Our client, a global healthcare company is currently recruiting for an MES Engineer to join their growing team in Westport, Co. Mayo.

Responsibilities (full job description available on request):

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.
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.
Participate in NPI projects from initiation to ensure MES system or hardware requirements are taken into consideration.
Documentation of all activities in line with cGMP requirements.

Requirements:

Third Level qualification in manufacturing, engineering or business discipline.
A minimum of 2 years 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.
SAP knowledge/experience in MM, PP, and IM modules an advantage.

For a confidential discussion on the role and the organisation please contact Emma Barry today.

091 706719

MES Engineer