DeltaV Automation Engineer-Hybrid

Tipperary, Ireland | Posted on 08/29/2025

• Industry Pharma/Biotech/Clinical Research
• Work Experience 4-5 years
• Country Ireland

About PSC Biotech

Who are we?

PSC Biotech is a leading Biotech Consultancy firm foundedin 1996, headquartered in Pomona, California, USA, with Global operations inIreland, India, Singapore, Australia and the US, serving 350 clients in morethan 23 countries worldwide. We provide cloud-based software solutions forQuality Management and Regulatory Inspections, pharmaceuticals contractmanufacturing professionals, and metrology services to our clients.

'Take your Careerto a new Level'

PSC Biotech disrupts the conventional consultancy modelby aligning our EVP as one of the unique selling point which includes theopportunity to work with the most talented cohort of like-minded professionalsoperating in the Pharma/ Biotech Industry. We offer a permanent contract ofemployment giving exposure of working in Top Pharmaceutical client sites in adiverse-cultural work setting.

Employee ValueProposition

Employees are the "heartbeat" of PSC Biotech, we provideunparalleled empowering career development though Learning & Developmentin-house training mentorship through constant guidance to facilitate careerprogression. We believe in creating high performing teams that can exceed ourclient's expectations with regards to quality of all scalable and business unitdeliverables, staying under budget and ensuring timelines for our deliverablesare being met.

Overview:

• The Delta V Technical Coordinator is responsible formanaging and coordinating all technical activities related to the EmersonDeltaV Distributed Control System (DCS) Hardware and Software delivery toensure compliant, reliable, and efficient automation of pharmaceutical APImanufacturing processes.
  
• Familiarity with Agile Ways of working and support theimplementation of the DeltaV Software Delivery through Agile methodology.
  
• Liaising with multiple cross functional Agile teams ofSystem Integrators, Site Process and Operation Teams, Automation Engineers on aday-to-day basis to manage the progress of the sprint and to remove anyroadblocks or impediments that the team is facing.
  
• Coordinate with the Scrum Master, Product Owner andSystem Integrator on a day-today basis to plan every sprint.
  
• Manage Technical Queries Log and updates
  
• Manage escalations to DeltaV Workstream Lead and PM asrequired
  
• Coordination of Software delivery to meet site DSATdates.
  
• Responsible to maintain schedule adherence and tomitigate any delays.
  
• This role supports validation, regulatory compliance, andcontinuous improvement initiatives critical to Good Manufacturing Practices(GMP).
  
• API experience is preferable.
  
• Hybrid Role:3 dayson site (Tuesday, Wednesday and Thursday) mandatory required
  

Role Functions:

• SystemCoordination: Serve as the primary technical point of contact for allDeltaV DCS-related projects and operations within pharmaceutical manufacturingfacilities.
  
• Implementation& Validation: Lead the implementation, configuration, and validation ofDeltaV systems in accordance with FDA regulations, 21 CFR Part 11, and GMPguidelines.
  
• Configuration& Programming: Develop, configure, and test DeltaV control strategies,logic, and operator interfaces to meet pharmaceutical process requirements.
  
• Troubleshooting& Support: Provide expert troubleshooting and root cause analysis forDeltaV system issues, ensuring minimal downtime and compliance with qualitystandards.
  
• Documentation& Compliance: Maintain detailed documentation including system designspecifications, validation protocols (IQ/OQ/PQ), change control records, andSOPs to support audits and regulatory inspections.
  
• Training: Train operators, engineers, and maintenance personnel on DeltaV systemoperation, change management, and compliance requirements.
  
• Vendor & AuditCoordination: Collaborate with Emerson, system integrators, and qualityassurance teams during audits, inspections, and vendor assessments.
  
• Continuous Improvement: Identify and implement system enhancements to improve process control, dataintegrity, and operational efficiency while maintaining compliance.
  
• Risk Management: Participate in risk assessments and mitigation planning related to controlsystem changes and upgrades.
  
• Ensure Automation compliance with Global Policies,Procedures and Guidelines, regulatory requirements and execute current Goodmanufacturing Practices (cGMP) in the performance of day to day activities andall applicable job functions.
  

Knowledge, Skills,Education & Location Requirements:

• Bachelor's degree in Electrical Engineering,Instrumentation, Automation, or related technical field.
  
• Extensive experience with Emerson DeltaV DCS in apharmaceutical or highly regulated manufacturing environment.
  
• Strong knowledge of pharmaceutical manufacturingprocesses 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).
  
• Familiarity with industrial networking, cybersecurity,and protocols relevant to pharma automation.
  
• Excellent communication, documentation, and projectcoordination skills.
  
• Ability to work effectively with cross-functional teamsincluding Quality, Validation, Engineering, and Operations.
  
• Relevant certifications (e.g., DeltaV Certified Engineer,GAMP training) are highly desirable.