Job Description
PE Global is currently recruiting for a MES Engineer on behalf of our pharmaceutical client based in Mayo. This is a long-term 23-month contract. Purpose Maintain the MES (POMSnet) environment; to author and maintain recipes and worksheets for the Westport site. Provide technical guidance and solutioning to other MES Engineers. Act as site escalation point for complex or challenging troubleshooting or recipe design. Provide project management guidance and expertise to the MES function. Responsibilities 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. 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. Liaise with Global MES on Westport required system improvements. 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. Requirements Third Level qualification in suitable manufacturing, engineering or business course and/or suitable experience. A minimum of 2-5 years authoring experience and has led or was technical lead on multiple implementation projects. Be 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. Interested candidates should submit an updated CV. Please click the link below to apply, call Paul Wheatley on or alternatively send an up-to-date CV to ***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in Ireland*** Although it is not possible for us to respond to all applications, we at PE Global will do our upmost to give you feedback on your application. You have sent your Cv into us as a company and even though you have sent your CV to a particular position, we are making the reasonable assumption that you are active on the job market and as part of our normal recruitment service we will discuss other suitable positions with you. You are free to opt out of this so please specify in your application to us if you just want to be contacted in relation to a specific vacancy. Your Cv is sent to a central recruitment inbox which a number of people in the applicable PE Global division have access to and so this means that you might not be contacted by the named person in this advert. Skills: POMSnet MES Syncade Werum PAS-X