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 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 applicants with experience but will also consider Graduate applications. Ideally, the successful candidates must have exposure in a mixture of techniques. 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 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/areas 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 where possible 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 any opportunities for improvement of quality and service and work with the team to implement continuous improvement. Qualifications Experienced and graduate applications accepted with BSc/MSc qualification. Exposure to Chromatography techniques, HPLC & UPLC, GC, CE, ICE, LCMS. Large Molecule Testing. Good team player, organized, accurate, with strong documentation skills. Passionate about quality and customer service. Good communication skills. #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 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 dispatching 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
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 Molecular 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/PhD 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. 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 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. Be 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 their training records up to date and initiate training as per their training plan where possible 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/PhD qualification. Exposure to Molecular Techniques, ELISA & PCR. Good team player, organized, accurate, and have strong documentation skills. Passionate about quality and customer service. Good communication skills. #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 Molecular 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/PhD 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. 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 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 their training records up to date and initiate training as per their training plan where possible 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/PhD qualification. Exposure to Molecular Techniques, ELISA & PCR. Good team player, organised, accurate, and have strong documentation skills. Passionate about quality and customer service. Good communication skills. Seniority level Mid-Senior level Employment type Full-time Job function Science #J-18808-Ljbffr
Eurofins Scientific is an international life sciences company, which provides a unique range of analytical testing services to clients across multiple industries. The Group believes it is the world leader in food, environment, 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 for supporting clinical studies. In addition, Eurofins is one of the leading global emerging players in specialty clinical diagnostic testing. In 2020, Eurofins generated 5.4 billion Euro proforma turnover in 800 laboratories across 50 countries, employing about 50.000 staff. Job Description We are actively recruiting for an Operational Excellence Specialist to join our team in Dungarvan. The purpose of this role is to support the drive the successful implementation of “Eurofins BPT OPEX / Lean / Six Sigma Methodology” in the laboratories and across the site. Responsibilities Coordinate assigned Continuous Improvement projects Analyse and improve Operational & Business processes SME for Lean & Six Sigma methods & successful application Implement project plans, and monitor progress against plan Teach and drive Lean / Six Sigma tools and techniques to local employees, contributing & enabling a culture of continuous improvement Maintain and build KPI’s and ensure all Lean / Six Sigma project targets and timelines are managed, ensure there is clear and adequate ownership and responsibility Support and enable a CI culture within the organisation through “lead by example” Contribute to and document best practice Deputise for Site OPEX Lead Clear communicator to cross functional stakeholders Support site sustainability plan What are we looking for? Scientific or Engineering third level qualification essential Lean / Six Sigma Green Belt certification minimum essential, Black Belt certification is desirable Previous experience working in a similar role Project Management desirable Hard working self-motivated and professional team player Ability to work well under pressure Ability to multi-task, prioritize, organise and co-ordinate your own workload Ability to work to deadlines Demonstrated teamwork skills Ability to learn new tasks What are we offering? Competitive salary Bonus Health Insurance Pension Sick Leave Paid Maternity Leave, Parental Leave, Paternity Leave Income protection Life Assurance Sports & Social club #J-18808-Ljbffr
Job Description Eurofins BPT are actively seeking a Senior Quality Specialist to join our Quality team in Dungarvan, Co Waterford. The purpose of this job is to support the implementation and development of the Quality System in the company. Continuous improvement of Quality Management System, including but not limited to internal audits, supplier management, change control, exception systems. Prepare agenda for weekly Quality Meetings, to include metrics on number of documents pending review etc. Deputise for the Quality Manager, as requested in terms of review and approval of documentation and supervision of staff as necessary. Responsible for ensuring all internal and supplier audits are completed as scheduled. Management of Controlled Drugs. Operation and maintenance of the Exceptions system. Co-ordinating the resolution of issues surrounding non-conforming work as necessary with Laboratory Management. Completion of internal audits. Operation and maintenance of the Audits module within LIMS. Support the co-ordination and compilation of client audit and regulatory inspection responses. Support the co-ordination and compilation of information for regulatory bodies as requested. Support the hosting of client audits and regulatory inspections – point of audit set up, Quality Department representative during audits. Proposing and implementing improvements to the quality system in line with industry best practices and standards. General upkeep of the quality system through a plan of continuous improvement from CAPAs, audits, review of procedures and regulatory/legislation updates. Review and Co-ordination of technical and quality agreements. Co-ordinating and submitting information to clients as requested – questionnaires, requests for regulatory information. Operation of the Supplier Approval system. Administration and control of external documentation including client methods and SMIS. Delivery of quality systems training as required. Assist in the preparation and delivery of the Annual Management Review process. QA approval of procedures and protocols. QA approval of certificates of analysis and technical reports. QA approval of Exceptions. Controlled Drugs: Responsible for the activities related to controlled drugs system across site. Obtaining / maintaining licences for possession or import or export of controlled drugs as necessary. Point of contact for the HPRA in relation to the activities involving controlled drugs management on site which includes but not limited to reconciliation, stock returns, maintenance of licences, adherence to procedures and compliance to the legislations. Qualifications Education / Qualifications Bachelors degree in a scientific discipline Quality, Science, engineering or other relevant scientific or technical discipline. 5 years’ experience in a laboratory in GMP regulated environment, with at least 2 years of QA role experience is desirable. Working knowledge of pharmaceutical quality systems. 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. Positive and tenacious approach to work. Highly organised, methodical and systematic approach to work. Passionate about quality and customer service. Good communication skills both internally and externally. Ability to understand clients’ requirements and to be able to devise and articulate the most appropriate solutions. 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
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 We currently have opportunities for Analysts to join our Raw Materials Chemistry team in Dungarvan Co. Waterford. The purpose of this job is to carry out scientific test procedures on customers’ samples and produce accurate results within an acceptable time frame using company procedures. Job Responsibilities To perform routine and non-routine analysis, as requested by the laboratory. To carry out data review. To prepare and approve results for tests in which they are deemed competent. To be aware of customers' requirements and should strive to meet those requirements keeping in mind the cycle is not complete until the customer has obtained their report. To deal with customer queries and telephone significant results to customers. To keep up to date with any technological or method revisions in their area, ensuring their training is complete and adjusting their work as required. To train other more junior members of staff in analytical techniques as required. To revise SOPs as required by the laboratory. To participate in the company’s weekend rota and/or overtime schedule, as required. To be responsible for updating any relevant documentation when requested. To provide cover for other members of staff as required. To ensure that customers’ requirements are fully met and in so doing be flexible to work in any area of the business as is required. To identify any opportunities for improvement of quality and service and work with the team to implement continuous improvement. Qualifications Minimum BSc in Science, preferably chemistry. Minimum 2 years’ experience in a GMP Environment, preferably in a QC role. Experience with Raw Material testing including FT-IR, KF, HPLC, GC, UV-Vis etc. Experience with Waters and Empower III an advantage. #J-18808-Ljbffr
Eurofins are currently seeking Cleaning Operatives on our site in Dungarvan. The main responsibilities of this role are to ensure the premises, building and laboratory glassware are kept clean and tidy at all times, keeping in mind efficiency, quality and accuracy standards as required by the company. Full-time and part-time options are available with a variety of working hours available. Job Description Job Responsibilities Cleaning and maintaining the building at an acceptable housekeeping level in accordance with company procedures. Disposing of waste in the skip in the most efficient and space-efficient manner, i.e., collapsing boxes prior to placing them in the skip. Stripping and re-sealing the floors when required. Sanitisation of pharm micro labs and completing log books. Responsible for washing all glassware as per the appropriate company procedures. Responsible for general cleaning around the building, i.e., general dirt problems, toilets, outside, etc. (Providing housekeeping cover during the day in the absence of evening staff.) Working as part of a team, this person will be responsible for providing cover for other members of staff as required. Responsible for ensuring all canteen areas are kept clean and tidy at all times. Qualifications Experience in industrial cleaning GMP environment is preferable but not essential. Good team player. Good communication skills both internally and externally. #J-18808-Ljbffr
About the Company 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 pharmaceutical and biopharmaceutical sciences to clients worldwide. What can Eurofins offer you as an employee? At Eurofins we offer careers not just jobs. Developm ental 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. About the Role As a Quality Control 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 Responsibilities 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
