Your new company

Your new role

• Develop and modify Control Modules (CM), Equipment Modules (EM), and Phase-level logic, including CMI/EMI modules.
• Perform module coding, parameter configuration, and support batch architecture aligned with S88 standards.
• Support system integration, testing (FAT/SAT), commissioning, and startup activities.
• Participate in and execute CSV lifecycle activities including URS, FDS, DDS review, IQ/OQ protocol execution, and PQ support.
• Ensure compliance with GAMP5, 21 CFR Part 11, and data integrity requirements.
• Provide troubleshooting support for module logic, batch execution issues, and system performance optimization.
• Collaborate with cross-functional teams including Manufacturing, QA, CQV, and IT.

What you'll need to succeed

• Bachelors degree in Engineering (Electrical, Instrumentation, Chemical, or related discipline).
• 4–6+ years of experience in DeltaV automation within pharmaceutical/biotech environments.
• Strong hands-on exposure to CM/EM configuration, phase logic development, and system architecture.
• Practical experience in coding, parameter handling, and module-level troubleshooting.
• Experience working in GMP-regulated environments with validation documentation and compliance.
• Good understanding of batch processes and ISA-88 concepts.

What you'll get in return

You will be given the chance to continuously grow in the company due to the expanding business entity, whilst being a part of the team in the growing business.

What you need to do now