Delta V Batch Engineer Onsite

Delta V Batch Engineer - Life SciencesWork Model: OnsiteJob Type: Full-timeIndustry: Pharmaceutical / Biotech / Life SciencesJob SummaryA DeltaV Lead Engineer in the life science industry is responsible for managing the implementation and maintenance of Emerson's DeltaV automation system within pharmaceutical, biopharmaceutical, or biotechnology manufacturing environments. This role oversees DeltaV-related projects, ensures compliance with industry regulations, and provides deep technical expertise and support. The engineer will drive system performance, troubleshooting, documentation, and continuous improvement across the DeltaV ecosystem.Key ResponsibilitiesDesign, implement, maintain, and support Emerson DeltaV systems in a GMP-regulated manufacturing environment.Troubleshoot and resolve technical issues related to DeltaV hardware, software, and batch control strategies.Ensure compliance with cGMP, GAMP 5, 21 CFR Part 11, and other regulatory standards through proper validation and documentation.Lead and manage DeltaV-related automation projects, including planning, scheduling, and resource coordination.Collaborate with cross-functional teams including Operations, IT, Engineering, and Quality to integrate DeltaV with broader manufacturing processes.Provide ongoing maintenance, periodic reviews, and upgrades to ensure system integrity and performance.Develop and maintain technical documentation including design specifications, user manuals, SOPs, and change control records.Identify and implement continuous improvement opportunities within the DeltaV system and related automation environments.Train operators, engineers, and maintenance personnel on DeltaV system functionality, troubleshooting, and operational best practices.Support and collaborate on related technologies (PLC, SCADA, OSI PI, etc.) as needed.Required QualificationsProven hands-on experience with Emerson DeltaV system design, configuration, implementation, and support.Experience in pharmaceutical, biopharmaceutical, or biotechnology manufacturing environments.Strong understanding of automation principles including DCS, PLCs, and SCADA systems.Expertise in regulatory and validation frameworks (cGMP, GAMP 5, 21 CFR Part 11).Excellent analytical and problem‐solving skills with the ability to troubleshoot complex automation issues.Strong communication, collaboration, and documentation skills.Project management experience overseeing automation initiatives from concept to delivery.Please note this role is not able to offer visa transfer or sponsorship now or in the future*CompensationThe annual salary range for this position is in the range of $90,000 to $109,000, depending on experience, skills, and geographic location. This role may also be eligible for performance‐based bonuses in accordance with company compensation policies.Travel - Readiness to travel as and when needed for project discussion, planning workshops with client, FAT and for Business Cut OversBenefitsComprehensive medical, dental, and vision coverage401(k) retirement savings plan with company matchPaid time off (PTO), paid holidays, and wellness daysLife insurance and disability coverageEmployee Assistance Program (EAP) and mental health supportProfessional development, training, and certification reimbursement