We’re currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Dublin. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do.

This person will have previous relevant experience of Pretreatment Systems, Clean Steam, WFI and Process Air generation and distribution systems, to provide client side design input at Detailed Design, Commissioning, Qualification and handover stages of a design project for a Fill/Finish Building.

The scope of the role also includes design input and support during the project phases for various ancillary areas such as the existing Warehouse, a new -30Deg Coldroom, Laboratory reconfigurations and general site infrastructure, which are all collectively managed as part of the expansion project.

Due to the nature of the role, the Clean Utilities Engineer will also be required to support FAT’s at vendor sites at times during the project.

Duties:

• To support company’s client side design team in its efforts associated with the new expansion.
• To provide technical expertise working with other project stakeholders, in order to achieve design deliverables
• To track, manage and communicate adherence to discipline project milestones
• To coordinate client side clean utilities (Clean Steam / WFI / CA) design by liaising with Site SME’s and company’s Engineering Technical Authority (ETA)
• To assist client side design reviews in the area of Clean Utilities for the expansion project.
• To participate in cross functional package, area, or overall design teams as required in support of company’s overall design goals and expectations.
• To input into Technical Assessment in support of the instrumentation framework, and/or procurement agreements.
• To participate in design reviews, model reviews, etc., and to input on technical elements of the design
• To execute Drawing, URS, HDS, SDS, Equipment & Instrument Specifications and other reviews associated with the company Clean Utility installations.
• To participate in CMSAT’s / Loop checking, including any trouble shooting activities
• To provide input and assistance to Automation, C&Q and Validation in terms of equipment packages as required.
• To participate in the design reviews and specifications review of any Vendor Package Equipment in the new Facility.
• Provide attendance / assistance for FAT’s / SAT / C&Q and Validation activities at various locations, site or Vendor, as required.
• To provide input into the calibration program for clean utilities. To coordinate with company’s site Metrology Group to ascertain calibration requirements and to ensure the execution of calibrations, both equipment and field instruments, in line with these requirements.
• To liaise with the site Maintenance Group and to ensure that any data gathering required to support the MAXIMO system requirements.

• Minimum of 5 years of experience in pharmaceutical design / build / commission / start-up with direct responsibility for Engineering Documentation, Project Execution or Facility Design.
• Degree level qualification in Chemical / Mechanical Engineering, or similar/equivalent.
• Direct experience in a similar scale project.
• Ability to challenge, defend and present technical aspects of design and commissioning.