Senior Mes Engineer

Overview

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.

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 and has led or was technical lead on multiple implementation projects

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

Additional Information

Seniority level : Mid-Senior level

Employment type : Contract

Job function : Engineering and Information Technology

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