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 role will provide client side design input at the Basis of Design, Detailed Design, Commissioning, Qualification and handover stages of a design project for a Pharmaceutical facility. Particular relevance would be previous experience in Large Scale Capital Projects, in Biologics, Pharma or fill/finish Facilities. The scope of the role, may also require design input and support during the project phases for various ancillary areas such as the Fill/Finish Facility, the existing Warehouse, general site infrastructure, which are all collectively managed as part of the project.

Duties:

• To support client side design team in its efforts associated with the design of the new facility and ancillary projects (Laboratory reconfiguration, Canteen expansion and Warehouse Modifications) as directed by the Design Manager.
• To coordinate client side design activities by liaising with Design Team Resources, Site SME’s and Client’s Engineering Technical Authority (ETA) in delivering the Canteen and Laboratory designs.
• To partake in client side design reviews and to coordinate the participation of all stakeholders.
• To coordinate and participate in cross functional package, area, or overall design team reviews as required in support of client’s overall design goals and expectations
• To support site facility and utility walkdowns by the third Party designers and to schedule such activities with site Facilities Group, Engineering and the Laboratory End-User.
• To act as a point of contact for all technical queries in relation to assigned scopes of work
• To manage / monitor project action logs / RFI’s / review cycles
• To be available to execute scopes of work (Manage / Coordinate) in support of the overall project schedule. (Knowledge of CE Marking / Legislation would be an advantage)
• To coordinate with Site Facilities, Engineering and End Users in relation to the Site Engineering Change Management process.
• To liaise with C&Q, in support of the commissioning / qualification of the Laboratory and Canteen systems.
• To support the handover process of the systems / facilities to Engineering and Laboratory End-Users.

• Minimum of 5 years of experience in pharmaceutical Facility, with experience of Engineering Documentation Management, Project Execution and/or Facility Design.
• Degree level qualification in Mechanical, Electrical Engineering, CSA background, or similar/equivalent.
• Ability to challenge, defend and present technical aspects of design and commissioning.
• An understanding of interdisciplinary interfaces and an ability to resolve conflicting priorities.