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MES Engineer
Employer undisclosedRole managed by a recruiter
Design, configure, and support MES systems and recipes for pharma manufacturing.
8d ago
Intermediate (4-7 years), Experienced (8-12 years), Expert & Leadership (13+ years)
Contractor
Westport, County Mayo, Ireland
Onsite
Role
What you would be doing
mes design
validation protocols
recipe management
mes governance
cgmp documentation
user support
- Design, create, write and execute, test and validation protocols, risk assessments, and system documentation.
- 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.
- Participate in MES knowledge exchanges, MES Governance meetings and manage issues, work-around and fixes identified.
- Participate in NPI projects from initiation to ensure MES system or hardware requirements are taken into consideration.
- Design, create, write and provide training for all other site personnel on their related MES roles and arrange system access.
- Design, create, write and/or make all required changes to MES Recipes, worksheets, equipment and material spec's including phase transition logic
- Keep other recipe authors up to date on MES changes
- Documentation of all activities in line with cGMP requirements.
- Provide support to other MES system users as required to ensure business continuity.
- Cross training within the team and training of new team members.
- Design, create, write and/or make all required changes to ensure cleaning, equipment and product procedures are aligned to MES processes and vice versa.
What you bring
mes
pomsnet
sap
degree
cgmp
attention
- Be familiar with MES application and configuration rules and requirements including interfacing (preferably POMSnet).
- SAP knowledge/experience in MM, PP and IM modules an advantage.
- Third Level qualification in suitable manufacturing, engineering or business course and/or suitable experience.
- Proven attention to detail and mental concentration, to ensure total compliance with procedures at all times.
- Experience of batch processing operations in an FDA/HPRA regulated industry. Strong knowledge of cGMP and regulatory requirements relating to the pharmaceutical industry.
- Requires extensive authoring experience preferably using POMSnet.
- A good knowledge of IT systems is required for this role.
Information not given or found
Training + DevelopmentInformation not given or found
Interview process
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Visa SponsorshipInformation not given or found
Security clearanceInformation not given or found
Your recruiter
Your recruiting firm
- Founded with the aim of providing top-tier staffing solutions for diverse sectors.
- Focus on long-term partnerships with clients, ensuring the right talent for specialized roles.
- Expert in recruiting for both large-scale projects and niche, high-demand sectors.
- Has become a trusted partner in sectors such as Industrial, Energy, and Infrastructure.
- Notable for a rapid response to market demands and changing industry trends.
- Experience in delivering recruitment services for large infrastructure and energy projects.
- Specializes in sourcing skilled professionals for both permanent and temporary roles.
- Recognized for working on complex and large-scale projects with a diverse client base.
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