DeltaV Technical Coordinator

Life Science Consultants

  • Tipperary
  • Permanent
  • Full-time
  • 7 days ago
LSC have a great contract opportunity for a DeltaV Technical Coordinator to join a top pharmaceutical company based in Tipperary. The site supports the complete pharmaceutical small molecule process for Phase III clinical to product release and market support. On site processes include API manufacture, formulation, OSD tableting, packaging and global logistics & distribution. The facility takes in raw chemicals and ships finished medicines to end users. This site has grown from an API site to a strategically important campus that supports critical stages of the company's drug lifecycle.If you have a 5+ years of working in an DeltaV/CSV role in a regulated environment are ready for your next challenge, this could be the perfect project for you!ABOUT THE PROJECT - KEY RESPONSIBILITIES:
  • The Delta V Technical Coordinator is responsible for managing and coordinating all technical activities related to the Emerson DeltaV Distributed Control System (DCS) Hardware and Software delivery to ensure compliant, reliable, and efficient automation of pharmaceutical API manufacturing processes.
  • Familiarity with Agile Ways of working and support the implementation of the DeltaV Software Delivery through Agile methodology.
  • Liaising with multiple cross functional Agile teams of System Integrators, Site Process and Operation Teams, Automation Engineers on a day-to-day basis to manage the progress of the sprint and to remove any roadblocks or impediments that the team is facing.
  • Coordinate with the Scrum Master, Product Owner and System Integrator on a day-today basis to plan every sprint.
  • Manage Technical Queries Log and updates
  • Manage escalations to DeltaV Workstream Lead and PM as required
  • Coordination of Software delivery to meet site DSAT dates.
  • Responsible to maintain schedule adherence and to mitigate any delays.
  • This role supports validation, regulatory compliance, and continuous improvement initiatives critical to Good Manufacturing Practices (GMP).
  • API experience is preferable.
ABOUT YOU - ARE YOUR SKILLS A MATCH?
  • 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).
  • Familiarity with industrial networking, cybersecurity, and protocols relevant to pharma automation.
  • Excellent communication, documentation, and project coordination skills.
  • Ability to work effectively with cross-functional teams including Quality, Validation, Engineering, and Operations.
  • Relevant certifications (e.g., DeltaV Certified Engineer, GAMP training) are highly desirable..
Please note that for our contracting opportunities in the pharmaceutical sector in Ireland, candidates must possess either a Stamp 1G or a Stamp 4 visa. We regret that we are unable to provide visa sponsorship at this time. Thank you for your understanding.Apply via this advert or contact Paul O'Driscoll on 021 4777 329 if you have any more questions about this opportunity!

Life Science Consultants