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Lonza

Senior Biopharmaceutical Manufacturing Automation Engineer

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Job Description

Senior Biopharmaceutical Manufacturing Automation Engineer Date Posted:
26 September 2026
Closing Date:
October 26, 2026
Recruiter:
Lonza Location:
Bend, Oregon Salary:
USD125,000
to
USD155,000
Job Type & Industry:
Data, Ai & Technology >
Ai & Technology Governance, Technology Risk, Production, Manufacturing & Operations Contract Type:
Permanent Job Reference:
2988837754-2 Apply for this job now Job Description Lonza is seeking an experienced Automation Engineer to design, implement, and support advanced automation for biopharmaceutical manufacturing. In this role you will develop and optimize PLC/SCADA and DCS-based systems in a GMP environment, ensuring reliability, data integrity, and regulatory compliance. You will collaborate with cross-functional teams on technology transfer, troubleshooting, and continuous improvement, while supporting commissioning, qualification, and lifecycle management. This position offers exposure to cutting-edge bioprocess technologies, global projects, and strong opportunities for professional growth in a mission-driven, patient-focused organization. Responsibilities Design, implement, and optimize automation solutions for biopharmaceutical manufacturing processes Develop, configure, and maintain PLC/SCADA and DCS systems in a GMP-regulated environment Collaborate with process engineering, QA, and operations to ensure reliable and compliant automation performance Lead troubleshooting, root-cause analysis, and continuous improvement of automated systems Author and maintain technical documentation, URS, FDS, test plans, and validation protocols Support system commissioning, qualification, and lifecycle management for new and existing equipment Ensure data integrity, cybersecurity, and integration with MES and data historians Provide on-call and shop-floor support to maintain high equipment uptime Contribute to technology transfer and scale-up activities across global Lonza sites Mentor junior engineers and share best practices in automation and control technologies Required Skills PLC programming (Rockwell, Siemens, or similar)
SCADA/HMI
configuration and support DCS systems in GMP manufacturing GAMP 5 and computer system validation (CSV)21 CFR Part 11 and data integrity compliance GMP biopharma process automation (upstream/downstream/fill-finish) Industrial networking and control system cybersecurity Batch control (ISA-88) and recipe management MES integration and data historians Root cause analysis and continuous improvement (Lean/Six Sigma)

Benefits

  • Professional Development