Company Description 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 have a fantastic opportunity for a Team Leader to join our team in Dungarvan Co Waterford. The purpose of this job is to supervise members of a Biopharmaceutical chemistry team. This will include responsibilities such as planning work rotas, measuring productivity, training and development of staff, housekeeping, health & safety, quality, documentation, etc. to ensure the laboratory is run at maximum efficiency. Responsibilities Effectively manage all members of their team including areas such as work rotas, productivity, training & development, safety, quality, documentation, etc. to ensure the laboratory is run at maximum efficiency. Liaise closely with the Section Manager to ensure that resources are available to guarantee that testing activities are completed to customer’s timelines. Manage online reporting on LIMS, scheduling the work from start to sign off, developing and checking customer reports in a timely manner so as customer expectations are met consistently. Perform analysis as requested to ensure that customer’s deadlines are met. Review test methods for quotation purposes. Ensure that the Systems and Procedures are maintained to meet regulatory requirements. Provide continuous feedback to all members of their team on all items in relation to customer or organisational requirements/changes. Handle any customer related queries where necessary and liaise with their team to solve these queries if needed. Ensure all relevant documentation is authorised and filed accurately in line with company procedures. Communicate regularly with their team and all other ancillary groups to ensure information is transferred effectively throughout the organisation. Participate in routine regulatory and customer inspections. Ensure that all analysts are trained and have completed training records for all tests and other training completed. Ensure equipment is properly maintained and in the event of a breakdown that it is repaired in accordance with company procedures (with reference to timeliness, quality and cost). Keep their training records up to date and to initiate training where possible. Ensure that customers’ requirements are fully met and in so doing be flexible to work in any area of the business as is required. Identify any opportunities for improvement of quality and service and work with the team to implement continuous improvement. Qualifications Experience & Qualifications 5 years’ experience in a GMP analytical laboratory is desirable. At least 2 years’ supervisory experience is desirable. Ability to co-ordinate, schedule and prioritise analytical work. Excellent technical ability and strong, proven leadership skills. Passionate about quality and customer service. Good team player, organised, accurate, strong documentation skills. Good communication skills both internally and externally. Ability to understand customers’ requirements and to be able to devise and articulate the most appropriate solutions. #J-18808-Ljbffr
Consider joining Eurofins where people are the most important element in our business. Eurofins is a leading contract lab that provides testing and research services in the environmental, pharmaceutical, and biopharmaceutical sciences to clients worldwide. This position is to join our innovative Professional Scientific Services (PSS) programme as an employee of Eurofins. The programme places full-time analysts, technicians, scientists and technical support personnel managed by Eurofins directly at the client facility to provide long term staffing needs while maintaining the same services, expertise and cGMP compliance available at the Eurofins facility. This award-winning programme offers excellent career opportunities for people who have a proven track record in combining excellent technical ability with first class interpersonal and communication skills. Job Description We are currently seeking an Analytical Development Analyst to join our new and exciting PSS group in Limerick. This role will be responsible for day-to-day testing and support activities associated with method development and validation projects, including analytical transfer and validation according to regulatory guidelines and troubleshooting analytical issues obtained during method development. Experience / Skills Validate & verify analytical methods across a range of techniques including HPLC and Dissolution. Provide analytical testing across a range of techniques. Provide analytical support in technical transfer and troubleshooting. Demonstrate problem solving in delivering process and analytical understanding. Good understanding of requirements for working in a GMP environment. Ability to quickly learn new processes. Ability to communicate clearly and to form strong working relationships with colleagues. Ability to work on own initiative and be capable of developing solutions to problems. Good team player, organised, accurate, with strong documentation skills. Passionate about quality and customer service. Good communication skills both internally and externally. Qualifications A degree in Chemistry or a related discipline is required with a minimum of 2 years’ experience working in a GMP laboratory. Knowledge of method validation and HPLC testing experience is essential. Dissolution experience is an advantage. #J-18808-Ljbffr
Consider joining Eurofins where people are the most important element in our business. Eurofins is a leading contract lab that provides testing and research services in the environmental, pharmaceutical, and biopharmaceutical sciences to clients worldwide. We currently have exciting opportunities to join our innovative and multi award-winning Professional Scientific Services (PSS) teams. The excellent service provided via our PSS model is delivered while maintaining the same commitment to excellence, expertise and cGMP compliance available at our Eurofins facilities. We have an opportunity for a QC Support Laboratory Technician to join our Eurofins team based in our PSS site in Limerick. What can Eurofins PSS Limerick offer you? Developmental opportunities and career progression The opportunity to work with our client - a leading biotechnology company Location is easily accessible Private Medical Insurance Income protection and life assurance Annual discretionary bonus Free parking onsite Full use of the canteen facilities on the client site Additional annual leave days with continued service The opportunity to work on life saving products Job Description The purpose of this job is to provide laboratory support services related to sample shipment, controlled temperature / stability unit maintenance, stability sample coordination and reconciliation under the customer quality system, using customer company procedures, and while adhering to Eurofins general policies and standards. Job Responsibilities Support stability Coordinator and ensure that equipment operates in a compliant state; qualified, calibrated and properly maintained. Support QC Stability co-ordinator in the selection and ordering of CTU’s, stability chambers and related equipment. Maintain CTU inventory and monitor chamber performance. Coordinates sample shipments to outside contractors under the guidance of Sample Management, Stability and External Lab Coordinator. Collaborates with Sample Management and Stability/External Coordinators and other departments to receive material. Responsible for accurately logging samples into the relevant systems in a timely manner as required. Supports QC Stability Coordinator to prepare samples for inclusion in stability studies (aliquoting, labelling, distribution to appropriate stability chambers and also to remove samples from chambers according to protocol pull schedules and submits to appropriate testing group). Prepares labels for stability studies under the guidance of the Stability/External Coordinator. Responsible for ensuring all relevant documentation is completed accurately and logged where necessary. Coordinate sample disposal in conjunction with Sample Management and Stability Coordinator. Responsible for cleaning laboratory and equipment as required e.g. autoclaves, BSC’s etc. Dealing with customer queries and to contact designated personnel with any relevant information or issues with service in general. Assisting in laboratory investigations as appropriate. Assisting laboratory analytical personnel and perform ad-hoc lab duties as required. Qualifications Degree in relevant scientific discipline. Minimum of 6 months laboratory/GMP experience. Good planning and organisational skills. Accuracy and attention to detail. Good team player. Good communication skills both internally and externally. Familiarity with pharmaceutical and/or laboratory operations (GMP, Documentation, Autoclaves, Sample Management). Note: Shift work is required for this role. Working hours 7am to 7pm. The working week is as follows and these rotate week on week. #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
Business Development Manager | Eurofins | Ireland Company Description 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 laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate. Job Description We’re looking for a Business Development Manager whose primary focus will be to retain and grow a regional portfolio of allocated accounts and to sell the company’s services and products to ensure the achievement of targets, Key Performance Indicators (KPI’s) and overall business objectives. What will you be responsible for? Generating prospects, attending sales meetings, developing quotations and converting quotes into new business; Undertaking price reviews and renegotiation of commercial agreements; Delivering forecasted growth of sales within your allocated accounts; Creating a strategy document for Key Accounts; Preparing reports; Ensuring that the Customer Relationship Management (CRM) system is maintained with up-to-date information; Maintaining an effective and dynamic knowledge base of competitors’ activities within CRM. Qualifications Are you our kind of extraordinary? Education: Bachelor’s degree in Business, Marketing, Engineering, Environmental Science, or a related field; MBA is a plus; 8+ years of experience in business development, sales, or marketing in the sustainability industry; Industry-specific knowledge in environmental testing would be desirable. Additional Information What can we offer you? Permanent employment; Flexible working hours; A dynamic team with flat hierarchies and opportunities for active participation; Personal and professional development opportunities, as well as exclusive benefits for Eurofins employees; Working from home. We support your development! Do you feel you don’t match 100% of the requirements? Don’t hesitate to apply anyway! Eurofins companies are committed to supporting your career development. We embrace diversity! The Eurofins network of companies believes in strength and innovation through diversity, being an Equal Opportunity Employer. We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique. Sustainability matters to us! We are well on our way to achieving our objective of carbon neutrality by 2025, through a combination of emission reduction and compensation initiatives. We encourage our laboratory leaders to make sustainable changes at their local level, and in addition to their initiatives we also count on our dedicated carbon reduction team to help us to achieve this goal! Find out more on our career page: https://careers.eurofins.com/ #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. 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 qualification. Exposure to ELISA and PCR. Good team player, organized, accurate, and have strong documentation skills. Passionate about quality and customer service. #J-18808-Ljbffr
