We're looking for an experienced professional to join our team as a DeltaV Automation Specialist. As the primary technical point of contact for all DeltaV DCS-related projects and operations, you will be responsible for managing and coordinating technical activities to ensure compliant, reliable, and efficient automation of pharmaceutical API manufacturing processes.
Key Responsibilities:
* Liaise with cross-functional teams, including System Integrators, Site Process and Operation Teams, and Automation Engineers, to manage project progress and remove roadblocks or impediments.
* Coordinate with Scrum Master, Product Owner, and System Integrator to plan sprints.
* Manage Technical Queries Log and updates.
* Escalate issues to DeltaV Workstream Lead and PM as required.
* Lead the implementation, configuration, and validation of DeltaV systems in accordance with FDA regulations, 21 CFR Part 11, and GMP guidelines.
* Develop, configure, and test DeltaV control strategies, logic, and operator interfaces to meet pharmaceutical process requirements.
* Provide expert troubleshooting and root cause analysis for DeltaV system issues, ensuring minimal downtime and compliance with quality standards.
* Maintain detailed documentation, including system design specifications, validation protocols (IQ/OQ/PQ), change control records, and SOPs, to support audits and regulatory inspections.
* Train operators, engineers, and maintenance personnel on DeltaV system operation, change management, and compliance requirements.
* Collaborate with Emerson, system integrators, and quality assurance teams during audits, inspections, and vendor assessments.
* Identify and implement system enhancements to improve process control, data integrity, and operational efficiency while maintaining compliance.
Requirements:
* Bachelor's degree in Electrical Engineering, Instrumentation, Automation, or related technical field.
* Extensive experience with Emerson DeltaV DCS in a pharmaceutical or highly regulated manufacturing environment.
* Strong knowledge of pharmaceutical manufacturing processes and regulatory requirements (FDA, EMA, 21 CFR Part 11, GAMP 5).
* Experience with system validation lifecycle (IQ/OQ/PQ) and documentation practices.
* Proficiency with DeltaV software tools (Control Studio, AMS Suite, DeltaV Operate).
What We Offer:
A challenging role in a dynamic and innovative industry, with opportunities for growth and development.
A collaborative and supportive work environment.
The chance to work with a talented team of professionals who share your passion for automation and excellence.