37 минут назад
Senior Automation Engineer (Controls)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Senior Automation Engineer (Controls) (MedTech manufacturing automation): Designing, validating, and maintaining PLC, SCADA, robotics, safety, motion, vision, and integrated control systems for regulated manufacturing environments with an accent on system reliability, compliance, and lifecycle modernization. Focus on solving complex automation and hardware issues, leading IQ/OQ/PQ validation, integrating Beckhoff, Allen-Bradley, Siemens, and Wonderware platforms, and supporting production operations.
Location: Anasco, Puerto Rico, United States of America; onsite
Company
Johnson & Johnson MedTech develops healthcare and vision solutions that combine medical science, technology, and innovation.
What you will do
- Develop, install, maintain, and modernize automated control systems covering PLCs, safety PLCs, robotics, electrical systems, servo motion, machine vision, SCADA, and device integration.
- Design and implement PLC and SCADA solutions for new and legacy equipment in validated manufacturing environments.
- Lead or support equipment procurement, installation, qualification, validation, risk assessments, and safety design reviews.
- Diagnose complex software and hardware issues, support critical production systems, and provide on-call assistance when required.
- Integrate Beckhoff, Allen-Bradley, Siemens, Wonderware, databases, and data historian systems.
- Prepare project plans, SOPs, work instructions, validation documentation, and lifecycle records while coordinating with vendors and cross-functional teams.
Requirements
- Bachelor’s degree in engineering is required; automation, robotics, computer science, or an equivalent degree is preferred.
- At least 2 years of experience with automated control systems in regulated, highly automated manufacturing environments.
- Proficiency with Allen-Bradley PLC families, Siemens S7 systems, and Beckhoff TwinCAT.
- Experience with operator interfaces, databases, reporting systems, data collection platforms, computer system validation, and system lifecycle management.
- Knowledge of cGMP, FDA requirements, IQ/OQ/PQ qualification, ISO 13485, ISO 9001, IEC 61508, IEC 61511, ISO 12100, and 21 CFR Part 11.
- Ability to work in a fast-paced manufacturing environment, support production operations during off-hours, and produce technical documentation.
Nice to have
- Experience with Ethernet/IP, Profinet, Modbus, managed switches, VLANs, and industrial wireless systems.
- PE license or Beckhoff, Rockwell Automation, or Siemens certifications.
- Experience with Industry 4.0, cloud automation, data analytics, machine learning, artificial intelligence in manufacturing, backup systems, redundancy, or disaster recovery.
Culture & Benefits
- Work within a healthcare and vision technology organization focused on developing smarter and less invasive treatments.
- Collaborate with internal and external subject matter experts, project managers, equipment suppliers, and service providers.
- Contribute to an inclusive work environment that values individual dignity, diversity, and merit.
- Support company initiatives, KPI achievement, regulatory compliance, and continuous improvement in manufacturing operations.
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