DeltaV Batch DCS Engineer — Pharma GMP Focus

Process Alliance LLC; Indianapolis (IN); On-site; USD 90,000 - 130,000; Full time

Job summary

Process Alliance LLC seeks a DeltaV Configuration Engineer to independently develop DeltaV Batch DCS configurations from FR/DS, translating narratives and P&IDs into control logic and HMI graphics for compliant manufacturing operations.

With 5+ years in pharmaceutical or regulated settings, you will ensure ISA-88 alignment, GMP compliance, and CSV documentation; certifications DeltaV 7009/7016 are required. Collaboration with process engineers and QA teams is essential.

Qualifications

• Bachelor's degree in Chemical, Electrical, or Controls Engineering or equivalent hands-on experience.
• 5+ years DeltaV Batch DCS configuration/coding experience in pharmaceutical or regulated manufacturing.
• Ability to independently develop DCS code from FR/DS with minimal oversight.
• Knowledge of ISA-88 batch standards, GMP, and CSV documentation practices.
• Strong attention to detail and documentation skills.
• DeltaV 7009 and 7016 certifications.

Responsibilities

• Independently develop DeltaV Batch DCS configuration, modules, phases, and recipes.
• Translate process narratives and P&IDs into control logic and HMI graphics.
• Ensure code complies with ISA-88, GMP, and site standards.
• Coordinate with process engineering to clarify requirements.
• Participate in design/code reviews and maintain version control.
• Support troubleshooting during testing, commissioning, and startup.
• Document configuration activities per CSV and QA requirements.
• Support FAT/SAT as SME for developed code.

Skills

DeltaV Batch DCS

FR/DS to code

ISA-88 standards

GMP/CSV docs

Attention to detail

DeltaV 7009/7016 certs

Education

B.S. in Chemical/Electrical/Controls

Job description

Process Alliance LLC seeks a DeltaV Configuration Engineer to independently develop DeltaV Batch DCS configurations from FR/DS, translating narratives and P&IDs into control logic and HMI graphics for compliant manufacturing operations.

With 5+ years in pharmaceutical or regulated settings, you will ensure ISA-88 alignment, GMP compliance, and CSV documentation; certifications DeltaV 7009/7016 are required. Collaboration with process engineers and QA teams is essential.