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Senior Recruitment Consultant at PE Global
PE Global is recruiting for a Senior MES Engineer on behalf of our biopharmaceutical client in County Mayo. This is an initial 12-month contract, hybrid role.
Job Summary
* Maintain the MES environment; to author and maintain recipes and worksheets for the 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 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 5-year’s 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 083 094 0199 or alternatively send an up-to-date CV to paul.wheatley@peglobal.net
***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in Ireland***
Seniority level
* Seniority level
Not Applicable
Employment type
* Employment type
Contract
Job function
* Job function
Engineering, Information Technology, and Science
* Industries
Pharmaceutical Manufacturing, Biotechnology Research, and Medical Equipment Manufacturing
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