DeltaV Engineer (Automation & CSV)

Job Title: DeltaV Engineer (Automation & CSV) 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. Key Responsibilities 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. Qualifications & Experience 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.