Electrical Automation Engineer

  • by
Location
Candidate No.
1710047

About this Candidate

DAVRON CV: Candidate 1710047

SENIOR AUTOMATION ENGINEER & PROJECT MANAGER | PHARMA GMP | PLC/HMI | VALIDATION & COMMISSIONING

Core Expertise

  • Leading automation and controls programs for FDA/GMP-regulated pharmaceutical manufacturing and sterile filling operations.
  • Managing CAPEX projects from concept through commissioning, including equipment modernization and line installations.
  • Developing validation artifacts (URS, FRS, IQ/OQ) and executing compliant commissioning and qualification.
  • Driving continuous improvement and reliability initiatives that reduced downtime and operating costs.
  • Leading cross-functional teams, vendor management, and stakeholder communication for complex projects.

Project Background

  • Upgraded legacy control systems and modernized PLC/HMI architectures to improve maintainability.
  • Implemented serialization and track & trace integrations with packaging lines and MES systems.
  • Executed equipment installations and full lifecycle commissioning for sterile filling and packaging assets.
  • Authored URS/FRS and managed IQ/OQ protocols ensuring regulatory compliance and audit readiness.
  • Delivered continuous improvement projects improving overall equipment effectiveness and cross-site performance.

Key Skills

  • PLC & HMI Controls | Allen-Bradley | Siemens | Beckhoff
  • SCADA & Historian | Wonderware | Intellution | PI Historian
  • MES Integration | Serialization | Track & Trace
  • Validation & Compliance | URS | FRS | IQ/OQ | 21 CFR Part 11 familiarity
  • Commissioning & Startup | FAT/SAT | Troubleshooting | Equipment Qualification
  • Project & CAPEX Management | Budgeting | Vendor Coordination | Cross-functional Leadership
  • Continuous Improvement | Root Cause Analysis | OEE & Reliability Improvements

Education

  • Automation Technologies — St. Louis County Technical School

Why Interview this Candidate?

The candidate brings over two decades of hands-on automation and project leadership in GMP-regulated pharmaceutical environments. Proven ability to modernize controls, lead validation and commissioning, and integrate MES/serialization to improve reliability and compliance. Strong track record managing CAPEX, vendors, and cross-functional teams to deliver measurable OEE and cost improvements.

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