About the Role

Lead the design, implementation, and project management of large-scale automation projects within the biopharmaceutical and medical device manufacturing space. You’ll deliver cGMP-compliant Emerson DeltaV solutions from concept to commissioning, collaborating with multidisciplinary teams to ensure regulatory compliance, efficiency, and innovation

Key Responsibilities

Design and implement DeltaV control systems for complex capital projects
Develop batch sequencing, phase logic, and recipe structures per ISA-88 standards
Create high-performance HMIs in DeltaV Live and DeltaV Operate following ISA-101 guidelines
Configure and integrate industrial networks (Ethernet/IP, Modbus TCP/IP, Profibus, Foundation Fieldbus, OPC UA)
Manage schedules, budgets, and resources for on-time, within-budget project execution
Ensure adherence to cGMP, GAMP5, and 21 CFR Part 11 compliance requirements
Mentor and guide junior engineers and cross-disciplinary teams
Oversee FAT, SAT, and acceptance testing activities

Required Qualifications

8–15 years hands-on Emerson DeltaV system engineering experience
Proficiency in DeltaV Live and DeltaV Operate
Strong knowledge of ISA-88 batch processing and ISA-101 HMI principles
Experience in regulated Life Sciences environments (cGMP, GAMP5)
Expertise with industrial communication protocols: Ethernet/IP, Modbus TCP/IP, Profibus, Foundation Fieldbus, OPC UA
Proven leadership in managing large capital automation projects

Preferred Qualifications

Experience with Rockwell Automation, Siemens PCS7, or Ignition SCADA
Electrical design skills (MCCs, VFDs, control panels)
Historian integration and advanced control strategies

Work Environment

Office-based with commissioning site visits (~25% travel)
Frequent use of engineering tools, control systems, and networking equipment
Occasional lifting and physical work during commissioning activities