About the Job We are working with a large MNE, who are based in Waterford and are looking to hire a strong ambitious financial accountant to join their team. If you would like to know a bit more about this opportunity, or are considering applying, then please read the following job information. The finance team are very high-performing and have a culture based on fun, togetherness and a desire to continuously improve. This is an exciting role for someone who is ambitious and has a desire to build their career in a Irish MNE Key Responsibilities: Prepare financial statements for the relevant entities that you will support; Prepare reports, KPI analysis, and presentations for stakeholders Run the month end, from posting journals through to reconciliations, and providing commentary on movements. Improve processes through automation as the company grows. Skill Required: ACA, ACCA or CIMA qualified with 0-2 years PQE ideally with industry experience, Excellent communication skills and stakeholder management experience. xsokbrc A keen analytical mind who views the Finance Function as a key strategic enabler to support better business outcomes and commercial decision-making.

Summary: Our client, a leading biopharmaceutical organisation based in Waterford, is seeking an Equipment Project Engineer to deliver a portfolio of capital and automation-related projects across manufacturing and operational areas, including biologics, oral dosage, medical devices, laboratories, and packaging. The successful candidate will manage projects end-to-end, ensuring delivery in line with schedule, cost, quality, and scope requirements, while collaborating with cross-functional teams and external partners to support equipment upgrades, system implementations, and operational improvements within a GMP-regulated environment. Responsibilities: Deliver multiple Automation Related projects, primarily virtualisation of servers associated with live production equipment. Deployment will occur in defined shutdowns requiring excellent co-ordination. Management of multiple groups, Global & local ITS teams, Automation, Validation and Production teams along with specialist external contractors. Develop solutions along with Original Equipment Manufacturer (OEM) to upgrade control systems. Provide automation support and expertise in the procurement, build, commissioning and qualification of GMP equipment. Working in team environment on several projects deployed in a phased nature. Deliver on packaging, serialisation & aggregation biopharmaceutical equipment project portfolio within our clients biopharmaceutical operations which include enzyme,monoclonal antibodies(mAbs), oral dosage, medical device, laboratories & packaging operations. Perform procurement, acceptance of equipment & associated infrastructure on behalf of client and report regularly on project status throughout the project lifecycle. Management of end-to-end project lifecycle is key to success. Ensure compliance environmental, health and safety codes practices, approved project KPIs, performance standards and specifications are maintained. Liaise with external and internal customers, suppliers, and vendors to define and deliver right first-time project deployment. Chair and Interaction with assigned project teams to interpret their requirements and ensure approval to align project scope as requested. Assign responsibilities, mentor project team and maintain accurate project planning documentation as defined by the client the stage gate model for project delivery. Communicate effectively with weekly reports to management and senior stakeholders. Support to other project participants to overcome obstacles when they present themselves. Review engineering deliverables, initiate site change controls and associate documentation required by the project life cycle. Responsible for delivering performance metrics for budget, schedule, scope and quality adherence. Qualifications & Experience: Degree in Mechanical, Chemical, Industrial, or a related Engineering discipline (Masters degree or relevant project management certification is advantageous) Minimum 10 years experience in project engineering or project management roles within a regulated environment Strong experience working within a cGMP pharmaceutical or biopharmaceutical environment Proven experience managing capital projects and equipment-related initiatives Strong knowledge of automation systems and control system upgrades Experience supporting equipment procurement, commissioning, and qualification processes

Manufacturing Engineer Lead role in leading medical device manufacturing company based in Waterford City. Leading a small team, reporting to the Moulding Engineering Manager, the overall purpose of this role is to provide technical support to resolve production issues related to machinery and tooling, scrap reduction, and throughput, as well as lead technical problem solving and root cause investigations. Responsibilities include (but are not limited to the following): Provide technical support in resolving production issues related to machine or tool issues, scrap reduction or throughput. Lead technical problem solving and root cause investigations. Coordinate engineering support for Moulding in executing the production plan to meet the customer requirements. Co-ordinate all technical and training activities across the relevant functions within the Moulding Workcell. Liaise with equipment vendors & program management teams as appropriate. Drive continuous improvement projects in process, tooling or operations. Identify trends and process variations as part of establishing a continuous improvement monitoring system. Develop tooling or equipment documentation, update drawings, document maintenance procedures, work instructions as required. Lead and manage a high performing team. Conduct regular performance reviews, coaching and development planning for the team. Assign daily tasks, set clear priorities and ensure accountability for quality of work and timelines. Promote a strong culture of teamwork, ownership and communication within the Moulding Workcell and across the Toolroom. Support all company safety and quality programs and initiatives. Ensure ongoing compliance with GMP in all practices, recording of events (deviations, non-commercials, Change controls etc.) 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. Role will suit:- Honours degree in Mechanical Engineering, Mechatronics, Biomedical Engineering, Applied Physics, Electronic, Electrical Engineering or similar discipline. 3-5 years experience working in a high volume manufacturing environment desirable. Experience in cleanroom procedures and medical moulding desirable Familiar with process set up and validation, including performing process window studies, IQ,OQ,PQ highly desirable. Be able to work well in a team environment. Data Driven Approach, Good data analysis skills. Have excellent oral and written communication skills. Systematic troubleshooting & fault-finding skills. Project management understanding an advantage. Lean Six Sigma skills understanding an advantage. Skills: Manufacturing People Management Quality Management Lean Moulding Benefits: pension healthcare Profit Share wellness program

Vacancy I.D.: 039988 - Assistant Lecturer / Lecturer in Quantity Surveying Contract: Permanent Whole-Time Salary: The gross salary scale applicable to the grade of Assistant Lecturer is €47,101 - €63,735 p.a. (rates effective 01/02/2026). / The gross salary scale applicable to the grade of Lecturer is €68,936- €106,661 p.a. (rates effective 01/02/2026). SETU are seeking a full time assistant lecturer/ lecturer for our existing Quantity Surveying programme within the Department of Architecture & Built Environment. Candidates who have strong academic and practicing experience especially in the area of sustainable building, project management and research are welcome to apply. The appointee will play an active role in the academic direction of courses including teaching, research, academic assessment and academic administration. Application Process: Applications must be made through the online recruitment system on SETU's Vacancies page on the website. Please log onto SETU Vacancies for further details and to apply for this position. Applications will not be accepted by email, any other third-party website or in any other format. Garda Vetting may be required for particular posts. SETU is an equal opportunities employer. #SETU

What You Need to Know: Matrix Recruitment are currently recruiting an Assistant Accountantfor our client based in South-West Waterford. The following information aims to provide potential candidates with a better understanding of the requirements for this role. This is a permanent role with a company with a great company culture offering flexibility to their teams and a hybrid working model (2 days in office per week). Your New Job: Join a friendly, established accountancy practice as an Accounts Technician or Part-Qualified Accountant. In this role, youll support a team handling day-to-day accounting and bookkeeping for a diverse client portfolio. Youll get direct exposure to cloud accounting tools and work collaboratively as part of a professional, growth-oriented team. Key Duties and Responsibilities: Maintain detailed bookkeeping records for clients Process sales and purchase invoices and update financial ledgers Prepare bank, debtor, and creditor reconciliations Assist with management accounts and VAT returns Support with general financial admin and reporting tasks Prepare year-end accounts and financial reports Work with cloud platforms Train and mentor junior team members Prepare corporation and personal tax returns What Are We Looking For?: Accounts Technician qualification or part-qualified accountant (ACA/ACCA or similar) Experience in an accountancy practice Strong double-entry bookkeeping skills Ability to compile year-end accounts to deadlines Familiarity with accounting systems (Xero a plus) Organised, detail-focused, and a strong team player Apply for This Job: Apply for this job now or get in touch with Rena on for more information. Compliance Statement: By applying, you are giving consent for Matrix Recruitment to contact you about this job. We collect your data for recruitment purposes only and will retain it for the duration required as outlined in our privacy policy. All CVs are treated in strict confidence and will not be submitted to any client without your prior knowledge and permission. Please note that due to the high volume of applications, we can only respond to candidates who meet the criteria for the role. xsokbrc We Value Your Trust. Skills: Accounts Technician PQ Accountant Practice Accountant

Join one of Europe's leading food processing companies with locations across Ireland, UK, and continental Europe. If you think you are the right match for the following opportunity, apply after reading the complete description. Our client currently have a vacancy for a Maintenance Electrician to assist in the day to day running and maintenance of the production facility in Waterford. Responsibilities Managing the full electrical works & trouble shooting of the site and equipment. Lead the site preventative electrical programme & manage scheduling. Carry out work orders in a timely and safe manner while maintaining adherence & full compliance with company procedures Responsibility to upload all job details onto a handheld mobile field technology device on completion. The ability to test, inspect and certificate your own installations. Responsibility for explaining system procedures to site management Develop in-depth working knowledge of all sites electrical equipment Complete all work order form & paperwork in full Follow all Health and Safety Rules and Regulations in the Site. To complete training and review of SOPs on compliance Qualifications Your role will see you tackle a wide range of business challenges in a busy Maintenance/Engineering environment. The ideal Candidate will have or demonstrate: A high level of competency in electrical work / electrical engineering, with a minimum of 3 years post apprenticeship experience. Experience of machines & process equipment, controls & automation. Experience in electrical & mechanical installations & maintenance. Can demonstrate good communication, both written & oral skills, which meet the requirements of the job in full. Good mental ability to logically follow a line of thought for problem solving Holds a full driving license. xsokbrc Ability to work on their own initiative, with minimum supervision, as well as part of a team. Has a flexible approach to working hours (shift work, overtime and on call)

Mechanical Maintenance Technician This role requires the Mechanical Maintenance Technician to work closely with production to ensure optimal line performance with a focus on problem solving and preventive maintenance. Experience, qualification, and soft skills, have you got everything required to succeed in this opportunity Find out below. Reporting to Maintenance Manager the main responsibilities associated with this role are as follows; Primary support to the production function working with the electrical technician to optimize performance. Problem solving mechanical issues on the Manufacturing plant. Involved in changeovers and startups on a daily basis. Working closely as part of an integrated production team. Completing preventive maintenance tasks and checks on a daily basis. Preparation for and participation in the weekly preventive maintenance meetings. Working closely with the Maintenance Manager on Maintenance downtime, root cause analysis and problem solving on plant. Ensure as part of the Maintenance team that all controls and agreed preventive maintenance systems are maintained on the plant. Involved in the maintenance of the parts system with the Maintenance Administrator. Involved in Project Management of capital & continuous improvement projects for the company with the Maintenance Manager. Involvement in Supplier meetings. Involved in the review of weekly preventive maintenance plans to ensure compliance to company plan. SKILLS & EXPERIENCE & ATTRIBUTES Minimum 3 Years experience operating in a regulated industry/environment qualified Trades Fitter / mechanic qualifications considered. Excellent PC Skills. Ability to work on own initiative and as part of a team. Ability to work under pressure and to deadlines. Should have good verbal and written communication skills. Demonstrates a logical approach to problem solving. Has a can do attitude. Ability to mix hands on and Hands off tasks. xsokbrc Have a production mind set as part of an integrated team approach. Skills: Mechanical Maintenance Pneumatic System Mechanical Maintenance Engineering Preventive Maintenance Pneumatics

eir Business Talent is recruiting a Qualification & Validation Engineer for our client in Waterford. This is a hybrid rolerequiring onsite presence every Monday or Friday. The position is offered as a 12-month rolling day-rate contract. We are seeking an experiencedQualification & Validation Engineer - Process Performance Qualification to join our Qualification and Validation Team. In this critical role, you will be responsible for leading and executing Process Performance Qualification (PPQ) activities in accordance with client's global quality standards and applicable regulatory requirements. The role supports the successful delivery of process validation lifecycle activities (Stage 1, Stage 2, and Stage 3) for commercial manufacturing, ensuring that processes consistently produce product meeting predetermined specifications and quality attributes. The role works cross-functionally with MSAT, Operations, Quality Control, and Quality Assurance to ensure PPQ readiness, execution, and reporting are delivered to the highest standards, in full compliance with cGMP, FDA, EMA, and ICH guidelines. Main responsibilities: Author, review, and execute PPQ protocols and reports in alignment with global standards and regulatory expectations. Define PPQ strategy including batch numbers, sampling plans, acceptance criteria, and statistical approaches. Contribute to the development and maintenance of the Process Validation Master Plan (PVMP). Support lifecycle management changes requiring PPQ, including technology transfers and post-approval changes. Develop / Participate in risk assessments to evaluate process risks and define appropriate control strategies. Apply risk-based approaches to PPQ study design, sampling strategies, and acceptance criteria justification. Ensure timely closure of PPQ-related deviations and CAPAs prior to and following PPQ execution. Maintain accurate and audit-ready documentation throughout the validation lifecycle. Work closely with MSAT, Manufacturing Operations, Quality Control, and Quality Assurance to ensure alignment on PPQ strategy, execution, and outcomes. Ensure all PPQ activities are conducted in compliance with applicable regulations and guidelines. Support regulatory inspections and internal audits by providing PPQ documentation and technical expertise. Provide training and technical guidance to operations personnel, validation associates, and cross-functional team members involved in PPQ activities. Design and execute Continued Process Verification (CPV) programs. About you Degree in science (e.g. Chemistry, Microbiology or IT preferred) or Engineering (Chemical/Mech/Elec) discipline Minimum 35 years of experience in pharmaceutical manufacturing, process validation, or quality assurance in a regulated GMP environment Demonstrated hands-on experience in Process Performance Qualification (PPQ) design, execution, and reporting Proven track record of authoring and reviewing validation documentation (protocols, reports, deviations, change controls) Natural influencer and works well as part of a multifunctional team. Highly motivated and self-resilient. Adaptable and flexible as well as a pragmatically minded problem solver. Technical skills: Strong understanding of process validation principles and lifecycle approach; Understanding of of cGMP regulations: FDA 21 CFR Parts 210/211, EU GMP Annex 15, FDA Process Validation Guidance (2011) and EMA process validation requirements, Working knowledge of ICH Q8, Q9, Q10, Q11 guidelines Knowledge of statistical methods applied to process validation (e.g., process capability, statistical sampling) Familiarity with qualification of equipment, utilities, and manufacturing systems Experience with deviation management, CAPA, and change control systems Excellent project management capabilities with ability to manage multiple priorities Strong communication skills with ability to influence at all levels of the organization Strategic thinking with focus on balancing compliance requirements with business needs For more information please apply here or contactHarleen Tora/harleen(dot) Ref:EET7945 Candidates must be eligible to work full time and long term in the location specified or currently hold a valid appropriate long term work Visa to apply. eirbusinesstalent, eir business and our clients are equal opportunity employers who seeks to recruit and appoint the best available person for a job regardless of marital / civil partnership status, sex (including pregnancy), age, religion, belief, race, nationality and ethnic or national origin, colour, sexual orientation or disability. eirbusiness talent, eirbusiness and our clients apply all relevant Data Protection laws when processing your Personal Data. If you choose to apply to this opportunity and share your CV or other personal information with eirbusiness talent, eirbusiness and our clients, these details will be held by us in accordance with our privacy policy used by our recruitment team to contact you regarding this or other relevant opportunities at eirbusiness talent and eirbusiness. Skills: Process Performance Qualification process validation lifecycle cGMP regulations Benefits: Work From Home

Job Summary: We are currently seeking an experienced Qualification & Validation Engineer to join a high-performing validation team within a leading pharmaceutical organisation. This is a key role focused on leading Process Performance Qualification (PPQ) activities across the full process validation lifecycle, ensuring manufacturing processes are robust, compliant, and capable of consistently delivering high-quality products in line with global regulatory standards. Responsibilities Lead and execute Process Performance Qualification (PPQ) activities in line with global quality standards and regulatory requirements Author, review, and approve PPQ protocols and reports Define PPQ strategies including batch selection, sampling plans, acceptance criteria, and statistical methodologies Contribute to and maintain the Process Validation Master Plan (PVMP) Support lifecycle validation activities including technology transfers and post-approval changes Perform and contribute to risk assessments to identify process risks and define control strategies Apply risk-based approaches to PPQ design and execution Ensure timely investigation and closure of deviations, CAPAs, and change controls Maintain accurate, audit-ready documentation throughout the validation lifecycle Collaborate cross-functionally with MSAT, Manufacturing, QC, and QA teams Ensure compliance with cGMP, FDA, EMA, and ICH guidelines Support regulatory inspections and internal audits Provide technical guidance and training to cross-functional teams Design and support Continued Process Verification (CPV) programs Requirements Degree in Science (e.g. Chemistry, Microbiology) or Engineering (Chemical, Mechanical, Electrical or similar) 35+ years experience in pharmaceutical manufacturing, validation, or quality within a GMP-regulated environment Hands-on experience in PPQ design, execution, and reporting Proven experience authoring and reviewing validation documentation Strong understanding of process validation lifecycle principles Knowledge of cGMP regulations including FDA 21 CFR Parts 210/211, EU GMP Annex 15, and relevant FDA/EMA guidance Familiarity with ICH Q8, Q9, Q10, and Q11 guidelines Experience applying statistical methods to process validation Understanding of equipment and system qualification Experience with deviation management, CAPA, and change control systems Strong project management and organisational skills Excellent communication skills with the ability to influence stakeholders Collaborative mindset with the ability to work effectively across multifunctional teams Adaptable, solutions-focused, and proactive approach to problem-solving #LI-PC2 Skills: PPQ Process Validation Deviations CAPA PVMP

Toolmaker Supervisor / Toolroom Team Leader in a leading medical devices company based in Waterford City.( This is a Days role Monday to Friday). The overall purpose of this role : Reporting to the Moulding Engineering Manager, The Toolroom Team Leader is responsible for leading and managing all the day-to-day operations within the Toolroom. This role oversees tooling maintenance, repair, validation support, and continuous improvement activities, while ensuring compliance with safety, quality, and GMP requirements. The Toolroom Team Leader acts as the primary liaison between Toolroom and all supporting functions, manages Toolroom personnel, and ensures that tooling activities are executed efficiently, safely, and in line with business priorities.(Day role Mon to Friday) Key Responsibilities and End Results:(Essential responsibilities include but are not limited to the following): Toolroom Operations & Daily Management Coordinate, plan, and prioritize Toolroom work in line with operational requirements, including commercial repairs, PMs, validations, and project/tooling work. Ensure accurate completion of all required paperwork and documentation for tooling activities, including Non-commercial job documentation, Engineering Change Controls, NCMR Investigation Support, Spare parts usage and inventory transactions and Tool repair reports and traceability records Ensure Toolroom activities align with quality, GMP, H&S procedures and support both internal and external Audits or any other visits. Provide timely and clear updates to stakeholders regarding tool status, risks, and actions required. Attend and actively participate in key daily/weekly meetings, including: CAC (Cleanroom Accountability Meeting) Daily Engineering tier meetings Workcell planning meetings (across different WCs) Problem-Solving sessions (A3, RCCA) Project/NPI meetings as required Technical Responsibilities Oversee and support the dismantling, troubleshooting, repair, and reassembly of complex multi-impression mold tools. Review and approve repair strategies, machining approaches, and corrective actions before work starts. Ensure proper evaluation and documentation of steel wear, damage, metrology issues, and tooling concerns. Support Toolmakers with technical guidance and problem-solving during complex repairs. Represent the Toolroom in cross-functional forums, provide updates, raise risks, and support cross-functional decision-making. Drive improvements in tooling reliability by analyzing recurring issues and implementing sustainable corrective actions. Ensure meeting actions relating to Toolroom are captured, assigned, and closed out. Supervise the setup and operation of Toolroom machinery, including lathes, milling machines, EDM, grinders, and ancillary equipment. Ensure equipment is maintained, safe, and operated only by trained personnel. Support apprentice and Toolmaker training on tooling practices and equipment use. Leadership & People Management Lead, manage, and develop the Toolroom team, including Toolmakers, technicians, and apprentices. Manage team scheduling, time and attendance (TMS), holiday approval, overtime planning, and shift coverage. Conduct regular performance reviews, coaching, and development planning for the team. Assign daily tasks, set clear priorities, and ensure accountability for quality of work and timelines. Promote a strong culture of teamwork, ownership, and communication across the Toolroom. Job Specifications: The minimum education and experience required to perform this job competently. Qualified Time Served as Toolmaker. 3-5 years of people management experience is highly desirable. Min. of 3 years experience in an Injection Moulding Environment. Experience in a cGMP environment is desirable. Ability to work within a cross functional team. Good organizational, communication and computer skills. Application of Lean Problem-solving techniques. Ability to work on own initiative. High level of safe working practices and awareness. Skills: Toolmaker People Manager Moulding cGMP Problem Solving Benefits: Pension Healthcare