IT/OT Automation Engineer for GMP/CSV (Pharma)

Progressive; Noord-Brabant; On-site; EUR 60,000 - 80,000; Full time

Job summary

A leading firm in pharmaceutical automation is seeking an IT/OT Automation Engineer to manage automation systems within a GMP-regulated environment. This full-time role involves ensuring compliance with regulatory standards and collaborating with cross-functional teams. A Bachelor’s degree in Engineering or Computer Science and over 5 years of experience in automation engineering are essential, as well as strong knowledge of automation systems. The position will be based in the Breda/Tilburg area.

Qualifications

• 5+ years of experience in automation engineering within GMP-regulated environments.
• Strong knowledge of automation systems and computer system validation.
• Experience in biotech manufacturing preferred.

Responsibilities

• Oversee OT systems for automated manufacturing lines.
• Manage the automation lifecycle: configuration, testing, and validation.
• Ensure compliance with FDA cGxP and corporate standards.

Skills

Automation systems

Computer system validation

GMP regulatory requirements

Excellent communication

Problem solving

Education

Bachelor's degree in Engineering or Computer Science

Tools

SCADA systems

Siemens TIA Portal

WinCC

Building Management System (BMS)

Environmental Monitoring System (EMS)

Job description

A leading firm in pharmaceutical automation is seeking an IT/OT Automation Engineer to manage automation systems within a GMP-regulated environment. This full-time role involves ensuring compliance with regulatory standards and collaborating with cross-functional teams. A Bachelor’s degree in Engineering or Computer Science and over 5 years of experience in automation engineering are essential, as well as strong knowledge of automation systems. The position will be based in the Breda/Tilburg area.