Automation Technitian

JC Automation, Corp.; Carolina (PR); On-site; USD 55,000 - 75,000; Full time

Job summary

JC Automation Corp. is seeking two Automation Technicians to support automation and control systems in a cGMP pharmaceutical environment. You will diagnose, repair, and maintain PLCs, SCADA, and DCS, while ensuring data integrity and regulatory compliance.

Night shift coverage may be required, with on-site responsibilities and a focus on safety and quality. The role involves incident response, preventive maintenance, validation support, CAPA activities, and collaboration with Automation

Qualifications

• Bachelor's or Associate's degree in Electrical, Electronic, Computer Engineering, Industrial Technology, or related technical discipline.
• 2–4 years hands-on experience with industrial automation systems (PLCs, SCADA, DCS) in manufacturing or pharmaceutical environments.
• Troubleshooting and resolving automation incidents independently.
• Familiarity with cGMP, data integrity, and change control processes.
• Preventive maintenance execution and documentation.
• Bilingual in English and Spanish (oral and written).

Responsibilities

• Diagnose and resolve incidents related to PLCs, SCADA, DCS, and networked manufacturing equipment to minimize production impact.
• Provide onsite coverage during assigned shift hours, including overnight as required.
• Perform root cause analysis for automation incidents and support CAPA development.
• Execute and document preventive maintenance plans in CMMS.
• Support automation project tasks, system upgrades, and validation activities under supervision.
• Assist in validation protocol execution, CSV documentation, and findings resolution.
• Provide shift turnover communications and documentation of system status, incidents, actions, and follow-ups.
• Ensure compliance with cGMP, safety, cybersecurity, data integrity, and quality practices.

Job description

JC Automation Corp. (JCA) was founded in 1997 with the mission of filling a gap between technology and regulatory requirements in the life science manufacturing industry. The company offers highly capable resources at an affordable cost to build solutions and execute projects in: Automation, Control Systems Integration, Information Technology, System Integration and Regulatory Compliance.

JCA is a HUBZone Certified Small Business Firm, NMSDC Certified Minority Business Enterprise, and Certified Critical Industry Supplier. It’s mission is to add value by delivering quality services & solutions on time all the time by transforming processes & technology into business advantages.

ABOUT THE ROLE

We are seeking two skilled Automation Technicians to provide hands-on technical support for automation and control systems. In these roles, you will ensure the continuous operation and reliability of manufacturing and utilities automation systems, including PLCs, SCADA, DCS, and networked manufacturing equipment, within a cGMP pharmaceutical environment.

You will work as part of the site automation team, responding to incidents, executing preventive maintenance plans, supporting validation activities, and ensuring full compliance with cGMP, data integrity, and applicable Quality Practices. Night shift coverage may be required based on operational needs.

RESPONSIBILITIES

• Incident Diagnosis & Resolution:Diagnose and resolve incidents related to PLCs, SCADA, DCS, and networked manufacturing equipment, ensuring rapid response to alarms and system faults to minimize production impact.
• Overnight Operations Coverage:Provide onsite coverage during assigned shift hours (including overnight as required), ensuring rapid and effective response to system alarms, equipment failures, and automation issues.
• Root Cause Analysis & CAPA:Perform root cause analysis for automation incidents, support corrective and preventive action (CAPA) development, and coordinate or perform component replacements as needed.
• Preventive Maintenance Execution:Execute and maintain the automation preventive maintenance agenda, ensuring scheduled tasks are completed accurately, on time, and fully documented in the CMMS.
• Project & Upgrade Support:Support automation project tasks, system upgrades, and improvements under the supervision of the Automation Engineer or Technical Lead, in alignment with applicable Quality Practices and Engineering standards.
• Validation Support:Assist in the execution of validation protocols, testing activities, CSV documentation authoring, and resolution of findings related to automation systems.
• Shift Reporting & Handover:Provide structured shift turnover communication and documentation including system status, incidents, corrective actions, PM execution, and pending follow-up items.
• Compliance & Safety:Ensure all activities comply with cGMP, safety protocols, cybersecurity requirements, data integrity standards, training plans, and applicable Quality Practices.

REQUIREMENTS & QUALIFICATIONS

Required

• Associate's or Bachelor's degree in Electrical, Electronic, Computer Engineering, Industrial Technology, or a related technical discipline.
• Minimum 2–4 years of hands-on experience with industrial automation systems (PLCs, SCADA, DCS) in a manufacturing or pharmaceutical environment.
• Demonstrated ability to troubleshoot and resolve automation incidents independently.
• Familiarity with cGMP standards, data integrity requirements, and change control processes.
• Ability to execute preventive maintenance plans and document activities accurately.
• Bilingual in English and Spanish (oral and written).

Preferred

• Experience with Rockwell Automation (ControlLogix, CompactLogix) or Siemens PLC platforms.
• Exposure to Computer System Validation (CSV) activities and documentation.
• Familiarity with OSI PI historian or equivalent data contextualization platforms.
• Prior experience in a pharmaceutical, biotech, or FDA-regulated manufacturing environment.
• Knowledge of Kneat Software or equivalent validation management tools.

SKILLS

Technical Skills

• PLCs, HMIs, SCADA, DCS systems — hands-on troubleshooting and maintenance
• Automation preventive maintenance execution and CMMS documentation
• Root cause analysis and CAPA support
• cGMP, data integrity, and safety compliance fundamentals
• CSV validation support — protocol execution and documentation
• Shift reporting and handover documentation
• Microsoft Office 365 — Word, Excel, Teams

Soft Skills

• Reliable and responsive — able to act quickly and decisively during operational incidents
• Detail-oriented with strong documentation discipline
• Self-driven and accountable for completing assigned tasks independently
• Collaborative team player who communicates clearly during shift transitions
• Committed to safety, quality, and continuous improvement
• Adaptable to changing priorities in a dynamic manufacturing environment