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Senior MES Engineer

  1. Ireland, West
Westport
  1. Contract
Competitive
  1. Life Sciences
37667
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Senior MES Engineer - Ireland, Westport - 12 Months Contract

Located on the picturesque west coast of Ireland, our Global pharmaceutical client is looking for a Senior MES Engineer to join their state-of-the-art pharmaceutical facility. They have invested $55 billion in research to discover and develop new medicines in the pursuit of scientific breakthroughs and changing people’s lives. They have 50,000 employees around the world and are continuing to grow.

Essential duties and responsibilities for this role include, but are not limited to, the following:
  • Design, create, write and/or make all required changes to MES Recipes, worksheets, equipment and material spec's including phase transition logic
  • Design, create, write and execute, test and validation protocols, risk assessments, and system documentation.
  • Design, create, write and/or make all required changes to ensure cleaning, equipment and product procedures are aligned to MES processes and vice versa.
  • Design, create, write and provide training for all other site personnel on their related MES roles and arrange system access.
  • Participate in MES knowledge exchanges, MES Governance meetings, and manage issues, work-around and fixes identified.
  • Provide support to other MES system users as required to ensure business continuity.
  • Participate in NPI projects from initiation to ensure MES system or hardware requirements are taken into consideration.
  • Keep other recipe authors up to date on MES changes
  • Documentation of all activities in line with cGMP requirements.
  • Cross training within the team and training of new team members.
  • Participation in continuous improvement programs to implement improvements in the quality, safety, environmental and production systems.
  • Adheres to and supports all EHS standards, procedures and policies.
Desirable Experience:
  • Third Level qualification in suitable manufacturing, engineering or business course and/or suitable experience.
  • Extensive authoring experience and has led or was technical lead on multiple implementation projects.
  • Be proficient with MES application and configuration rules and requirements including interfacing (preferably POMSnet).
  • Experience of batch processing operations in an FDA/HPRA regulated industry. Strong knowledge of cGMP and regulatory requirements relating to the pharmaceutical industry.
  • A good knowledge of IT systems is required for this role.
  • SAP knowledge/experience in MM, PP and IM modules.
  • Proven attention to detail and mental concentration, to always ensure total compliance with procedures.
If this role is of interest, please apply now!

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