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Maximo/ CMMS Engineer

  1. France
Dublin
  1. Contract
Competitive
  1. Life Sciences
36049
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Maximo/CMMS Engineer - Pharmaceuticals - Ireland, Dublin - 12-Month Contract 

Are you looking for your next contract, and fancy the opportunity to work in Dublin? Our client, a global biotechnology organisation, are recruiting for a Maximo Engineer to join their team in the construction of their new biopharmaceutical production plant. This new build facility will be vital vehicle in helping our client continue global access to life changing therapeutics.


Responsibilities include:
  • CMMS (computerised maintenance management system) engineer
  • This person will be responsible for CMMS - Maximo. Organise calibration, engineering, assisting the building, populating and managing the Master Project Database (MPD) which will be central to all CQV execution efforts and download of information into the CMMS System (Maximo).
  • Liaise with A&E firm to ensure timely handover of all Engineering Deliverables (Line List, Valve List, Instrument Index, and Equipment List).
  • Liaise with Vendors in relation to spare parts listing for all Equipment.
  • Assist with the review all Vendor spares information, prior to download into MPD.
  • Liaise with Construction Group to ensure all Receipt Verification (RV) requirements are met
  • Assist the CQV Lead MPD Engineer to create and coordinate all Receipt Verification (RV) and Installation Qualification (IQ) Check sheets
  • Liaise with Construction, CQV and CMMS Units in relation to RV/IQ required deliverables.
Experience Required: 
  • Report, standards, policy writing skills required
  • SAP knowledge and experience preferred
  • Proficiency in Microsoft Office and job-related computer applications required
  • Lean Six Sigma Methodology experience desired
  • Bachelor’s Degree or higher preferred; ideally in a related Engineering discipline
  • Experience and/or a particular skill set in their area of expertise that adds value to the business; ideally in a manufacturing, preferably GMP setting


If this role is of interest, please apply now!
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