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).
- 46 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.
Job Title: DeltaV Engineer (Automation & CSV) Industry: Pharmaceutical / Life Sciences Manufacturing Role OverviewWe 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...
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).
- 46 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.
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