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.
About the client
About the client
Information not given or found
Role
Description
mes recipes
validation protocols
user support
process improvement
npi integration
cgmp documentation
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.
Participation in continuous improvement programs to implement improvements in the quality, safety, environmental and production systems.
Cross training within the team and training of new team members.
Keep other recipe authors up to date on MES changes
Design, create, write and/or make all required changes to MES Recipes, worksheets, equipment and material spec's including phase transition logic
Documentation of all activities in line with cGMP requirements.
Design, create, write and provide training for all other site personnel on their related MES roles and arrange system access.
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 support to other MES system users as required to ensure business continuity.
Requirements
detail
it systems
technical lead
mes
cgmp
sap
Proven attention to detail and mental concentration, to always ensure total compliance with procedures.
A good knowledge of IT systems is required for this role.
Extensive 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.
Third Level qualification in suitable manufacturing, engineering or business course and/or suitable experience.
SAP knowledge/experience in MM, PP and IM modules.