6 Mes Engineer 1544 jobs in Ireland

Location - Westport, Mayo GerTEK is an engineering consultancy company specialising in project management, talent solutions and commissioning qualification and validation services. We partner with many of the world's largest life science & technology companies who entrust in us to deliver their most strategic and important projects. Role title - MES Engineer (Senior) - Westport Overview: Maintain the MES (POMSnet) environment; to author and maintain recipes and worksheets for the Westport 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 the Global MES on Westport requiring 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. Requirements: Third Level qualification in suitable manufacturing, engineering or business course and/or suitable experience. A minimum of 7 years authoring experience and has led or was technical lead on multiple implementation projects. 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. SAP knowledge/experience in MM, PP and IM modules. To start the process click the Continue to Application or Login/Register to apply button below.

**23 month FTC role in Carrigtwohill, Cork**
**Who we want:**
Senior MES Engineer on the Digital Solutions team to be responsible for setting up best in class manufacturing processes to enable the different value streams in the Patient Specific End to End project.
**What you will do:**
You will innovate and develop the various project elements with an emphasis on the manufacturing process, technology and procedures required for the
manufacture of new products adhering to procedures set out by Quality and
Regulatory Affairs.
- Independently research, design, develop, modify, and verify medical device systems
- Translate user needs to system requirements
- Modify existing system architectures or test designs
- Create new system architectures or test designs for simple product or features
- Allocate and decompose requirements on a multi-disciplinary (electrical, mechanical, software) project using modeling, simulation, budgeting, or mathematical techniques
- Lead Concept Phase activities for a feature
- Analyze and correct complex product design issues using independent judgment
- Lead analytical studies, including trade studies, sensitivity studies, optimization studies, performance assessments, and design assessments
- Lead system integration testing and verification activities
- Contribute to Product Risk Management activities
Business Responsibilities:
- Advance solutions by applying in-depth knowledge of customer needs, market, and competitive offerings
- Apply detailed knowledge of clinical procedures to author design inputs
- Support Voice of Customer sessions internally and with clinicians
- Demonstrate developing financial acumen
Med Device Compliance:
- Be proficient with and mentor others in usage of industry standards, including design requirements and test strategies per applicable regulations
- Lead creation and refinement of engineering documentation, such as the Design History file
- Follow and mentor others on R&D procedures like design controls and risk management, per the Quality Management System
General Responsibilities:
- Work cooperatively with all stakeholders to ensure project success
- Identify and support the creation of or improvements to procedures, policies, processes, systems, and technology
- Support and execute segments of complex multifunctional teams to advance projects through the design /development/launch process
- Deliver high quality results with passion, energy, and drive to meet business priorities
- Collaborate with cross-functional teams to build partnership to achieve business objectives
**Minimum Qualifications:**
- Bachelor's degree in Software Engineering/ Computer Science or related discipline & 4+ years of work experience
**Preferred Qualifications:**
Technical Skills:
- Knowledgeable programming skills. Design new components applying various concepts design concepts and patterns
Design and Development Skills:
- Knowledgeable with integrated development environments (IDE) for projects
- Knowledgeable with tools for static/dynamic analysis, memory management, code coverage and techniques for analyzing software
- Knowledge in integration and deployment processes
Software Process Skills:
- Software Development Life Cycle processes
- Knowledge in creating estimates for code implementation time/resource for assigned tasks and projects
- Knowledge from using Application Lifecycle Management /Traceability tools.
- Knowledge of regulatory and compliance standards applied to the SDLC (Software Development Life Cycle)
This role will be posted for a minimum of 3 days.
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.

Job Title: Senior MES Engineer (Emerson Syncade) Location: Ireland (Hybrid, with client site presence) Type: Permanent | Full-Time About the Company We are a newly established Ireland-based technical services team, backed by a US systems integrator with over 90 years experience in automation and digital solutions. Our mission is to deliver world-class MES and automation expertise to the life sciences sector, helping manufacturers achieve the highest standards of quality, safety, and efficiency. The Role We are seeking a Senior MES Engineer (Emerson Syncade) to deliver, support, and enhance MES solutions for leading life sciences manufacturers. This is a customer-facing role where youll work across full project lifecycles and play a key part in shaping our growing Irish team. Key Responsibilities Deliver Syncade projects: installation, configuration, testing, validation, and go-live support Act as a trusted technical partner to life sciences clients Troubleshoot issues and optimise MES performance Support compliance with GAMP5, FDA 21 CFR Part 11, and data integrity standards Collaborate with cross-functional teams and provide technical guidance Mentor junior engineers as the team grows What Were Looking For 58+ years MES experience (Emerson Syncade strongly preferred) Hands-on expertise in key Syncade modules: EBR, Materials, Weigh & Dispense, Equipment Tracking Strong knowledge of SQL, VBScript, XML/XSL and system integrations Understanding of MESDeltaV interfaces and other manufacturing systems Experience with system validation (IQ/OQ/PQ) and regulatory compliance Excellent communication and client-facing skills Degree in Engineering or Computer Science Why Join Be part of building a new Ireland team from the ground up Work directly with leading life sciences manufacturers Progress towards senior technical or leadership roles Hybrid working model with client engagement Dynamic environment backed by the stability of a trusted US parent company How to Apply If you have strong Syncade MES experience and want to be part of shaping a new team in Ireland, wed love to hear from you. Apply today with your CV. #LI-DB4

Job Title: Senior MES Engineer (Emerson Syncade) Location: Ireland (Hybrid, with client site presence) Type: Permanent | Full-Time About the Company We are a newly established Ireland-based technical services team, backed by a US systems integrator with over 90 years experience in automation and digital solutions. Our mission is to deliver world-class MES and automation expertise to the life sciences sector, helping manufacturers achieve the highest standards of quality, safety, and efficiency. The Role We are seeking a Senior MES Engineer (Emerson Syncade) to deliver, support, and enhance MES solutions for leading life sciences manufacturers. This is a customer-facing role where youll work across full project lifecycles and play a key part in shaping our growing Irish team. Key Responsibilities Deliver Syncade projects: installation, configuration, testing, validation, and go-live support Act as a trusted technical partner to life sciences clients Troubleshoot issues and optimise MES performance Support compliance with GAMP5, FDA 21 CFR Part 11, and data integrity standards Collaborate with cross-functional teams and provide technical guidance Mentor junior engineers as the team grows What Were Looking For 58+ years MES experience (Emerson Syncade strongly preferred) Hands-on expertise in key Syncade modules: EBR, Materials, Weigh & Dispense, Equipment Tracking Strong knowledge of SQL, VBScript, XML/XSL and system integrations Understanding of MESDeltaV interfaces and other manufacturing systems Experience with system validation (IQ/OQ/PQ) and regulatory compliance Excellent communication and client-facing skills Degree in Engineering or Computer Science Why Join Be part of building a new Ireland team from the ground up Work directly with leading life sciences manufacturers Progress towards senior technical or leadership roles Hybrid working model with client engagement Dynamic environment backed by the stability of a trusted US parent company How to Apply If you have strong Syncade MES experience and want to be part of shaping a new team in Ireland, wed love to hear from you. Apply today with your CV. #LI-DB4 Skills: "Emerson Syncade" "EBR" "Materials" "Weigh & Dispense" "Equipment Tracking" "DeltaV" "MES"

Catalyx is seeking a MES Support Engineer to join our team and work for our newly established team who are based on our customer site in Cork. Who We Are: Catalyx specializes in the science of operational processes. With a footprint across North America and Europe, the company carefully automates and services R&D, production, packaging, and delivery processes-globally-with a sophisticated blend of products, technologies, and lifecycle services. The company was formed in 2022 after CXV Global (Crest Solutions, Xyntek, and VistaLink) and Panacea Technologies joined forces. For over three decades, Catalyx's partnership-based culture has helped organizations in production-intense, highly regulated industries optimize their operational efficiency, performance, and safety. To learn more about the company's experience and comprehensive suite of capabilities and solutions, visit . The Role: Catalyx is a trusted partner in delivering world-class lifecycle services to regulated and high-risk end markets. With a relentless commitment to innovation and excellence, we partner with life science and other highly regulated organisations, to empower them to enhance efficiency, and drive success. As part of this commitment, we are continuously developing our on-site teams to support the advancement of customer operations. Responsibilities: Provide hands-on, onsite support for MES, SAP, and PI interface issues, with direct involvement in troubleshooting at the shop floor level. Troubleshoot MES-related incidents and service requests directly on the production floor, ensuring minimal disruption to operations. Participate in scheduled maintenance and ensure proper documentation of activities. Execute support and sustainment tasks in alignment with business and GMP compliance requirements. Resolve PAS-X-related issues onsite, including visibility of MO/PO, stuck records, peripheral device malfunctions, and general system access or performance concerns. Provide real-time shop floor support to Manufacturing, guiding end users on MES navigation, eBR execution, and optimal system use to promote self-sufficiency. Support change controls, CAPA processes, and integration of new product changes for GMBRs, MBRs, eBRs, and ESP across filling, inspection, and packaging operations. Assist with platform and server maintenance activities as the primary onsite resource, managing system administration and technical support needs. Engage actively with cross-functional project teams to build effective working relationships and ensure successful project execution. Participate in gathering and documenting MES system requirements through client interaction, workflow analysis, and documentation review. Contribute to fit-gap analysis between customer requirements and MES capabilities to inform system customization and enhancement. Support the design and rollout of MES solutions to replace paper-based or manual processes, such as batch records, weigh & dispense, warehouse management, and material tracking. Assist in testing MES systems and ensure readiness for deployment. Requirements: Bachelor's degree in Engineering, Computer Science, Information Systems, or a related field. 3+ years of experience working with MES platforms in a GMP-regulated manufacturing environment. Experience with MES systems such as Werum PAS-X, Rockwell PharmaSuite, or Emerson Syncade is highly desirable. Why Join Catalyx? At Catalyx we understand that our people are our greatest asset. For this reason and many others, we take care of them. The team in Catalyx benefits from a Total Rewards package. This includes great personal benefits and professional growth opportunities. Catalyx is an Equal Opportunity Employer. We are committed to creating a diverse and inclusive workplace where all individuals are valued, respected, and supported. We do not discriminate on the basis of race, colour, religion, sex (including pregnancy, gender identity, and sexual orientation), national origin, age, disability, veteran status, genetic information, or any other characteristic protected by applicable law. We encourage applications from all qualified candidates, regardless of background, and strive to create a welcoming environment for everyone. At Catalyx, we are committed to attracting the best global talent. We proudly support our international employees by offering assistance with Critical Skills Visa applications for eligible candidates. To be considered for this role you will be redirected to and must complete the application process on our careers page. To start the process, click the Apply button below to Login/Register.