Staff Automation Engineer, CSV

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com . As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit. Job Function: Supply Chain Engineering Job Sub Function: Automation Engineering Job Category: Scientific/Technology All Job Posting Locations: Anasco, Puerto Rico, United States of America Job Description: About Vision Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments. Are you passionate about improving and expanding on the possibilities of vision treatments? Ready to join a team that’s reimagining how vision is improved? Our Vision team solves the toughest health challenges. Help combine cutting-edge insights, science, technology, and people to encourage eye care professionals and patients to proactively protect, correct and enhance healthy sight for life. Our products and services address these needs – from the pediatric to aging eye – in a patient’s lifetime. Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech We are searching for the best talent for Staff Automation Engineer, CSV. Purpose: We are seeking a highly experienced Staff Automation Engineer, CSV to serve as the technical authority for Computer System Validation (CSV) across automated manufacturing systems. This role is responsible for establishing, executing, and sustaining cGMP compliant automation system lifecycle practices in support of new product introductions, system upgrades, and operational excellence initiatives. The position combines deep automation systems knowledge with full ownership of CSV strategy, validation execution, and regulatory alignment. The successful candidate will act as a technical leader and primary interface with Quality, IT, and Regulatory partners, ensuring all automated systems meet FDA, cGMP, and data integrity requirements. You will be responsible for: CSV & System Lifecycle Leadership Serve as CSV technical lead for automated manufacturing systems, infrastructure, and services Define and execute validation strategies for PLC, SCADA, MES-adjacent, historian, and infrastructure systems Own the full system lifecycle from concept through decommissioning in alignment with GAMP and J&J standards Lead risk-based validation approaches including system impact assessments, risk assessments, and mitigation strategies Ensure complete traceability between URS, FRS, DS, IQ, OQ, PQ, and RTM documentation Act as SME during internal and external regulatory audits supporting FDA, notified bodies, and corporate assessments Systems Management & Automation Leadership Lead the management of existing equipment and control systems across assigned manufacturing areas Resolve complex reliability issues and conduct assessments for system modernization needs Implement automation requirements with full accountability for scheduling, resource management, maintenance, and operational support Conduct comprehensive regulatory compliance assessments and implement improvements to meet cGMP, FDA, and other regulatory requirements GMP / GxP Compliance & Regulatory Readiness Ensure compliance with cGMP, GxP, and FDA regulations for automated systems Lead implementation and assessment of 21 CFR Part 11 controls including audit trails, security, data integrity, and electronic signatures Drive adherence to change control, deviation, CAPA, and periodic review processes for validated systems Partner with Quality to define and implement validation governance and SOPs Perform periodic system reviews to ensure continued validated state and regulatory readiness HMI/SCADA Development & Control Systems Design, build, and implement HMI applications using industry-standard platforms including Ignition, Wonderware, iFIX, FactoryTalk View, and FactoryTalk Optix Create intuitive user interfaces with optimized layout design, navigation functionality, and operator-friendly screen development Design and implement comprehensive automation systems including robotics integration, advanced PLC programming, and sophisticated control system architectures Integrate multiple subsystems while optimizing performance and ensuring seamless operational flow Technical Problem Resolution & System Integration Diagnose and resolve complex technical issues involving both software and hardware components of automated equipment Lead solving efforts for critical production systems and implement preventive maintenance strategies Provide on-call support for production operations as needed Handle system integrations across diverse platforms including Beckhoff, Allen-Bradley, Siemens, Wonderware, and data historian systems Project Leadership & multi-functional Collaboration Lead small to medium-sized multidisciplinary teams including Computer System Validation (CSV) specialists, IT professionals, and various engineering fields Apply Microsoft Project for comprehensive project planning, resource allocation, timeline management, and budget control Conduct technical design reviews and vendor management meetings with equipment suppliers and service providers Prepare detailed Standard Operating Procedures (SOPs), work instructions, and user documentation Manage Computer System Validation (CSV) processes and system lifecycle documentation throughout project phases Qualifications / Requirements: Experience & Education Minimum of a Bachelor's degree in an Engineering, Automation, Robotics, Computer Science or Software Engineering fields with over 4 years’ experience working with automated controls systems in a highly automated, regulated manufacturing environment is required. GMP Environment Experience: Extensive working knowledge in regulated pharmaceutical or medical device manufacturing operations Team Leadership: Proven tra