Mes Engineer

Overview

MES Engineer - Ireland, Westport - 12 Months Contract.

Located on the west coast of Ireland, our global pharmaceutical client is seeking an MES Engineer to join their state-of-the-art facility.

The organisation has invested substantially in research and has around 50,000 employees worldwide and is continuing to grow.

Responsibilities

Design, create, write and / or make all required changes to MES Recipes, worksheets, equipment and material specs 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-arounds 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, preferably using POMSnet.

Familiar 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.

Seniorities

Entry level

Employment type

Contract

Job function

Engineering and Information Technology

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