Senior Siemens S7 PLC Engineer
United Pharma
Job Description
Job Summary
\nWe are seeking an experienced Siemens S7 PLC Engineer to support a major pharmaceutical/biopharmaceutical project in Holly Springs, NC . The consultant will provide hands-on PLC programming, troubleshooting, commissioning, and automation support within a regulated manufacturing environment.
\nThe ideal candidate will have strong experience working with Siemens S7 PLC platforms , industrial automation systems, HMI/SCADA, controls troubleshooting, and equipment integration. Experience in pharmaceutical, biotechnology, life sciences, or other GMP-regulated manufacturing environments is highly preferred.
\nThis is a long-term onsite contract of approximately 10 months , and candidates must be available to start within 2–3 weeks .
\nKey Responsibilities
\n- \n
- Develop, modify, troubleshoot, and maintain Siemens S7 PLC control programs . \n
- Support PLC programming and automation activities throughout the project lifecycle. \n
- Troubleshoot PLC, HMI, instrumentation, and control-system issues in a manufacturing environment. \n
- Perform PLC code reviews, logic modifications, testing, and debugging. \n
- Support equipment integration and communication between PLCs, HMIs, SCADA systems, and other automation platforms. \n
- Participate in commissioning, startup, testing, and site acceptance activities . \n
- Execute and support FAT, SAT, commissioning, and qualification-related activities as required. \n
- Review control-system specifications, functional requirements, and automation documentation. \n
- Develop or modify PLC logic, sequences, interlocks, alarms, permissives, and control strategies. \n
- Troubleshoot industrial communication networks and PLC-to-device communications. \n
- Support HMI development, modifications, alarm configuration, and operator-interface functionality. \n
- Collaborate with electrical, instrumentation, process, engineering, validation, and manufacturing teams. \n
- Document automation changes, testing activities, troubleshooting results, and system updates. \n
- Ensure automation activities are performed in accordance with applicable GMP, safety, quality, and site procedures . \n
- Provide onsite support during equipment installation, commissioning, startup, and production readiness. \n
- Assist with resolving automation issues and minimizing equipment downtime. \n
- Participate in project meetings and provide technical updates to project leadership. \n
Required Qualifications
\n- \n
- Bachelor's degree in Electrical Engineering, Controls Engineering, Automation Engineering, Computer Engineering , or a related technical discipline; equivalent experience may be considered. \n
- Strong hands-on experience with Siemens S7 PLCs . \n
- Experience with Siemens TIA Portal and/or STEP 7 . \n
- Strong understanding of PLC programming, troubleshooting, sequencing, interlocks, alarms, and controls logic. \n
- Experience with HMI/SCADA systems and industrial automation. \n
- Experience with industrial communication protocols and PLC/device integration. \n
- Hands-on experience with commissioning, startup, troubleshooting, and system testing. \n
- Ability to read and interpret electrical schematics, control drawings, I/O lists, and automation documentation. \n
- Strong troubleshooting and problem-solving skills. \n
- Excellent communication and documentation skills. \n
- Ability to work effectively in a fully onsite project environment . \n
Preferred Qualifications
\n- \n
- Experience in pharmaceutical, biotechnology, medical device, or other GMP-regulated manufacturing environments . \n
- Experience supporting automation projects from design through commissioning and startup. \n
- Experience with Siemens WinCC, PCS 7, or related Siemens automation platforms . \n
- Experience with Rockwell/Allen-Bradley PLCs in addition to Siemens. \n
- Knowledge of industrial networking, including Ethernet/IP, Profinet, Profibus, or similar protocols. \n
- Experience with manufacturing equipment integration. \n
- Familiarity with GAMP 5, 21 CFR Part 11, data integrity, and computerized system validation (CSV) concepts. \n
- Experience supporting FAT/SAT and validation documentation in regulated environments. \n
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