
Delta V Technical Coordinator
- Co Tipperary
- Contract
- Full-time
- Support software delivery using Agile methodology.
- Collaborate with cross-functional teams (system integrators, operations, automation) to track sprint progress and resolve blockers.
- Plan sprints with Scrum Master, Product Owner, and integrators.
- Manage technical query log and escalations.
- Ensure software delivery meets DSAT milestones and schedule adherence.
- Support validation, regulatory compliance, and continuous improvement (GMP).
- System Coordination: Primary technical contact for Delta V DCS projects and operations in pharmaceutical manufacturing.
- Implementation & Validation: Lead Delta V implementation, configuration, and validation per FDA, 21 CFR Part 11, and GMP.
- Configuration & Programming: Develop and test control strategies, logic, and operator interfaces.
- Documentation & Compliance: Maintain design specs, validation protocols (IQ/OQ/PQ), change controls, and SOPs for audits.
- Troubleshooting & Support: Provide expert support and root cause analysis to minimize downtime and ensure compliance.
- Training: Providing training on system operation, compliance, and change management.
- Vendor & Audit Coordination: Partner with Emerson, integrators, and QA during audits and inspections.
- Continuous Improvement: Drive enhancements to improve control, data integrity, and efficiency.
- Risk Management: Support risk assessments and mitigation for system changes and upgrades.
- A Bachelor’s degree in Automation, Electrical Engineering, Instrumentation, or related technical field.
- API experience is preferable.
- Vast experience with Emerson Delta V DCS in a Pharmaceutical or highly regulated manufacturing environment.
- Proficiency with Delta V software tools (Control Studio, Delta V Operate, AMS Suite).
- Knowledge of industrial networking, cybersecurity, and protocols relevant to Pharma automation.
- Extensive knowledge of pharmaceutical manufacturing processes and regulatory requirements such as FDA, EMA, 21 CFR Part 11, GAMP 5.
- Proven track experience with documentation practices and system validation lifecycle (IQ/OQ/PQ).
- Strong communication, documentation, and project coordination skills.
- Relevant certifications (e.g., Delta V Certified Engineer, GAMP training) is an advantage.