regulated environment.
Requirements
- DeltaV and PLC troubleshooting
- GMP and biotech industry knowledge
- Communication skills
- Experience with validation deliverables
- Interface and integration knowledge
Qualifications
- Biotech or life sciences background
- Understanding of GMP concepts
- Experience in sterile manufacturing
- Familiarity with validation procedures
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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