MES Engineer - Ireland, Westport - 12 Month Contract
Located on the picturesque west coast of Ireland, our Global pharmaceutical client is looking for a MES Engineer to join their state-of-the-art 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 ****** employees around the world and are continuing to grow.
Essential duties and responsibilities for this role include:
Design, create, write and/or make all required changes to MES Recipes, worksheets, equipment and material specifications, including phase transition logic.
Design, create, write and execute, test and validate 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-around 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.
Document all activities in line with cGMP requirements.
Cross-train within the team and train new team members.
Participate in continuous improvement programs to implement improvements in the quality, safety, environmental and production systems.
Adhere to and support 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.
Familiarity 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.
Good knowledge of IT systems.
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.
If this role is of interest, please apply now!
Seniority level
Entry level
Employment type
Contract
Job function
Engineering and Information Technology
Location: Westport, County Mayo, Ireland
#J-*****-Ljbffr