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Automation Commissioning Engineer

  1. Dublin
  1. Contract
Competitive
24354/AE
  1. Commisions, Qualification and Validation
Date Posted05 Feb 2020

This vacancy has now expired

As Dublin continues to embed itself as Irelands Pharmaceutical capital, we are seeking an Automation Commissioning Engineer to become part of a $500 million state of the art bio facility.

Located 15 minutes from Dublin Airport and just a short distance from the lively, vibrant, and cultural Irish capital, this leading biopharmaceutical organisation leads the way with state of the art technology on their one of a kind manufacturing facility. 

Position Summary

The MCS Automation Commissioning Engineer shall be responsible, as part of the client team, for the development and delivery of the Automation MCS System (Delta V) to enable the New Product, commissioning and qualification on their Bulk Drug Substance manufacturing facility in Dublin. The successful applicant will participate in the development and implementation of an MCS Solutions (Upstream & Downstream) in line with S88 standards for the BDS plant, and will manage the delivery of robust, compliant and cost effective MCS Solutions in line with agreed timelines for these key New Product capital project.

Principal Responsibilities
  • The Automation Commissioning Engineer will also co-ordinate the development of the Automation software and hardware to ensure alignment with various New Product Introduction schedules to enable equipment FAT’s, on-site SAT’s, commissioning and validation of the process systems to meet these projects schedules.
  • Works closely together with the other Automation Engineer to ensure deliverables are ready in time for the different milestones throughout the New Product Introduction projects.
  • Works closely together with the other Automation Engineer to ensure the defined standards are followed consistently in the project and the library modules are used as intended.
  • The Automation Commissioning Engineer will support the Commissioning Qualification and Validation (CQV) Teams in Shakedown and Verification of the DeltaV Software.
  • Design, code and test DeltaV software changes identified during Commissioning.
Qualifications
  • Min. of 5 years’ experience in the Biotech environment delivering Automation design / commission / start-up.
  • Min. of 5 years’ experience with DeltaV.
  • Has process understanding of production processes used like upstream, downstream processes or CIP, and/or has a deep knowledge of automation system architectures.
  • Ability to constructively challenge, defend and present technical aspects of system design.
 
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