Staff Automation Engineer, Csv

Johnson & Johnson Johnson & Johnson · Pharma · Anasco, Puerto Rico +1

Staff Automation Engineer, CSV responsible for establishing, executing, and sustaining cGMP compliant automation system lifecycle practices for automated manufacturing systems, ensuring compliance with FDA, cGMP, and data integrity requirements. This role involves leading CSV strategy, validation execution, and regulatory alignment, acting as a technical leader and interface with Quality, IT, and Regulatory partners.

What you'd actually do

  1. Serve as CSV technical lead for automated manufacturing systems, infrastructure, and services
  2. Define and execute validation strategies for PLC, SCADA, MES-adjacent, historian, and infrastructure systems
  3. Own the full system lifecycle from concept through decommissioning in alignment with GAMP and J&J standards
  4. Lead risk-based validation approaches including system impact assessments, risk assessments, and mitigation strategies
  5. Ensure complete traceability between URS, FRS, DS, IQ, OQ, PQ, and RTM documentation

Skills

Required

  • Computer System Validation (CSV)
  • Automation systems
  • cGMP compliance
  • FDA regulations
  • PLC programming
  • SCADA systems
  • MES systems
  • HMI development (Ignition, Wonderware, iFIX, FactoryTalk View, FactoryTalk Optix)
  • Robotics integration
  • Beckhoff
  • Allen-Bradley
  • Siemens
  • Risk assessment
  • Change control
  • Deviation management
  • CAPA
  • Project management (Microsoft Project)

Nice to have

  • System modernization
  • Operational excellence
  • Data integrity controls
  • Electronic signatures
  • Periodic system reviews

What the JD emphasized

  • cGMP
  • FDA
  • data integrity
  • 21 CFR Part 11
  • validated state