System Engineer - POMS MES

Read the overview of this opportunity to understand what skills, including and relevant soft skills and software package proficiencies, are required.

The Role :

• System Engineer - POMS MES
• Onsite role
• County Mayo
• Permanent or Contractor Opportunity

Role Brief :

The successful candidate will be responsible for the maintenance of the Manufacturing Execution System (MES) environment.

This is a POMSnet system and you will author and maintain recipes and worksheets for the manufacturing site using the POMSnet system.

You will also troubleshoot and provide solutions for both MES and SAP related problems in recipe execution and recipe authoring.

Core Tasks :

• Design, create, write and / or make all required changes to MES Recipes, worksheets, equipment and material specifications including phase transition logic.
• Design, create, write and execute test and validation protocols, risk assessments, and system documentation.
• Ensure cleaning, equipment and product procedures are aligned to MES processes and vice versa.
• Provide training for all other site personnel on their related MES roles and arrange system access.
• 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.
• Document all activities in line with cGMP requirements.
• Participate in continuous improvement programs to implement improvements in quality, safety, environmental and production systems.

Skills Brief :

• Third Level qualification in suitable manufacturing, engineering or business course and / or suitable experience.
• A minimum of 2 years authoring experience preferably using POMSnet.
• Familiarity 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 is an advantage.
• Proven attention to detail and mental concentration to ensure total compliance with procedures at all times.

Person Brief :

Candidates must have a B.Sc. Degree in Engineering or equivalent, with emphasis in software development, electrical, electronic or automation discipline, with a minimum of 3 years’ experience in industry, preferably in a pharmaceutical, biotechnology, blue chip or relevant GMP manufacturing environment.

The ideal candidate will have excellent communication and problem solving skills as well as strong stakeholder and vendor management skills.

As this role is fully onsite in County Mayo, the successful candidate must be based in County Mayo or within a reasonable commute.

Only candidates with a current valid work permit to work in Ireland can be considered due to project timelines.

Opportunity Brief :

This is an excellent opportunity to work with clients who are global leaders in their field, helping to develop and improve upon industry leading technology solutions.

SL Controls offers a supportive environment committed to employee development and wellness, along with a competitive and rounded compensation package, which rewards high performers.

Company Brief :

SL Controls are experts in the area of Equipment System Integration and System Support. We specialize in assisting our customers, including many of the world’s top multinational companies in the medical device and pharmaceutical sectors, achieve their Six Sigma and OEE targets.

Over the past 19 years, we have grown our business from a Sligo based enterprise into an international business with additional offices in Galway, Limerick, Leinster and Florida USA.

We pride ourselves on our expertise in industrial IT integration and regulatory compliance in support of global end users, OEMs and Technology providers.

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