Automation Engineer (Rockwell/Siemens, SCADA) Must have a valid EU Work Permit

PACIV, a global leader in industrial automation solutions with offices in Ireland, United States and Puerto Rico, and servicing the Life Sciences, F&B and Utilities industries, is looking for regular employment-based Automation Engineer(s) for its Ireland office.

Job Description:

• Define, develop and deploy automation.
• Take leadership during the entire life cycle of automation projects, from concept to feasibility and from design and test to production.
• Develop automation User requirements and specifications.
• Solicit quotations from automation suppliers. Evaluate supplier quotations to determine the best combination of technical solution, cost and timing.
• Develop budget and schedule for projects and manage projects to stay within them.
• Conduct equipment design reviews and provide design guidance to suppliers.
• PLEASE NO AGENCIES AT THIS TIME
• Manage automation suppliers through all phases of projects.
• Provide on-site support during machine build, debug and testing/qualification.
• Supervise installation and testing to verify requirements and specifications are met.
• Draft qualification protocols and support equipment qualification activities.
• Ensure compliance procedures, cGMP,
• Ensure that all Health, Safety and Environmental requirements are fulfilled.
• Open to travel to support development, FAT and other activities.

KEY COMPETENCIES REQUIRED:

• Flexible with High Attention to Detail with super quality                 
• Pro-active approach to Work         
• Excellent Communication Skills     
• Analytical Skills                 
• Team Player
• Highly Computer Literate
• Planner & Organiser                     
• Active Listener
• Continuous Improvement Focused

QUALIFICATIONS & EXPERIENCE

ESSENTIAL:

• Third Level Qualification in Automation, IT Systems, Electronic/Mechatronic Engineering.
• Experience with Rockwell ,Siemens,SCADAplatforms and other PLC  systems
• Ability to interpret engineering drawings/specifications.
• Experience of working within a regulated lifescience manufacturing environment.
• Must have a valid EU Work Permit