Company description: TIRLN LIMITED Job description: Electrical Instrumentation Hit Apply below to send your application for consideration Ensure that your CV is up to date, and that you have read the job specs first. - Apprenticeship 4 year Apprenticeship Programme Belview, Co Kilkenny Tirln Tirln, is a world-class food and nutrition co-operative, with a diverse portfolio of quality ingredients, leading consumer and agri brands. Tirln owns leading brands such as Avonmore, Kilmeaden Cheese, Millac, Solmiko, Truly Grass Fed, Premier Milk, Wexford, and GAIN Animal Nutrition. We nurture a talented team across Ireland, the US, MEA and China, delivering annual revenues of over €3 billion, and over 2,300 people to manage our network of 11 processing plants and 52 agri branches. Our purpose is to nourish the world, while safeguarding our environment for future generations. Role Profile Tirln is offering apprenticeship opportunities to current leaving certificate students and recent school leavers in Belview/Ballyragget. Tirln has a well-established and highly regarded apprenticeship programme, where apprentices will train for 4 years combining practical industrial experience and Solas/ETB run academic training. During this time, youll earn while you learn and receive mentorship from craft professionals at Tirln. As an apprentice, you will: Maintain site process equipment, including utilities. Process equipment includes various types of motors, pumps, valves, fans, chart recorders, process instrumentation and packaging systems. Replace and repair defective mechanical & electrical equipment, instruments, and cabling when necessary. Carry out all operations to conform to GMP requirements. Adhere to all health and safety policies and procedures, including the use of the appropriate protective clothing. Under senior craft supervision you will carry out scheduled Preventative Maintenance (PMs) on process and utilities equipment - Working on fault find/troubleshooting with equipment such as flow meters, control valves, temperature transmitters, VSDs, Profibus, SCADA systems, pasteurisers, evaporators, drying systems, material transport systems and utility systems as part of a team and as an individual. Liaise with all Maintenance, Manufacturing, Project, Quality and any other site personnel, to meet the site objectives. Provide feedback on equipment and spares issues. Fill out all required paper work such as PM documentation, Lockout Tagout permit book and adhere to all site protocols. Inform maintenance lead, shift manager or any relevant site personnel of impact of work being carried out and results of any issues that may arise. Provide accurate reporting as necessary, including the use of computer maintenance system (CMMS SAP). Requirements Legal age limit Candidates must be 16 years or over Educational standard Grade D or higher in 5 subjects at Leaving Certificate level Enjoys problem solving Team player Task orientated Takes direction well to uphold Tirlns robust health & safety standards Flexible and adaptable Benefits Varied work in fast paced manufacturing environment Career progression opportunities Opportunity to earn while your learn Closing date for applications: 30th April 2026 Commitment to Diversity & Inclusion We believe in the value of difference. We know that different perspectives, life experience and backgrounds can drive innovation and deliver growth. xsokbrc We welcome people from all walks of life without regard to race, colour, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, or disability status. Join our Talent Pool Considering a new career in Tirln but this isnt the role for you? Join our talent community and sign up for job /careers Tirln is a Values Based Organisation Profile description: Legal age limit Candidates must be 16 years or over Educational standard Grade D or higher in 5 subjects at Leaving Certificate level Enjoys problem solving Team player Task orientated Takes direction well to uphold Tirlns robust health & safety standards Flexible and adaptable Skills: Trade Electrical Apprenticeship

Supply Chain Planner (12 Month Contract) Our client, a leading medical device manufacturer here in Waterford are seeking a Supply Chain Planner to join their team. The following information aims to provide potential candidates with a better understanding of the requirements for this role. The successful candidate will be responsible for planning, scheduling, inventory and may perform work in a specific sub-specialty in Inventory Planning and Control or Operations. Key Responsibilities (Essential responsibilities include but are not limited to the following): Responsible for inventory replenishment based on production schedules, current inventory, customer orders and forecasts. Responsible for planning, scheduling, coordinating and giving final approval of the master schedule of products through the complete production cycle. Liaise with stakeholders to reschedule production to support business. Support business execution of new programs and initiatives. Monitor key performance indicators, analyses cost and coordinate cross functional work teams to increase effectiveness of supply chain initiatives. Assist with development of metrics to assess and improve forecast accuracy. Assist with the development and implementation of department standards, practices, procedures and policies to ensure the accuracy of inventory records. Supports all company safety and quality programs and initiatives. Ensure ongoing compliance with GMP in all practices, recording of events and processes. Ensure compliance with all learnings from all GMP training events. Other responsibilities may be assigned from time to time as needed, based on the evolution of the company and the requirements of the department/position. Job Specifications: The minimum education and experience required to perform this job competently. Degree Qualified, highly desirable, with specific or additional qualifications in the area of supply chain management, logistics and/or planning including an APICS, CPIM or APICS CSCP certification. At least 2 -3 years experience of supply planning preferably within a Healthcare/ Pharmaceutical environment. Strong understanding of forecasting, MPS, and MRP. Strong understanding of Pharmaceutical RA / GMP compliance. xsokbrc Experience of SAP desirable. Skills/Attributes: Can work in a fast-paced manufacturing environment Excellent problem solver Target Driven Self-Motivated Ability to Multitask Skills: Supply chain planning Production Planning Inventory Management Supply Planning

The Maintenance Technician will carry out production, plant, lab and facility maintenance activities. Do not wait to apply after reading this description a high application volume is expected for this opportunity. This role will also require the maintenance technician to take part in process development of new products & processes, production troubleshooting, process validation and equipment validation, as deemed necessary. Principal Responsibilities: Carry out maintenance activities. Develop Maintenance Procedures in conjunction with the process engineer or process engineering manager. Comply with procedures as defined by plant SOPs. Carry out project work, as deemed necessary. Participate in equipment and facility validations, as necessary. Contribute to development of engineering systems through continuous improvement. Key cGMP Responsibilities To maintain the lab, plant and production equipment to the required standards. To maintain the engineering systems in a compliant manner. To document such activities as described above in the required manner. Follow Standard Operating Procedures whilecarrying out maintenance activities at all times. Follow Gowning Procedures and entry rules for all manufacturing and other controlled areas. Understand and follow Personal Hygiene Rules as defined in the GMP Training Programme and notify area supervision of any health conditions which may affect the quality of product. Participate fully in all GMP and operational training programs and complete all Training records in an accurate and timely manner. Maintain work areas in a clean and tidy manner at all times. Requirements Recognised mechanical or electrical qualification (e.g. National Craft Certificate) Experience in a medical device or pharmaceutical industry highly desirable. Working knowledge of PLC and pneumatics systems. xsokbrc Strong electro-mechanical background and knowledge of automated systems. Skills: Electrical Mechanical Maintenance Planned maintenance

Leo Lynch Waterford, County Waterford, Ireland 2 days ago Be among the first 25 applicants About Us Since the 1950s, Leo Lynch has been providing the pharmaceutical, semiconductor, industrial, food, commercial and retail industries with professional project management and high caliber craftsmanship. At Leo Lynch, we build and manage complex engineering & construction projects for the world’s leading corporations. Our solutions help deliver technologies that connect people, communities and businesses, giving them the power to achieve incredible things. Leo Lynch employs the best people, invests heavily in training and education, and ensures that the highest standards of health, safety and governance are applied throughout the organisation. About The Role Reporting to the Estimating Manager and as an integral part of the estimating team, you will be responsible for preparing accurate mechanical cost estimates ensuring timely submission of tenders. You will become proficient in the use of cost estimating software with training provided. You will work on tenders for projects such as Pharmaceutical, Food & Beverage, Data Centers, Semi-Conductor, Commercial, etc across Ireland and the UK. Responsibilities Conduct in-dept reviews of tender documents, drawings, specifications, schedules, etc Ensure quantity take-offs and mark up measured drawings are accurately prepared Request, manage and evaluate supplier and sub-contractor quotations Issue tender queries and RFIs Prepare costed bill of quantities Prepare tender reports, tender pricing schedules and other tender return documents Advise on potential value engineering opportunities Manage data base Attend meetings and site visits are when required Adhere to tender return deadlines Liaise with clients, consultants, contractors, and wider project teams Other related tasks as instructed Candidate Requirements Degree in either Mechanical, Process, Building Services Engineering or other related field 10+ years of previous mechanical cost estimating experience in a contracting environment with experience of delivering tenders from enquiry to award stage is essential Strong computer skills especially in the use of MS Office Strong understanding of mechanical & process pipework systems, HVAC, plumbing and other mechanical building services systems Good knowledge of different mechanical & process pipework materials Strong attention to detail Ability to interpret drawings and specifications, preform accurate take-offs, and prepare detailed BOQs Ability to manage own workload and meet deadlines Must display excellent time management, communication, numerical, analytical and organisational skills Problem solving skills with attention to detail and multitasking abilities Seniority level Mid-Senior level Employment type Full-time Job function Management and Manufacturing Industries Construction Referrals increase your chances of interviewing at Leo Lynch by 2x Get notified about new Senior Estimator jobs in Waterford, County Waterford, Ireland . #J-18808-Ljbffr

Location: On site / Waterford, Ireland Job type: Permanent / Full-time Sector and subsector: Engineering | Mechanical Salary: Competitive Salary About Us: Since the 1950s, Leo Lynch has been providing the pharmaceutical, semiconductor, industrial, food, commercial and retail industries with professional project management and high caliber craftsmanship. At Leo Lynch, we build and manage complex engineering & construction projects for the world’s leading corporations. Our solutions help deliver technologies that connect people, communities and businesses, giving them the power to achieve incredible things. Leo Lynch employs the best people, invests heavily in training and education, and ensures that the highest standards of health, safety and governance are applied throughout the organisation. About the Role: Reporting to the Estimating Manager and as an integral part of the estimating team, you will be responsible for preparing accurate mechanical cost estimates ensuring timely submission of tenders. You will become proficient in the use of cost estimating software with training provided. You will work on tenders for projects such as Pharmaceutical, Food & Beverage, Data Centers, Semi-Conductor, Commercial, etc across Ireland and the UK. Responsibilities: Conduct in-dept reviews of tender documents, drawings, specifications, schedules, etc Ensure quantity take-offs and mark up measured drawings are accurately prepared Request, manage and evaluate supplier and sub-contractor quotations Issue tender queries and RFIs Prepare costed bill of quantities Prepare tender reports, tender pricing schedules and other tender return documents Advise on potential value engineering opportunities Attend meetings and site visits as required Adhere to tender return deadlines Liaise with clients, consultants, contractors, and wider project teams Other related tasks as instructed Candidates Requirements: Degree in either Mechanical, Process, Building Services Engineering or other related field 10+ years of previous mechanical cost estimating experience in a contracting environment with experience of delivering tenders from enquiry to award stage is essential Strong computer skills especially in the use of MS Office Strong understanding of mechanical & process pipework systems, HVAC, plumbing and other mechanical building services systems Good knowledge of different mechanical & process pipework materials` Strong attention to detail Ability to interpret drawings and specifications, perform accurate take-offs, and prepare detailed BOQs Ability to manage own workload and meet deadlines Must display excellent time management, communication, numerical, analytical and organisational skills Problem solving skills with attention to detail and multitasking abilities #J-18808-Ljbffr

A leading nutrition company is seeking a VAT Specialist for a 12-month FTC to cover maternity leave. This role involves preparing VAT returns, ensuring compliance with regulations, and supporting cross-border transactions. Candidates should be AITI or ACA/ACCA qualified with a strong understanding of VAT legislation and experience in tax compliance. Hybrid working arrangements are available in Ireland, providing flexibility for work-life balance. #J-18808-Ljbffr

Overview This post represents an exciting opportunity to work with an experienced multidisciplinary team based primarily in Clontarf. The role will provide clinical, educational and research guidance and support to colleagues in the CRC and to referrers nationwide. Responsibilities Provide clinical guidance and support to colleagues in the CRC and referrers nationwide. Evaluate and disseminate evidence‑based practice in gait and movement analysis. Influence clinical practice through research guidance. Location and Position Details Waterford Part‑time (Specified Purpose) Grade: Clinical Nurse Manager 1 2127 Category: Nursing and Midwifery Contact Grainne DePaor, CDNM Waterford (051) 312692 e‑mail: gdepaor@crc.ie #J-18808-Ljbffr

MSAT Visual inspection lead page is loaded## MSAT Visual inspection leadlocations: Waterford: Val-de-Reuil: Le Trait: Marcy-l'Etoile: Frankfurt am Maintime type: Vollzeitposted on: Heute ausgeschriebentime left to apply: Enddatum: 26. April 2026 (Noch 18 Tage Zeit für Bewerbung)job requisition id: R2850616**MSAT Visual Inspection Lead*** *Location: Site based from Waterford, Val-De-Reuil, Le Trait, Frankfurt or other Drug Product Site in Sanofi*About the job**Our Team:**We are an R&D-driven, AI-powered biopharma company with one unwavering purpose: **to chase the miracles of science and improve people's lives.**Our deep understanding of the immune system — combined with an innovative and growing pipeline — enables us to invent medicines and vaccines that treat and protect millions of people worldwide. At Sanofi, we believe that progress is powered by people: bold thinkers, collaborative leaders, and passionate scientists who dare to push boundaries every day.**Join us. And help change the world.**This is a great opportunity to shape the future of Visual Inspection (VI) on a global scale.As the **Global MSAT Visual Inspection Lead**, you will be at the heart of Sanofi's injectable manufacturing excellence — driving the strategy, standardization, and innovation of visual inspection programs across a network of drug product sites in three Global Business Units (GBUs). You will lead a team of VI experts, champion cutting-edge inspection technologies and processes, and serve as the authoritative voice connecting Manufacturing Science, Analytics & Technology (MSAT) with Global Quality, Engineering, Procurement, and Business Strategy.This is more than a technical leadership role — it is a platform to **inspire teams, influence industry practices, and deliver meaningful impact for patients worldwide.****Main responsibilities:**• Lead the Global Visual Inspection program as MSAT authority, serving as a strategic partner in Sanofi's enterprise-wide VI strategy while aligning Global Quality, Global Engineering, Procurement, Business Strategy, and injectable manufacturing sites on all VI-related topics.• Build, lead, and develop a high-performing team of VI experts distributed across 8 sites, providing specialist support across the full Drug Product injectable network.• Drive global harmonization of VI strategy and implementation across Manual (MVI), Semi-Automated (SAVI), and Automated (AVI) inspection modalities for vials, pre-filled syringes, and cartridges.• Deliver expert technical guidance on defect classification, VI recipe optimization, particulate control, false reject rate reduction, robotics, and layered inspection technologies, ensuring holistic VI lifecycle management.• Lead the evaluation and acquisition of new VI lines and emerging technologies, ensuring full alignment with quality, regulatory, and operational requirements across the network.• Champion innovation and industry benchmarking by identifying cost-effective inspection solutions and actively engaging with PDA, Biophorum, A3P, and other industry bodies to define and disseminate best practices across the organization.• Ensure full regulatory compliance and good documentation practices while providing structured mentorship and knowledge transfer to develop VI capability across new and existing associates.**About you*** *Proven background in injectable manufacturing within a cGMP environment, with dedicated expertise in visual inspection and a track record of leadership and impact** *Demonstrated experience in transformation programs, technology transfer, validation, and manufacturing support**Qualifications** *Advanced degree in a scientific discipline** *Deep knowledge of GMP, CMC requirements, and current regulatory guidance and best practices in visual inspection, as defined by global health authorities** *Experience preparing and reviewing regulatory dossiers with direct health authority interactions**Skills & Competencies** *Exceptional leadership presence — able to inspire, influence, and align cross-functional and multicultural teams without direct authority** *Outstanding communication skills, with the confidence to engage senior stakeholders and represent Sanofi in external industry forums** *Proven ability to operate autonomously in complex, matrixed, and international environments**Operational & Language** *Fluency in English required; proficiency in an additional European language is a valued asset** *Flexibility to provide occasional off-shift support, remotely or on-site, as operational needs require*Diversity und Inklusion sind in den Grundwerten von Sanofi verankert und spiegeln sich in unserer Arbeitsweise wider. Wir respektieren die Vielfalt unserer Belegschaft in Hinsicht auf ihre Herkunft, Erfahrungen und Lebensweisen. Wir erkennen die Bereicherung, die diese Vielfalt birgt, und fördern Inklusion sowie eine Arbeitsumgebung, in der diese Unterschiede sich weiter entwickeln können, zur Stärkung des Lebens unserer Mitarbeiter, Patienten und Kunden. #J-18808-Ljbffr

MSAT Visual inspection lead page is loaded## MSAT Visual inspection leadlocations: Waterford: Val-de-Reuil: Le Trait: Marcy-l'Etoile: Frankfurt am Maintime type: Full timeposted on: Posted Todaytime left to apply: End Date: April 26, 2026 (18 days left to apply)job requisition id: R2850616**MSAT Visual Inspection Lead*** *Location: Site based from Waterford, Val-De-Reuil, Le Trait, Frankfurt or other Drug Product Site in Sanofi*About the job**Our Team:**We are an R&D-driven, AI-powered biopharma company with one unwavering purpose: **to chase the miracles of science and improve people's lives.**Our deep understanding of the immune system — combined with an innovative and growing pipeline — enables us to invent medicines and vaccines that treat and protect millions of people worldwide. At Sanofi, we believe that progress is powered by people: bold thinkers, collaborative leaders, and passionate scientists who dare to push boundaries every day.**Join us. And help change the world.**This is a great opportunity to shape the future of Visual Inspection (VI) on a global scale.As the **Global MSAT Visual Inspection Lead**, you will be at the heart of Sanofi's injectable manufacturing excellence — driving the strategy, standardization, and innovation of visual inspection programs across a network of drug product sites in three Global Business Units (GBUs). You will lead a team of VI experts, champion cutting-edge inspection technologies and processes, and serve as the authoritative voice connecting Manufacturing Science, Analytics & Technology (MSAT) with Global Quality, Engineering, Procurement, and Business Strategy.This is more than a technical leadership role — it is a platform to **inspire teams, influence industry practices, and deliver meaningful impact for patients worldwide.****Main responsibilities:**• Lead the Global Visual Inspection program as MSAT authority, serving as a strategic partner in Sanofi's enterprise-wide VI strategy while aligning Global Quality, Global Engineering, Procurement, Business Strategy, and injectable manufacturing sites on all VI-related topics.• Build, lead, and develop a high-performing team of VI experts distributed across 8 sites, providing specialist support across the full Drug Product injectable network.• Drive global harmonization of VI strategy and implementation across Manual (MVI), Semi-Automated (SAVI), and Automated (AVI) inspection modalities for vials, pre-filled syringes, and cartridges.• Deliver expert technical guidance on defect classification, VI recipe optimization, particulate control, false reject rate reduction, robotics, and layered inspection technologies, ensuring holistic VI lifecycle management.• Lead the evaluation and acquisition of new VI lines and emerging technologies, ensuring full alignment with quality, regulatory, and operational requirements across the network.• Champion innovation and industry benchmarking by identifying cost-effective inspection solutions and actively engaging with PDA, Biophorum, A3P, and other industry bodies to define and disseminate best practices across the organization.• Ensure full regulatory compliance and good documentation practices while providing structured mentorship and knowledge transfer to develop VI capability across new and existing associates.**About you*** *Proven background in injectable manufacturing within a cGMP environment, with dedicated expertise in visual inspection and a track record of leadership and impact** *Demonstrated experience in transformation programs, technology transfer, validation, and manufacturing support**Qualifications** *Advanced degree in a scientific discipline** *Deep knowledge of GMP, CMC requirements, and current regulatory guidance and best practices in visual inspection, as defined by global health authorities** *Experience preparing and reviewing regulatory dossiers with direct health authority interactions**Skills & Competencies** *Exceptional leadership presence — able to inspire, influence, and align cross-functional and multicultural teams without direct authority** *Outstanding communication skills, with the confidence to engage senior stakeholders and represent Sanofi in external industry forums** *Proven ability to operate autonomously in complex, matrixed, and international environments**Operational & Language** *Fluency in English required; proficiency in an additional European language is a valued asset** *Flexibility to provide occasional off-shift support, remotely or on-site, as operational needs require*# Pursue *progress*, discover *extraordinary*Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.Watch our and check out our Diversity Equity and Inclusion actions at ! #J-18808-Ljbffr

Eine biopharmazeutische Firma mit Sitz in Waterford sucht einen erfahrenen Global MSAT Visual Inspection Lead, der die globale Strategie für visuelle Inspektion leitet und ein Team von Experten aufbaut. Der ideale Kandidat hat umfangreiche Kenntnisse in der Herstellung von Injektabilia und der Einhaltung von cGMP-Richtlinien. Diese vielseitige Rolle umfasst die Leitung von Innovationsprogrammen, die Harmonisierung von Prozessen über mehrere Standorte und die Sicherstellung der regulatorischen Compliance. Das Unternehmen strebt nach Spitzenleistung in der Arzneimittelproduktion und fördert eine inklusive Arbeitsumgebung. #J-18808-Ljbffr