Senior Automation Engineer - Control

Johnson & Johnson Innovative Medicine

Anasco, Puerto Rico, United States
On-site
Plc and scada solutions
Cgmp, fda, and 21 cfr part 11 compliance
Allen-bradley, siemens, and beckhoff systems
Johnson & Johnson is seeking a Senior Automation Engineer - Control to manage and enhance automation systems in a regulated manufacturing environment, particularly in the vision care sector. The role involves overseeing control systems, ensuring regulatory compliance, and collaborating with cross-functional teams to drive innovation

Job Summary

  • Administers automation and control systems for both modernized and legacy systems, infrastructure, and services.
  • Designs and implements high-quality PLC and SCADA solutions from functional and detailed design specifications, supporting all phases of lifecycle including validation in validated manufacturing environments compliant with cGMP, FDA, and 21 CFR Part 11.
  • Provides technical guidance and mentorship to junior engineers and consistently applies Johnson & Johnson’s Credo and Leadership Imperatives in day-to-day interactions.

Matching Summary

Match Score: 85

Johnson & Johnson is seeking a Senior Automation Engineer - Control to manage and enhance automation systems in a regulated manufacturing environment, particularly in the vision care sector. The role involves overseeing control systems, ensuring regulatory compliance, and collaborating with cross-functional teams to drive innovation.

Skills & Requirements

Must-have

  • PLC and SCADA solutions
  • cGMP, FDA, and 21 CFR Part 11 compliance
  • Allen-Bradley, Siemens, and Beckhoff systems
  • Computer System Validation (CSV) methodologies
  • IEC 61131 and IEC 61508 standards

Nice-to-have

  • Industry 4.0 initiatives
  • Cloud-based automation solutions
  • Artificial Intelligence integration
  • Advanced process analytics
  • Redundancy configurations

Key Requirements

  • Bachelor's degree in engineering
  • 2+ years of experience in automated controls
  • Proficiency in Allen-Bradley, Siemens, and Beckhoff
  • Knowledge of cGMP regulations and FDA requirements
  • Experience with qualification protocols (IQ/OQ/PQ)

Work Rights

Not specified

Tailored Resume

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