DeltaV Engineer

Industry: Pharmaceutical / Life Sciences Manufacturing

Role Overview

We are seeking a hands-on DeltaV Engineer with CSV exposure to support GMP-regulated pharmaceutical manufacturing projects. The ideal candidate must have deep technical experience at the lower module level (CM/EM/Phase logic) along with involvement in validation lifecycle activities.

• 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.

• 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.