We are currently recruiting for an experienced MES Engineer to support our clients pharmaceutical manufacturing site.
This contract role plays a critical part in a digitilasation project for our client.
Purpose Maintain the MES (POMSnet) environment, including authoring and maintaining recipes and worksheets.
Troubleshoot and provide solutions for MES and SAP issues related to recipe execution and authoring.
Key Responsibilities Design, create, write, and maintain MES recipes, worksheets, equipment, and material specifications, including phase transition logic.
Design, execute, test, and document validation activities, including protocols, risk assessments, and system documentation.
Ensure alignment between cleaning, equipment, and product procedures and MES processes.
Develop and deliver MES-related training for site personnel and coordinate system access.
Provide ongoing support to MES users to ensure business continuity.
Participate in MES governance forums and knowledge-sharing activities; manage issues, workarounds, and system fixes.
Liaise with global MES teams to support system enhancements and improvements.
Support New Product Introduction (NPI) projects to ensure MES system and hardware requirements are addressed from project initiation.
Communicate MES updates and changes to other recipe authors.
Maintain accurate documentation in compliance with c GMP requirements.
Cross-train within the team and support onboarding and training of new team members.
Contribute to continuous improvement initiatives across quality, safety, environmental, and production systems.
Adhere to and actively support all EHS standards, procedures, and policies.
Requirements Third-level qualification in manufacturing, engineering, business, or a related discipline, and/or equivalent relevant experience.
Minimum of 2 years' MES recipe authoring experience, preferably using POMSnet.
Strong understanding of MES application configuration rules and system interfacing (preferably POMSnet).
Experience with batch processing operations in an FDA/HPRA regulated environment.
Strong knowledge of c GMP and pharmaceutical regulatory requirements.
Solid IT systems knowledge.
SAP experience or knowledge (MM, PP, IM modules) is an advantage.
Proven attention to detail and ability to maintain high levels of accuracy and compliance.
For a confidential conversation about the role please apply for the role or contact Owen Clancy at oclancy@sterlingengineeringeu.com By applying to this job post you agree that Sterling Engineering may process your personal data for recruitment purpose.
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