Mes Engineer 1544

Specialists in Life Science Automation and IT Systems

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SimoTech provides manufacturing automation and IT systems engineering, project management and validation services.

We partner with life sciences companies to design, build, operate and optimise critical process automation systems that deliver fast track project delivery, operational efficiency, improve manufacturing agility and achieve regulatory compliance.

Why SimoTech

What is it like to work at SimoTech?

With a strong collaborative teamwork culture based on respect, trust and excellence, we play a critical partnering role to our clients' life-changing supply of products to patients.

In return, there is excellent salary, career progression, educational support and much more.

SimoTech has a new opportunity for an experienced

MES Engineer

to join our team supporting a global pharmaceutical organisation onsite in Limerick.

This is an exciting opportunity where you will gain exposure to next generation manufacturing, delivering improvements in safety and quality, as well as increased productivity and process performance.

This role will support the business processes and systems for a greenfield manufacturing site which will include advanced data collection and analysis platforms.

In particular, you will provide MES analyst support for an integrated set of systems that includes Syncade, DeltaV and SAP.

Key Responsibilities

Support site readiness activities to enable site start-up and ongoing operations.

Configures MES Syncade to support technical testing and installation with appropriate users and systems personnel.

Work with local and global IT groups to support delivery of manufacturing solutions.

Analyses business processes and needs to recommend or implement changes to systems and / or procedures.

Performs user requests for special support and / or extracts of data.

Works in all phases of systems development cycle (define, design and deliver solution) according to company and department guidelines.

Ensure compliance with Computer Systems Validation policies, standards, procedures and / or practices.

Assists Systems Operations, Desktops and / or telecommunications personnel on application of fixes and related troubleshooting.

Identify root cause and action plan to avoid the same situation occurs.

Qualifications

Bachelor's Degree in Information Technology, Computer Science, Engineering or related field.

At least 7 yearsrelevant Automation experience.

Pharmaceutical industry experience, supporting Emerson Syncade systems.

High proficiency in integrating Syncade with key manufacturing systems such as DeltaV and SAP.

Computer Systems Validation in cGMP regulated operations experience.

Knowledge of System Development Life Cycle.

Ideally 5 days on site but possibly 3 days minimum.

What SimoTech Can Offer

Role provides a high degree of autonomy to allow the successful candidate to reach their full potential.

Develop new skills and enhance technical ability by working with innovative technologies in a multi-disciplined environment.

Opportunity to work with large corporate clients on exciting capital projects.

By submitting my data (CV), I consent to SimoTech collecting and storing my personal data, as outlined in the SimoTech Privacy Statement which I have read.

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