DeltaV Automation Coder (Configuration Engineer)This role sits within the Automation and Computer System Validation (CSV) division and is responsible for independently developing DeltaV Batch DCS configuration and code based on developing Functional Requirements (FR) and Design Specifications (DS). The engineer works closely with process engineering and process cell owners to translate process narratives and P&IDs into control logic, control modules, phases, recipes, and graphics that support reliable, compliant manufacturing operations.This role is well suited to a hands-on DeltaV Configuration Engineer who can take specifications and independently develop working, standards-compliant code with minimal oversight.Key ResponsibilitiesIndependently develop DeltaV Batch DCS configuration, control modules, phases, and recipes based on Functional Requirements and Design SpecificationsTranslate process engineering narratives and process P&IDs into control logic and HMI graphicsEnsure all code developed complies with ISA-88 batch standards, site automation standards, and GMP requirementsCoordinate with process engineering and process cell owners to clarify requirements and confirm alignment throughout developmentParticipate in internal design and code reviews to verify compliance with functional requirements, specifications, and standardsMaintain code version control, revision history, and change documentationSupport troubleshooting and debugging of DeltaV configuration during testing, commissioning, and startupDocument configuration development activities in accordance with CSV and quality requirementsSupport Factory Acceptance Testing (FAT) and Site Acceptance Testing (SAT) as the subject matter expert for developed codeQualifications:Bachelor's degree in Chemical, Electrical, or Controls Engineering, or equivalent hands-on experience5+ years of hands-on DeltaV Batch DCS configuration/coding experience in pharmaceutical or regulated manufacturingDemonstrated ability to independently develop DCS code from FR and DS with minimal oversightWorking knowledge of ISA-88 batch standards, GMP, and CSV documentation practicesStrong attention to detail and documentation skillsDeltaV 7009 and 7016 certificationsAdditional Preferences:Experience in pharmaceutical or other regulated manufacturing environmentsExperience supporting new/greenfield facility startupsExperience with electronic test management systems (e.g., Kneat, ALM)Notes:Location: Remote – Limited to no travel (<5%)