Delta V Automation Engineer

At KAPS Automation, we deliver innovation through Automation Systems and Digitization Technology for enhanced operational efficiency and data‑driven decision‑making of Industrial Operations for Life Sciences Manufacturing Clients globally. We are experts in Pharma 4.0 and Digitalization for Life science Industry, ensure GxP compliance, and enhance operational efficiency. With a strong presence across USA and India we specialize in end‑to‑end implementation and support of GMP manufacturing systems and solutions, Automation, Manufacturing Execution Systems (MES), IT/OT Networking, AVEVA PI, LIMS Systems and other Digital Technologies.

We will only consider candidates who have existing Employment Valid Visa and do not need sponsorship from us.

• This is 100% on site with our Life science Client
• Maintain and support facility automation and control systems to ensure safe, compliant, and reliable operations aligned with cGMP, data integrity, and regulatory requirements.
• Provide automation support for manufacturing and pilot plant processes, including real‑time troubleshooting, system monitoring, and efficiency improvements.
• Participate in capital project execution — design, implementation, startup, commissioning, qualification, and documentation for new automation systems and equipment upgrades.
• Work collaboratively with Process Engineering, Manufacturing, Facilities, IT, QA, and OEM vendor partners to resolve automation issues and implement continuous improvement initiatives.
• Configure, test, and maintain automation software/hardware including DCS, PLCs, SCADA, and batch systems.
• Support change control processes: author, review, and execute SDLC/CSV deliverables, including URS, FRS, FAT/SAT, IQ/OQ, and system drawings.
• Perform system administration tasks including backups, user access, patching, asset lifecycle management, and data integrity controls.
• Participate in deviations, QNs, and CAPA development and ensure timely closure of automation‑related quality records.
• Document technical activities clearly and accurately in compliance with cGMP and internal site procedures.
• Promote improvement of automation reliability and performance through proactive maintenance, data analysis, and technology modernization.

• Bachelor’s degree in Instrumentation or electrical engineering, Computer Science, Chemical Engineering, or related discipline.
• (Equivalent technical experience may be considered for the right candidate.)

• 3–7+ years of hands‑on automation or process control experience in a GMP manufacturing environment.
• Experience configuring and troubleshooting one or more of the following:
• Batch control aligned with ISA‑88 / ISA‑95
• Strong understanding of control logic, instrumentation, networks, and system architecture.
• Practical experience with change controls, validation, and computerized system lifecycle (CSV/SDLC).
• Ability to support rotating on‑call and respond to urgent system events during manufacturing operations.
• Excellent problem‑solving and communication skills; able to work both independently and in cross‑functional teams.
• Commitment to personal/workplace safety and adherence to quality standards.

• Experience supporting biopharmaceutical Bulk Drug Substance, vaccine, or single‑use manufacturing systems.
• Knowledge of MES integration, PI/Data Historians, virtualization, OT‑IT networking, and cybersecurity fundamentals.
• Ability to manage small automation improvement projects, including scope, schedule, and vendor coordination.
• Experience supporting regulatory audits and inspections.

Mid‑Senior level

Full‑time

Engineering and Information Technology

IT Services and IT Consulting, Automation Machinery Manufacturing, and Pharmaceutical Manufacturing

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401(k)

San Diego, CA $-$