16 Mes Engineer 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.

Innovation starts from the heart. Edwards Lifesciences is the leading global structural heart innovation company, driven by a passion to improve patient lives. With millions of patients served in over 100 countries, each team makes a meaningful contribution by improving patient outcomes and discovering lasting solutions for unmet patient needs. Our Engineering Automation position is a unique career opportunity that could be your next step towards an exciting future.
The Director of Engineering will develop and drive Process Automation in providing technical expertise in the design, prototyping, assembly, development, and troubleshooting of innovative automation system in partnership with R&D and NPD groups. Continuing to innovate and improve by extracting more opportunities and benefit from automation technology.
**How you'll make an impact:**
+ Initiate and lead the design, prototyping, assembly, development, and troubleshooting of highly complex automation systems in support of R&D, New Product Development / Introduction, instilling DFM.Lead in identifying risk, developing mitigation strategies, alternative solutions, resolving issues, etc. in collaboration with cross functional groups and key stakeholders.Oversee, inspire, and develop SMEs, and retain a technical talent to ensure automation knowledge continuity and knowledge

Innovation starts from the heart. Edwards Lifesciences is the leading global structural heart innovation company, driven by a passion to improve patient lives. With millions of patients served in over 100 countries, each team makes a meaningful contribution by improving patient outcomes and discovering lasting solutions for unmet patient needs. Our Engineering Automation position is a unique career opportunity that could be your next step towards an exciting future.
The Senior Automation Engineer provides technical Support in the development of a complex automation system, driving cross functional alignment and ensuring robust, compliant and efficient manufacturing process.
**How you'll make an impact:**
+ Development of bespoke automation solutions based on technology roadmap, with ownership for funding proposals, initial design, development of proof of concept, system testing, solution provider/supplier selection and management, and rollout of automation solution to other sites. Experience in the space of robotics, vision and electrical preferred
These tasks support the design, prototyping, assembly, and development of automation of existing processes and mechanical components.
+ Support the design activities, analysis, modification, and integration of robotics, automation technologies, and processes related to equipment. Ensures applicability to programs and products, handling high complexities
+ Complete proposals for funding of automation solutions for internal and external audiences
+ Collaborate with cross-functional partners to conduct complex technical experiments, research, and design various prototypes to achieve consensus and make informed technical decisions.
+ Lead improvement activities within internal or external teams, or manufacturing processes to drive enhancements and improve efficiency. Utilize metrics to perform continuous improvement.
+ Support the development and influence multiple development teams and various technical domains to support and drive improvements and changes.
+ Establish and enforce engineering standards, best practices, and methodologies to ensure efficiency and quality engineering results.
**What you'll need (Required) :**
+ Bachelor's Degree in Engineering or a Scientific field, and a minimum of 4 years experience working in automation domain (robotics/vision or electrical experience preferred)
**What else we look for (Preferred) :**
+ Whichever applicable, expert skills (with years of proven record) in mechanical design, or programming skills (PLC, Robotics, or vision), or electrical design
+ Demonstrates proficiency in creating excellent technical documentation, white papers, and technical write-ups
+ Ability to translate technical information to all levels of the organizations
+ Capable of delivering effective presentations on complex technical information and project activities
+ Knowledge of applicable FDA regulations for medical device industry is a plus
+ Substantial understanding of processes and equipment used in assigned work
+ Extensive knowledge and understanding of principles, statistic, theories, and concepts relevant to Engineering
+ Advanced problem-solving, organizational, analytical and critical thinking skills with proven record
+ Strict attention to detail
+ Ability to manage competing priorities in a fast-paced environment, including the ability to manage vendors and project stakeholders
+ Excellent communication skills and interpersonal relationship skills including negotiating and relationship management skills
+ Must be able to work in a team environment, including frequent inter-organizational and outside customer contacts
+ Represents organization in providing solutions to difficult technical issues associated with specific projects
+ Adhere to all company rules and requirements (e.g., pandemic protocols, Environmental Health & Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control
+ Ability to interact professionally with all organizational levels
+ Demonstrates strong technical leadership, influences multiple development teams and various technical domains, supports and drives company improvements and changes.

Innovation starts from the heart. Edwards Lifesciences is the leading global structural heart innovation company, driven by a passion to improve patient lives. With millions of patients served in over 100 countries, each team makes a meaningful contribution by improving patient outcomes and discovering lasting solutions for unmet patient needs. Our Engineering Automation position is a unique career opportunity that could be your next step towards an exciting future.
The Principal Automation Engineer provides technical leadership in the development of complex automation system, driving cross functional alignment and ensuring robust, compliant and efficient manufacturing process.
**How you'll make an impact:**
+ Development of bespoke automation solutions based on technology roadmap, with ownership for funding proposals, initial design, development of proof of concept, system testing, solution provider/supplier selection and management, and rollout of automation solution to other sites. Experience in the space of robotics, vision and electrical preferred
These tasks support the design, prototyping, assembly, and development of automation of existing processes and mechanical components.
+ Lead the design activities, analysis, modification, and integration of robotics, automation technologies, and processes related to equipment. Ensures applicability to programs and products, handling high complexities
+ Complete proposals for funding of automation solutions for internal and external audiences
+ Lead collaboration with cross-functional partners to conduct complex technical experiments, research, and design various prototypes to achieve consensus and make informed technical decisions.
+ Lead improvement activities within internal or external teams, or manufacturing processes to drive enhancements and improve efficiency. Utilize metrics to perform continuous improvement.
+ Train, coach, and guide junior/senior engineer on complex technical task. Review works and may direct others to supervise.
+ Lead the development and influence multiple development teams and various technical domains to support and drive improvements and changes.
+ Establish and enforce engineering standard, best practices, and methodologies to ensure efficiency and quality engineering results.
**What you'll need (Required) :**
+ Bachelor's Degree in Engineering or a Scientific field, and a minimum of 6 years experience working in automation domain (robotics/vision or electrical experience preferred)
**What else we look for (Preferred) :**
+ Whichever applicable, expert skills (with years of proven record) in mechanical design, or programming skills (PLC, Robotics, or vision), or electrical design
+ Demonstrates proficiency in creating excellent technical documentation, white papers, and technical write-ups
+ Ability to translate technical information to all levels of the organizations
+ Capable of delivering effective presentations on complex technical information and project activities
+ Knowledge of applicable FDA regulations for medical device industry is a plus
+ Substantial understanding of processes and equipment used in assigned work
+ Extensive knowledge and understanding of principles, statistic, theories, and concepts relevant to Engineering
+ Advanced problem-solving, organizational, analytical and critical thinking skills with proven record
+ Strict attention to detail
+ Ability to manage competing priorities in a fast-paced environment, including the ability to manage vendors and project stakeholders
+ Excellent communication skills and interpersonal relationship skills including negotiating and relationship management skills
+ Must be able to work in a team environment, including frequent inter-organizational and outside customer contacts
+ Represents organization in providing solutions to difficult technical issues associated with specific projects
+ Adhere to all company rules and requirements (e.g., pandemic protocols, Environmental Health & Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control
+ Ability to interact professionally with all organizational levels
+ Demonstrates strong technical leadership, influences multiple development teams and various technical domains, supports and drives company improvements and changes.

Innovation starts from the heart. Edwards Lifesciences is the leading global structural heart innovation company, driven by a passion to improve patient lives. With millions of patients served in over 100 countries, each team makes a meaningful contribution by improving patient outcomes and discovering lasting solutions for unmet patient needs. Our Engineering Automation position is a unique career opportunity that could be your next step towards an exciting future. The Senior Automation Engineer provides technical Support in the development of a complex automation system, driving cross functional alignment and ensuring robust, compliant and efficient manufacturing process. How you'll make an impact: Development of bespoke automation solutions based on technology roadmap, with ownership for funding proposals, initial design, development of proof of concept, system testing, solution provider/supplier selection and management, and rollout of automation solution to other sites. Experience in the space of robotics, vision and electrical preferred These tasks support the design, prototyping, assembly, and development of automation of existing processes and mechanical components. Support the design activities, analysis, modification, and integration of robotics, automation technologies, and processes related to equipment. Ensures applicability to programs and products, handling high complexities Complete proposals for funding of automation solutions for internal and external audiences Collaborate with cross-functional partners to conduct complex technical experiments, research, and design various prototypes to achieve consensus and make informed technical decisions. Lead improvement activities within internal or external teams, or manufacturing processes to drive enhancements and improve efficiency. Utilize metrics to perform continuous improvement. Support the development and influence multiple development teams and various technical domains to support and drive improvements and changes. Establish and enforce engineering standards, best practices, and methodologies to ensure efficiency and quality engineering results. What you'll need (Required) : Bachelor's Degree in Engineering or a Scientific field, and a minimum of 4 years experience working in automation domain (robotics/vision or electrical experience preferred) What else we look for (Preferred) : Whichever applicable, expert skills (with years of proven record) in mechanical design, or programming skills (PLC, Robotics, or vision), or electrical design Demonstrates proficiency in creating excellent technical documentation, white papers, and technical write-ups Ability to translate technical information to all levels of the organizations Capable of delivering effective presentations on complex technical information and project activities Knowledge of applicable FDA regulations for medical device industry is a plus Substantial understanding of processes and equipment used in assigned work Extensive knowledge and understanding of principles, statistic, theories, and concepts relevant to Engineering Advanced problem-solving, organizational, analytical and critical thinking skills with proven record Strict attention to detail Ability to manage competing priorities in a fast-paced environment, including the ability to manage vendors and project stakeholders Excellent communication skills and interpersonal relationship skills including negotiating and relationship management skills Must be able to work in a team environment, including frequent inter-organizational and outside customer contacts Represents organization in providing solutions to difficult technical issues associated with specific projects Adhere to all company rules and requirements (e.g., pandemic protocols, Environmental Health & Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control Ability to interact professionally with all organizational levels Demonstrates strong technical leadership, influences multiple development teams and various technical domains, supports and drives company improvements and changes. 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 Continue to Application or Login/Register to apply button below.