Explore a rewarding opportunity as a Deltav Automation Specialist in the pharmaceutical industry.
About the Role
The Deltav Automation Specialist is responsible for overseeing technical projects related to Emerson Delta V Distributed Control System (DCS) Hardware and Software delivery. This includes ensuring compliant, reliable, and efficient automation of pharmaceutical API manufacturing processes.
* Collaborate with Agile teams, including System Integrators, Process Teams, and Automation Engineers to manage project progress and remove obstacles.
* Coordinate with Scrum Masters, Product Owners, and System Integrators to plan every project.
* Manage Technical Queries Log and updates, and escalate issues to the Delta V Workstream Lead and Project Manager as needed.
Serve as the primary technical point of contact for all Delta V DCS-related projects and operations within pharmaceutical manufacturing facilities.
Main Responsibilities
Lead the implementation, configuration, and validation of Delta V systems according to FDA regulations, 21 CFR Part 11, and GMP guidelines.
* Develop, configure, and test Delta V control strategies, logic, and operator interfaces to meet pharmaceutical process requirements.
* Provide expert troubleshooting and root cause analysis for Delta V system issues, ensuring minimal downtime and compliance with quality standards.
Maintain detailed documentation, including system design specifications, validation protocols, change control records, and SOPs to support audits and regulatory inspections.
Train operators, engineers, and maintenance personnel on Delta V system operation, change management, and compliance requirements.
Collaborate with Emerson, system integrators, and quality assurance teams during audits, inspections, and vendor assessments.
Requirements
Bachelor's degree in Electrical Engineering, Instrumentation, Automation, or a related technical field.
* Extensive experience with Emerson Delta V DCS in a pharmaceutical or highly regulated manufacturing environment.
* Strong knowledge of pharmaceutical manufacturing processes and regulatory requirements.
* Experience with system validation lifecycle and documentation practices.
* Proficiency with Delta V software tools.