AVEVA PI ENGINEER (301)

Réalta Technologies; Cork; On-site; EUR 50,000 - 70,000; Full time

Job summary

Réalta Technologies, a leader in automation and digital systems, seeks an experienced AVEVA PI Engineer in Cork. This role involves developing SDLC deliverables, ensuring technical alignment with project goals, and compliance with regulatory standards. Ideal candidates will possess a relevant degree and hands-on experience in pharma or biopharma settings.

Qualifications

• 3+ years’ experience in process control/information systems within pharma or biopharma.
• Hands-on experience with AVEVA PI and related tools is essential.
• Strong knowledge of GAMP and regulatory requirements.

Responsibilities

• Develop and review SDLC deliverables in line with company standards.
• Collaborate with teams on system architecture and specifications.
• Ensure technical delivery of Data Historian and Reporting systems.

Skills

Problem-solving

Project execution

Data interfaces

Networking fundamentals

Education

Bachelor’s degree in Engineering

Bachelor’s degree in Computer Science

Bachelor’s degree in Information Systems

Bachelor’s degree in Life Sciences

Tools

AVEVA PI

PI-AF

RT Reports

Kepware

FactoryTalk

Job description

Réalta Technologies is a leading automation and digital systems firm, delivering innovative solutions to the life sciences industry. We are seeking an experienced AVEVA PI Engineer to support us here in Cork.

Responsibilities

• Develop and review SDLC deliverables in line with company standards.
• Collaborate with Automation/IT teams on system architecture, specifications, and sequence of operations.
• Ensure technical delivery of Data Historian and Reporting systems aligned with project goals.
• Define and execute the project roadmap for Historian and Reporting systems.
• Communicate progress to project leadership and stakeholders.
• Support schedule, budget planning, and resource development.
• Guide contract firms and vendors during execution phases.
• Align project with the site's digitization strategy.
• Ensure compliance with company policies, cGMP, and regulatory requirements.
  
  

Requirements

• Bachelor’s degree in Engineering, Computer Science, Information Systems, or Life Sciences.
• 3+ years’ experience in process control/information systems within pharma or biopharma.
• Hands-on experience with AVEVA PI, PI-AF, RT Reports, Kepware, or FactoryTalk.
• Strong knowledge of data interfaces, networking, and infrastructure fundamentals.
• Familiarity with GAMP, ANSI/ISA S88/S95, and pharmaceutical industry regulations.
• Excellent problem-solving and project execution skills.