4 Mes Engineer 1544 jobs in Ireland

MES Engineer 1544

Limerick, Munster SimoTech

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+353-21-4834930 Specialists in Life Science Automation and IT Systems

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SimoTech provides manufacturing automation and IT systems engineering, project management and validation services. We partner with life sciences companies to design, build, operate and optimise critical process automation systems that deliver fast track project delivery, operational efficiency, improve manufacturing agility and achieve regulatory compliance.

Why SimoTech

What is it like to work at SimoTech? With a strong collaborative teamwork culture based on respect, trust and excellence, we play a critical partnering role to our clients’ life-changing supply of products to patients. In return, there is excellent salary, career progression, educational support and much more.

SimoTech has a new opportunity for an experienced MES Engineer to join our team supporting a global pharmaceutical organisation onsite in Limerick. This is an exciting opportunity where you will gain exposure to next generation manufacturing, delivering improvements in safety and quality, as well as increased productivity and process performance.

This role will support the business processes and systems for a greenfield manufacturing site which will include advanced data collection and analysis platforms. In particular, you will provide MES analyst support for an integrated set of systems that includes Syncade, DeltaV and SAP.

Key Responsibilities
  • Support site readiness activities to enable site start-up and ongoing operations.
  • Configures MES Syncade to support technical testing and installation with appropriate users and systems personnel.
  • Work with local and global IT groups to support delivery of manufacturing solutions.
  • Analyses business processes and needs to recommend or implement changes to systems and/or procedures.
  • Performs user requests for special support and/or extracts of data.
  • Works in all phases of systems development cycle (define, design and deliver solution) according to company and department guidelines.
  • Ensure compliance with Computer Systems Validation policies, standards, procedures and/or practices.
  • Assists Systems Operations, Desktops and/or telecommunications personnel on application of fixes and related troubleshooting.
  • Identify root cause and action plan to avoid the same situation occurs.
Qualifications
  • Bachelor’s Degree in Information Technology, Computer Science, Engineering or related field.
  • At least 7 yearsrelevant Automation experience.
  • Pharmaceutical industry experience, supporting Emerson Syncade systems.
  • High proficiency in integrating Syncade with key manufacturing systems such as DeltaV and SAP.
  • Computer Systems Validation in cGMP regulated operations experience.
  • Knowledge of System Development Life Cycle.
  • Ideally 5 days on site but possibly 3 days minimum.
What SimoTech Can Offer
  • Role provides a high degree of autonomy to allow the successful candidate to reach their full potential.
  • Develop new skills and enhance technical ability by working with innovative technologies in a multi-disciplined environment.
  • Opportunity to work with large corporate clients on exciting capital projects.

By submitting my data (CV), I consent to SimoTech collecting and storing my personal data, as outlined in the SimoTech Privacy Statement which I have read.

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MES Engineer - Syncade

Dublin, Leinster Cognizant Technology Solutions Ireland

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Cognizant is looking for dedicated, innovative and driven talent to join our expanding team in Dublin. We're currently looking for a full-time MES Engineer, and the role comes with a generous salary and benefits package. As an MES Engineer, you will be responsible for implementing System/MES recipe changes and managing the day-to-day issues that arise in the support of Electronic Batch Records, Weigh and Dispense and Equipment Management modules on ourEmerson Syncade MES solution. In your first few weeks in this role, you can expect to: Maintain the incident queue in Service Now and manage and resolve issues as they arise in a timely manner Initiate and implement change control activities in accordance with quality standards and practices Investigate and troubleshoot problems which occur and determine solutions or recommendations for changes and/or improvements Prioritise support activities in line with project schedules. To apply for this MES Engineer role, you will need a minimum of 3 years of experience supporting IT applications, e.g. troubleshooting, managing incidents and change controls, design documentation, test case development, system and integration testing. You will also require the following: Create business process flow diagram for pharmaceutical product recipes based on the paper batch record or source documents. Gather MES Site specific requirement analysis to develop URS and FRS. Logically breakdown the recipes Mfg. process to configure the recipe in to Werum PAS-X Develop/create MBR design elements (building blocks) and workflows in Werum PAS-X for repetitive use in MBR creation to expedite the process. Gather master data and configure in Werum PAS-X Development/Quality/Production Environment. Integrating Werum PAS- X with SAP and other automation systems using standard interface component of MBR design. Lead the recipe design session with business process SMEs. Design MBR/recipe equipment workflow/ status diagram based on the Business process flow. Create solution design and configuration document. Prepare key user training documents and impart key user training. Provide assistance in business SOP creation. A Bachelors degree in Computer Science Computer Engineering Computer Information Systems or a related field (Technology Management Chemical Engineering) Intermediate level Werum PAS-X experience desired Werum PAS-X product hands-on experience for Full application configurations including interface with SAP and automation systems. In-depth of knowledge of Bio Pharma processes Creation of business process flow diagram Master Batch Record creation in Werum PAS-X Knowledge on Industry Standards S88 and ISA S95 Pharmaceutical validation concept cGMP and GDP standards and GAMP Standards Good verbal written communication At Cognizant, taking care of employees is a priority: You can pursue innovative career tracks and opportunities here You can enhance your professional development through education and dedicated training Well give you the skills you need to keep pace with the changing workplace while our compensation, benefits and wellness packages help you stay healthy and plan for the future. Please reach out to our friendly and welcoming team today to apply for this full-time hybrid MES Support Engineer position in Dublin. . At Cognizant, we engineer modern businesses to improve everyday life. Because we're dedicated to making a lasting impact. Cognizant (Nasdaq-100: CTSH) is one of the world's leading professional services companies, transforming clients' business, operating and technology models for the digital era. Our unique, industry-based, consultative approach helps clients envision, build, and run more innovative and efficient businesses. Skills: MES Syncade PAS-X MBR URS FRS Batch Record
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Senior MES Engineer (Pharma)

Ballina, Connacht Gertek Project Management

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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.
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Senior MES Engineer (Emerson Syncade)

Limerick, Munster Cpl Resources

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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"
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MES Support Engineer

Cork, Munster Catalyx

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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.
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