Consider joining Eurofins where people are the most important element in our business. Eurofins Biopharma Product Testing is a leading contract lab that provides testing and research services in the environmental, pharmaceutical, and biopharmaceutical sciences to clients worldwide. We have a fantastic opportunity for a Validation Engineer to join our Quality team in Dungarvan, Co Waterford. The purpose of this role is to execute the Metrology schedule and Metrology helpdesk activity required to support the Operations function, operating at the highest quality and productivity standards, ensuring agreed internal client requirements are entirely satisfied and that client expectations are met or exceeded. This person will be a key point of contact for all Metrology activities on a day-to-day basis, including external audits. Job Description Job Responsibilities Calibration and qualification of equipment as per formal schedule including completion and filing of documentation, labels and application of labels. Maintain the Metrology Helpdesk generating reports & metrics and completing own assignments. Calibration of equipment - unscheduled, following repair or movement. Completion of documentation, labels and application. Completion of Preventative Maintenance documentation, filing of service reports. Working of the Preventative Maintenance system i.e. documentation, issuing of log books, updating schedule according to changes, obtaining signatures, re-calibration where necessary. Servicing and repair: quotes and details, correspondence with vendors, organisation of vendor visits or despatching equipment where necessary, documentation following completion of repair and re-calibration. Maintenance of schedules: Calibration, Qualification, Preventative Maintenance. Putting new equipment into service as per ELL protocol for acquisition of new equipment. Checking and signing off external certificates of calibration and generating internal certificates for the same. Gathering information of external contractors, qualifications, procedures etc. and processing into the quality system. Organisation and maintenance of equipment files. Rolling review of calibration, maintenance and qualification SOPs. Assist the Computer Systems Validation team as required. Qualifications Education / Qualifications Primary degree or equivalent in related discipline (Life Sciences, engineering). At least 3 years’ validation experience in a laboratory or GMP regulated environment is desirable; preferably with calibration experience. Experience / Skills Previous experience in GMP regulated environment. Awareness of pharmaceutical processes for equipment calibration and validation. Ability to work independently or as part of a team. Excellent report writing, communication and organisational skills. Quality oriented with the ability to consistently work to industry and client standards. Experience with documenting analytical data and writing reports. Passionate about quality and customer service. Good communication skills both internally and externally. #J-18808-Ljbffr

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies. In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 50,000 staff across a network of more than 900 independent companies in over 50 countries and operating more than 800 laboratories. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing. In 2020, Eurofins generated total revenues of EUR € 5.4 billion, and has been among the best performing stocks in Europe over the past 20 years. Job Description Consider joining Eurofins where people are the most important element in our business. Eurofins is a leading contract lab providing testing and research services in the environmental, pharmaceutical, and biopharmaceutical sciences to clients worldwide. We have an opportunity for a Laboratory Assistant to work within our Molecular Cell Biology team. Duties will involve Logging samples on the laboratory computer system. Ensuring that daily consumables are monitored and stocked. Calibrating automatic pipettes and balances. Logging of columns and new equipment. Refilling desiccators and pipette washers when out of date. Ordering of all materials, including following up on ordered items. Preparing samples prior to analysis. Administration of documentation with reference to samples, i.e. filing. Qualifications NCEA certificate in a related discipline or administrative qualification is preferable. General Laboratory experience desired but not essential. GMP experience desirable but not necessary. Good team player. Good communication skills both internally and externally. Shift work may be a requirement. Flexible to work weekends if required. #J-18808-Ljbffr

Consider joining Eurofins where people are the most important element in our business. Eurofins Biopharma Product Testing is a leading contract lab that provides testing and research services in the environmental, pharmaceutical, and biopharmaceutical sciences to clients worldwide. What can Eurofins offer you? At Eurofins we offer careers not just jobs. Developmental opportunities and career progression. Private Medical Insurance when with the company for 2 years for all roles. Income protection and life assurance. Free parking onsite. Additional annual leave days with continued service. The opportunity to work on life-saving products. Work-life balance. Sports and Social events. We are currently recruiting for a full-time permanent Stores Assistant within our team in Dungarvan. The main aim of the role is to ensure that purchasing stock and store controls are handled in an efficient and cost-effective manner. Job Description Responsibilities include: Manage all stock movements and follow through any discrepancies that arise. Receipt stock in accordance with our policies and procedures. Approve all packing slips for payment once stock has been reconciled. Process claims where required on faulty goods, late deliveries, and short deliveries. Report to Manager on a daily basis any issues relating to goods movement. Organise outward packages via relevant couriers. Dispatch all outward goods using approved freight providers, processes, and in a timely manner. Responsible for ensuring purchasing documentation is completed accurately, in a timely manner and organized and filed correctly in accordance with company procedures. This person must ensure the stores are properly organized including labelling, FIFO, stacking, correct separation of goods, tidiness, etc. so items can be identified quickly and easily. Responsible for maintaining procedures to maintain effective, interdepartmental communication (e.g. with accounts, administration, chemistry, microbiology). This applies both to systems and feedback on the status of materials being purchased. Responsible for intake and labelling of all goods/supplies and for distribution to the stores or relevant areas in line with the company’s procedures. Responsible for maintaining a stock library of “one-off” chemicals and reference standards. To support stability activities when required. Working hours for the role are 39hrs per week, normally Mon-Fri but may include some weekend work. Qualifications Education Leaving Certificate or Equivalent. Experience Computer literate with good Microsoft Office skills. Required Licences Full Clean Valid Driving Licence mandatory. Skills and Abilities Ability to prioritise and organise work-load for the store room. Excellent organisational skills and good multi-tasker. Strong communication and interpersonal skills with the ability to interact with staff at all levels. Diligent, hard-working, takes ownership of tasks. #J-18808-Ljbffr

Company Description Consider joining Eurofins where people are the most important element in our business. Eurofins Biopharma Product Testing is a leading contract lab that provides testing and research services in the environmental, pharmaceutical, and biopharmaceutical sciences to clients worldwide. We have a fantastic opportunity for a Validation Engineer to join our Quality team in Dungarvan Co Waterford. The purpose of this role is to execute the Metrology schedule and Metrology helpdesk activity required to support the Operations function, operating at the highest quality and productivity standards, ensuring agreed internal client requirements are entirely satisfied and that client expectations are met or exceeded. This person will be a key point of contact for all Metrology activities on a day-to-day basis, including external audits. Job Description Job Responsibilities Calibration and qualification of equipment as per formal schedule including completion and filing of documentation, labels and application of labels. Maintain the Metrology Helpdesk generating reports & metrics and completing own assignments. Calibration of equipment - unscheduled, following repair or movement. Completion of documentation, labels and application. Completion of Preventative Maintenance documentation, filing of service reports. Working of the Preventative Maintenance system i.e. documentation, issuing of log books, updating schedule according to changes, obtaining signatures, re-calibration where necessary. Servicing and repair: quotes and details, correspondence with vendors, organisation of vendor visits or despatching equipment where necessary, documentation following completion of repair and re-calibration. Maintenance of schedules: Calibration, Qualification, Preventative Maintenance. Putting new equipment into service as per ELL protocol for acquisition of new equipment. Checking and signing off external certificates of calibration and generating internal certificates for same. Gathering information of external contractors, qualifications, procedures etc. and processing into the quality system. Organisation and maintenance of equipment files. Rolling review of calibration, maintenance and qualification SOPs. Assist the Computer Systems Validation team as required. Qualifications Education / Qualifications Primary degree or equivalent in related discipline (Life Sciences, engineering). At least 3 years’ validation experience in a laboratory or GMP regulated environment is desirable; preferably with calibration experience. Experience / Skills Previous experience in GMP regulated Environment. Awareness of pharmaceutical processes for equipment calibration and validation. Ability to work independently or as part of a team. Excellent report writing, communication and organisational skills. Quality oriented with the ability to consistently work to industry and client standards. Experience with documenting analytical data and writing reports. Passionate about quality and customer service. Good communication skills both internally and externally. Additional Information Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 47,000 staff across a network of more than 900 independent companies in over 50 countries and operating more than 800 laboratories. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2023, Eurofins generated total revenues of EUR €6.7 billion, and has been among the best performing stocks in Europe over the past 20 years. #J-18808-Ljbffr

Consider joining Eurofins where people are the most important element in our business. Eurofins Biopharma Product Testing is a leading contract lab that provides testing and research services in the environmental, pharmaceutical, and biopharmaceutical sciences to clients worldwide. What can Eurofins offer you? At Eurofins we offer careers not just jobs. Development al opportunities and career progression Private Medical Insurance when with the company for 2 years for all roles Income protection and life assurance Free parking onsite Additional annual leave days with continued service The opportunity to work on life saving products Work-life balance Sports and Social events Job Description We have a fantastic opportunity for a Scientist to join our Analytical Chemistry team in Dungarvan Co Waterford. The purpose of this role is to carry out scientific test procedures on client samples and produce accurate results within an acceptable time frame using company procedures and also to be responsible for completion of the more technically challenging analysis. This person will also work to develop any ancillary procedures associated with the methods and technical systems used; ensuring customer samples are completed within their required specifications. This role includes an expectation that provided appropriate training has been provided and a suitable level of technical competency and knowledge has been achieved, the Scientist will support complex analytical testing and high knowledge projects. This may be achieved by performing additional duties or functions (e.g. data review) that will be commensurate with your training and skillset. Job Responsibilities This person will carry out the non-routine tasks in the laboratory or carry out the particular type(s) of analysis assigned to them, back filling for analysts as required. Responsible for developing and validating new tests and procedures for company and clients. Responsible for the completion of specific technological projects and writing up the results of these projects accurately, confidentially and on time for the clients. Scientists are permitted to sign all technical documents once their training in this task is successfully completed. This includes laboratory reports, SOPs, protocols, investigation reports and any other documentation issued. Deputising for management as required. Responsible for updating any relevant documentation as required. Responsible for direct communication with clients in an appropriate manner. To liaise closely with the Section Manager to ensure that resources are available to guarantee that testing activities are completed to customer’s timelines. Responsible for the review of test methods for quotation purposes. Responsible for continually liaising with management, customers and other members of the organisation on any relevant problem areas or enhancements to the business. To identify any opportunities for improvement of quality and service and work with the team to implement continuous improvement. Qualifications Degree in a Scientific discipline 5+ years’ experience in a regulated GMP laboratory environment Analytical techniques (HPLC, LC-MS, GC, UV-Vis and Dissolution) Strong knowledge and experience with LC-MS is a requirement for this role Able to perform moderately complex and complex laboratory activities Good team player, organised, accurate, have strong documentation skills Passionate about quality and customer service. Good communication skills both internally and externally. Additional Information Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies. #J-18808-Ljbffr

Consider joining Eurofins where people are the most important element in our business. Eurofins Biopharma Product Testing is a leading contract lab that provides testing and research services in the environmental, pharmaceutical, and biopharmaceutical sciences to clients worldwide. We are currently recruiting for Bioanalytical Analysts for our Biopharmaceutical team within our Dungarvan facility. We are ideally seeking candidates with a minimum of 6 months GMP experience with a BSc/MSc qualification. The successful candidates must have exposure in Molecular ELISA and PCR. What can Eurofins offer you? At Eurofins we offer careers not just jobs. Development al opportunities and career progression Private Medical Insurance when with the company for 2 years for all roles Income protection and life assurance Free parking onsite Additional annual leave days with continued service The opportunity to work on life saving products Work-life balance Sports and Social events Job Description The main aim of the role is to carry out basic testing and to master the range of techniques appropriate for the work area. Become familiar with work practices and documentation requirements. Gain insight into the processes/procedures of the company’s business including customer awareness, lab safety and efficiency. Act on their own initiative and learn as quickly as possible any tests that they are required to do. Responsible for gaining proficiency in a certain number of tests/area of testing. Perform techniques/tests that they are qualified to do in terms of completed training records and as directed by the laboratory senior. Ensure that all documentation and calculations are carried out on time, accurately and legibly. Keep training records up to date and initiate training as per their training plan when free from work. Adhere to all company standards in the area of safety, housekeeping and quality, notifying management of any discrepancies. Ensure that customers’ requirements are fully met and be flexible to work in any area of the business as required. Identify opportunities for improvement of quality and service and work with the team to implement continuous improvement. Qualifications Minimum 6 months GMP experience with BSc/MSc qualification Exposure to Chromatography techniques, HPLC & UPLC Good team player, organised, accurate, with strong documentation skills Passionate about quality and customer service. Good communication skills Additional Information Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies. In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 61,000 staff across a network of more than 1000 independent companies in over 61 countries and operating more than 900 laboratories. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing. In 2022, Eurofins generated total revenues of EUR € 6.7 billion, and has been among the best performing stocks in Europe over the past 20 years. #J-18808-Ljbffr

Registered General Nurse required to join a progressive and dynamic nursing team in Caredoc. Location: Caredoc Treatment Centre, Dungarvan, Co Waterford Job Type: Part-time, flexible working hours with a weekend commitment. Applicants must possess: NMBI General Nurse Registration Computer literate Excellent communication and organisational skills Ability to work within a team environment Proven ability to work on one’s own initiative Please submit your CV to hr@caredoc.ie. The closing date for applications is [insert date]. Any informal queries can be emailed to hr@caredoc.ie or phone 059 9138199. #J-18808-Ljbffr

Consider joining Eurofins where people are the most important element in our business. Eurofins Biopharma Product Testing is a leading contract lab that provides testing and research services in the environmental, pharmaceutical, and biopharmaceutical sciences to clients worldwide. What can Eurofins offer you? At Eurofins we offer careers not just jobs. Developmental opportunities and career progression. Private Medical Insurance when with the company for 2 years for all roles. Income protection and life assurance. Free parking onsite. Additional annual leave days with continued service. The opportunity to work on life-saving products. Work-life balance. Sports and Social events. Job Description As a GMP Chemistry Testing Analyst, you will be responsible for conducting critical analytical tasks in our laboratory. Your primary responsibilities will include: Perform routine and non-routine analysis with precision and accuracy. Review and interpret analytical data with meticulous attention to detail. Prepare and approve test results in accordance with GMP standards. Meet customer requirements by delivering timely and accurate reports. Address customer queries professionally and provide significant results. Stay current with the latest technological advancements and method revisions. Train junior staff in analytical techniques and laboratory procedures. Revise Standard Operating Procedures (SOPs) as required. Participate in weekend and overtime work when necessary. Maintain thorough and accurate documentation. Provide laboratory coverage and support for colleagues as needed. Demonstrate flexibility to work in various areas of the business. Identify and suggest opportunities for improving quality and service. This role requires a commitment to maintaining the highest standards of analytical chemistry while ensuring customer satisfaction and regulatory compliance. Qualifications Minimum BSc in Science, preferably chemistry. Minimum 2 years’ experience in a GMP Environment, preferably in a QC role. Experience with finished product testing including HPLC, GC, UV-Vis, dissolution, etc. Experience with Waters and Empower III required. #J-18808-Ljbffr

Healthcare Assistant (HCA) Positions across Dungarvan - Take Control of Your Career Flexible Shifts Through Karo's Healthcare App Transform how you work with Karo - Ireland's innovative healthcare staffing app that puts YOU in control. How Karo Works: Download & Register on the Karo App Browse Available Shifts in Real-Time Choose Shifts That Suit You Get quick Confirmation Complete Your Shift Get Paid - Simple! Available Shifts From: Local Hospitals Nursing Homes Residential Care Centres Healthcare Facilities The Power is in Your Hands: ✓ Browse and book shifts directly through the app ✓ See exact pay rates before booking (Starting €14.98/hr) ✓ Choose locations that suit you ✓ Work as much or as little as you want ✓ No middleman or agency calls ✓ Instant shift confirmation ✓ Holiday pay included Perfect For HCAs Who Want: Complete schedule flexibility Direct access to multiple healthcare facilities The ability to choose their own pay rates Control over their work-life balance To pick up extra shifts when it suits them Required Qualifications: QQI Level 5 in Healthcare Support or equivalent Up-to-date Garda Vetting Relevant healthcare experience Ready to Take Control? Apply today! Join Karo - Where Healthcare Professionals Control Their Career! Job Types: Full-time, Part-time Pay: From €14.58 per hour Experience: Healthcare: 1 year (preferred) Licence/Certification: Level 5 in healthcare support (preferred) Driving Licence (preferred) Work Location: In person #J-18808-Ljbffr

New Restaurant, Iasc Bistro, in Dungarvan, Co. Waterford has exciting opportunities for new staff, including a Head Chef, Kitchen Porter, Waiters/Waitresses, and Bar Staff. Experience and excellent customer service skills are essential. Apply for Waiters/Waitresses & Bar Staff Name Email address Phone Number Add a cover note Attach a CV to your application Attach Supportive Documents Input is required. By clicking Send Application, I agree to allow JobsDoneDeal to share the information in this application. #J-18808-Ljbffr