About Abbott Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. Abbott in Ireland Abbott has been operating in Ireland since 1946 and serves the Irish market with a diverse range of healthcare products including diagnostics, diabetes care, medical devices and nutritional products. In Ireland, Abbott currently employs about 6,000 people across ten sites located in Dublin, Donegal, Clonmel, Cootehill, Galway, Kilkenny, Longford and Sligo. Abbott Diabetes Care Kilkenny Abbott Diabetes Care has opened a new site in Kilkenny, that is at the forefront of Diabetes care with the latest technology, to manufacture FreeStyle blood glucose test strips and FreeStyle Sensors for use in diabetes management. Among Abbott Diabetes Care leading brands are the FreeStyle Precision, FreeStyle Lite and FreeStyle Libre systems. This is how you can make a difference at Abbott: We currently have a requirement for a Lead Technologist to join our New Abbott Diabetes Care Kilkenny site. The following is required for this role: Please note we are building a talent pipeline for a Lead Technologist position due to start in late 2024. Key Responsibilities Plan, implement and lead complex Science and technical projects including product/process innovations supporting Sensor Manufacturing. Delivers high quality science and technology whilst ensuring compliance with respective regulatory and quality requirements. Ability to build relationships and manage technical activities, including aligning technology with manufacturing science and operations teams. Lead and participate in cross-functional problem-solving teams for troubleshooting, and complex scientific investigations. Seek opportunities for significant, process or product improvements/innovations. Act as a scientific expert, providing scientific support and knowledge. Applies specialized knowledge of product and process design. Present complex technical information to internal and external groups. Share scientific information and expertise. Experience in mentoring and teaching others to facilitate timely resolution of product and process technical issues. Recognize adverse trends and emerging issues. Propose and implement solutions to internal and external issues. Translates top-level goals to specific goals and aligns activities with respective strategic business priorities. Develop and maintain project timelines and provide updates and feedback to leadership. Lead with the evaluation and due diligence of external innovation opportunities. Education & Experience Minimum Level 7 qualification in a science related discipline. Experience and knowledge of Sensor Manufacturing is desirable. Minimum of 4 years’ people management experience in a technical capacity in medical device or pharmaceutical industry is desirable. Self-motivated and significant project experience with an ability to influence others are essential. Demonstrated ability to fully realize improvement initiatives. Demonstrated successes in a team environment, such as project teams, problem solving teams etc. Strong technical knowledge of design control process and experience of leading technology transfers. Advanced leadership skills in order to build an effective team by providing clear direction and defining priorities. Excellent communication / interpersonal skills. What We Offer Attractive compensation package that includes competitive pay, as well as benefits such as: Family health insurance, Excellent pension scheme, Life assurance, Career Development, Fantastic new facility, Growing business plus access to many more benefits. Connect with us at www.abbott.com and on LinkedIn, Facebook, Instagram, X and YouTube. Abbott is an equal opportunities employer. #J-18808-Ljbffr
About Abbott Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. Abbott in Ireland Abbott has been operating in Ireland since 1946 and serves the Irish market with a diverse range of healthcare products including diagnostics, diabetes care, medical devices and nutritional products. In Ireland, Abbott currently employs about 6,000 people across ten sites located in Dublin, Donegal, Clonmel, Cootehill, Galway, Kilkenny, Longford and Sligo. Abbott Diabetes Care Kilkenny Abbott Diabetes Care has opened a new site, in Kilkenny, that is at the forefront of Diabetes care with the latest technology, to manufacture FreeStyle blood glucose test strips and FreeStyle Sensors for use in diabetes management. Among Abbott Diabetes Care leading brands are the FreeStyle Precision, FreeStyle Lite and FreeStyle Libre systems. This is how you can make a difference at Abbott: Required We currently have a requirement for a Microbiologist to join our New Abbott Diabetes Care Kilkenny site. The following is required for this role: Responsible for developing and managing the site microbiology program. Responsible for maintaining the effectiveness of the site environmental monitoring program and product release testing in accordance with GLP, GMP and regulatory requirements. Ensuring CAPA activities are followed through to completion. Provide technical expertise to laboratory personnel and to the site. Provide leadership during problem solving situations related to microbial issues. Major Responsibilities Provide product and manufacturing microbial support in a cGMP regulatory environment. Develop and drive the site microbiology program, updating as appropriate. Manage and co-ordinate testing activities, including microbiological service providers and suppliers. Ensure that all work carried out is in compliance with the required regulatory standards, conforms to company policies and standard operating procedures (SOPs). Write documentation for test methods, cleanroom qualifications and equipment validation and provide guidance and feedback. Support laboratory set-up and maintenance of laboratory equipment and consumables. Drive the laboratory training program, knowing safety rules and regulations, and making sure all personnel are trained on safe work practices. Review laboratory test results, to ensure accuracy of data and timely communication of results. Perform environmental monitoring sampling of controlled cleanroom areas as required. Ensure cleanrooms are validated and controlled and comply with internal requirements, applicable regulations and ISO14644 class 8 standards. Provide technical guidance and support, in the areas of microbiological methods, cleanroom behaviours and cleanroom environmental monitoring. Support problem solving efforts related to microbial issues and provide technical advice as required. Support unplanned events and raise out of specification results in a timely manner. Initiate and complete CAPAs and Change Controls in accordance with site procedures. Analyse product quality and process data using statistical techniques to identify trends and implement improvement plans accordingly. Generate and present quarterly and annual reports. Liaise with key business stakeholders; QA, Manufacturing, Engineering, R&D, Regulatory Affairs and Purchasing to ensure timely completion of activities. Education & Experience Third level Science / Manufacturing or equivalent qualification. Minimum three years’ work experience in a Manufacturing / Science / Quality or equivalent environment. Connect with us at www.abbott.com and on LinkedIn, Facebook, Instagram, X and YouTube. #J-18808-Ljbffr
Abbott Quality Batch Reviewer in Donegal Town, Ireland About Abbott Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. Abbott in Ireland Abbott has been operating in Ireland since 1946 and serves the Irish market with a diverse range of healthcare products including diagnostics, diabetes care, medical devices and nutritional products. In Ireland, Abbott currently employs about 6,000 people across ten sites located in Dublin, Donegal, Clonmel, Cootehill, Galway, Kilkenny, Longford and Sligo. Abbott Ireland Diabetes Care Division Donegal The Abbott Diabetes Care division based in Donegal Town manufactures FreeStyle blood glucose test strips and FreeStyle Sensors for use in diabetes management. Among Abbott Diabetes Care leading brands are the FreeStyle Precision, FreeStyle Lite and FreeStyle Libre system. Primary Function: The Quality Batch Reviewer is mainly responsible for the product realization process (Review, approval and closure of in-process and Final lot release for both BGM and Libre sensor) in addition to supporting other departments to meet timelines and shipments thereby ensuring the site delivers safe and effective products whilst maintaining compliance with ADC policies and procedures. Responsibilities Include: Review and maintenance of BGM Device History Records. Review and approval of BGM final product inspection sheets for product release. Closure of Libre in-process & Final lots for product release. Responsible for working with Department Leads/Engineers to ensure any issues are addressed to progress the lots to final release (BGM & Libre). Performing tasks on computerised systems in order to release lots - SAP, POMs, Trackwise and Sharepoint. Supporting Technical and Operation Engineering to meet validation timelines in review of Validation Batch records. Responsible for the close out of MT (material transfer) forms on POMs. Tracking DHR review metrics to ensure site targets are met. Other tasks and duties as assigned. Education and Years Experience: Second Level Qualification. Minimum 2 years’ experience in Manufacturing environment. Proficient in the use of Microsoft Word, Excel & PowerPoint. Self-motivated, good attention to detail and works well under pressure. Previous knowledge of BGM/Libre production process is desirable. Accountability/Scope: Role reports to the Batch review Team Lead. Day Shift. An Equal Opportunity Employer. Abbott welcomes and encourages diversity in our workforce. We provide reasonable accommodation to qualified individuals with disabilities. To request accommodation, please call 224-667-4913 or email corpjat@abbott.com. #J-18808-Ljbffr
FIX TERM CONTRACT About Abbott Abbott is a global healthcare leader, we are committed to helping people live their best possible life through the power of health. For more than 135 years, we have brought new products and technologies to the world: in diagnostics, nutrition, cardiovascular, medical devices and branded generic pharmaceuticals -- that create more possibilities for more people at all stages of life. Today our 115,000 Abbott colleagues are working to help people live not just longer, but better, in the more than 160 countries we serve. Abbott in Ireland Abbott serves the Irish market with a diverse range of healthcare products, including diagnostics, medical devices, and nutritional products. In Ireland, Abbott employs over 6,000 people across ten sites. We have seven manufacturing facilities located in Clonmel, Cootehill, Donegal, Kilkenny, Longford, and Sligo and a third-party manufacturing management operation in Sligo. Abbott has commercial, support operations, and shared services in Dublin and Galway. We have been operating in Ireland since 1946. PURPOSE OF THE JOB The Training Specialist (Technology and Product) will be responsible for creating and delivering training on ARDx products, Complaint Handling processes and tools and other knowledge areas, as required, to the Technical Services teams and other ARDx personnel engaged in the complaint handling process. Including promoting efficiency and enhancing our customer experience by developing the skills of personnel. Responsibilities And Duties Identify individual and group training needs across the Technical Services network in conjunction with team leads/managers. Develop and maintain training offerings to ensure that necessary skillset is maintained within Technical Services teams. Deliver training on ARDx products and the underlying technology to facilitate effective troubleshooting. Deliver training on ARDx complaint handling processes to maximise customer satisfaction while maintaining regulatory compliance. Interface with Business Analyst and IT to prepare and deliver training on complaint handling applications. Monitor effectiveness of training on an ongoing basis and identify opportunities for continuous improvement. Scan the environment for new developments in technical customer service and evaluate suitability for inclusion in Technical Services training offerings. Establish and monitor the necessary training KPI’s to ensure that Technical Services group maintains compliance to Divisional trending metrics. Reviews and analyses data set trends with the technical service team leads/managers. Considering the data set trends provides direction in terms of setting training priorities and for process enhancement. Leads investigations of the negative trends and implementation of actions. Reviewing continuously opportunities to streamline processes and implement changes that will drive efficiencies and improve our quality compliance and customer’s experience. Provides support to TS team through real-time interventions: side-by-side, coaching sessions, feedback, and cascades. Responsible for the Induction and training of new team members ensuring that the highest levels of training are delivered and measured. Also maintain and grow personal knowledge and skills, technical and/or product knowledge within the team. Responsible for the record keeping of all TS induction programs and ongoing training as required. Writes procedures and other documentation needed for the compliant management of training preparation and delivery. Perform all job duties in accordance with relevant policies: Abbott policies & regulatory compliance. Partner with the QA/RA function to ensure adherence to the Quality Management System is at the core of all Technical service activities and meeting both ISO13485 and FDA 820 requirements on complaint management. Requirements Third level qualification in medical/science/engineering discipline. Training experience within the medical device industry and/or a clinical setting. Demonstrated success in managing training deployment using Multimodal Learning Strategies. Strong analytical skills, excellent attention to detail and good business judgment. Excellent interpersonal skills with an ability to achieve results through influencing others and maintaining strong links with other departments. Self-starter who possesses flexibility and ability to work under pressure in a fast-changing environment and ambiguous situations with shifting priorities. Effective communicator, both articulate & verbally presentable. Communicate technical knowledge to colleagues as necessary. Strong record of developing and implementing procedures within a compliance framework. Ability to effectively convey the subject matter to ensure comprehension to all audiences. #J-18808-Ljbffr
About Abbott Abbott is a global healthcare leader, we are committed to helping people live their best possible life through the power of health. For more than 135 years, we have brought new products and technologies to the world: in diagnostics, nutrition, cardiovascular, medical devices and branded generic pharmaceuticals -- that create more possibilities for more people at all stages of life. Today our 115,000 Abbott colleagues are working to help people live not just longer, but better, in the more than 160 countries we serve. Description The global Design Assurance team for IDEM, the Infectious Diseases Emerging Market Business Unit, supports R&D, Marketing, Clinical Operations, RA, QA and manufacturing functions based in Europe, Asia and US. The team is responsible for Design Control throughout the lifecycle of NPI projects, from ideation through to product launch including sustainment, for realization of our Lateral Flow Diagnostic Devices. The team supports a rapidly expanding business unit within Abbott. To ensure we can rapidly expand our Design Assurance capability, we are recruiting a Senior Design Assurance Engineer that will strengthen the team through implementation of best practice design controls and support the Organisation as a whole to maintain those within our projects. The Senior Design Assurance Engineer role will be instrumental in shaping the Design Control strategy to support our IDEM new product development pipeline. They will drive improvement in our processes, provide direction to and ensure compliance across all our supporting organisation – R&D, Marketing, QA, RA, Clinical Operations and Manufacturing. The specific role initially will be focused on a number of exciting new product development opportunities across our Manufacturing Plants, and partnering with our R&D teams to support the design control process to deliver the required design phase outputs. Responsibilities And Duties Design and development of packaging labelling and labelling solutions for New Product Introduction (NPI) and legacy products, including IFU’s. Participate in / lead cross-site, cross-function labelling related projects and activities. Generate project design assurance documentation and update label-related documentation as required. Communicate with various departments, functions and sites within Abbott on labelling related projects. Development of effective training collateral to ensure compliance to design control policies with the Core Teams, Extended teams and relevant functions within the Business Unit. Embed Design Assurance in all stages of the design concept and feasibility to support R&D through specification setting, test development and provision of statistical sampling to ensure robust prototypes and design at design freeze. Provision of on-going risk management, design control, quality systems and overall design assurance labelling expertise and leadership to the Project Core and Extended teams. Perform technical reviews of design documentation and labelling, attend at design reviews, coordinate and facilitate completion and update of design risk management documentation and acts as independent reviewer for all design activities including design changes. Design Control Support for audits including Abbott Corporate Audits and external Regulatory/ Governing Body audits (e.g. FDA/ WHO). Take the lead and front the team’s participation in audits. Ability to work in a matrix organisation where project deliverables are accountable to the Program/ Workstream Leader. Requirements Primary Degree level qualification in Science, Engineering or Technology, plus 7 years of Quality Engineering/ Design Assurance/ Regulatory Affairs work experience within a regulated environment (ISO13485/ FDA). Formal training in Medical Device Risk Management, Process Validation, Software Validation and problem Solving would be beneficial. Excellent data analysis skills. Proven ability to work well as part of a team and on own. Excellent communication skills to support virtual project requirements. Clear demonstrated experience in working in a diverse cultural environment. Excellent presentation skills to facilitate communication throughout the organisation. In addition, excellent use of virtual communication technology is required for effective workshop leadership and change management. Travel pending company policy, global and country regulations to Asia and Europe. #J-18808-Ljbffr
Location field must contain 'city, state' or a zip code to perform a radius search (e.g., Denver, CO or 46122 ). City and state must be separated by a comma followed by a space (e.g., Houston, TX ) Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. Abbott in Ireland Abbott has been operating in Ireland since 1946 and serves the Irish market with a diverse range of healthcare products including diagnostics, diabetes care, medical devices and nutritional products. In Ireland, Abbott currently employs about 6,000 people across ten sites located in Dublin, Donegal, Clonmel, Cootehill, Galway, Kilkenny, Longford and Sligo. Abbott Diabetes Care has opened a new site in Kilkenny that is at the forefront of Diabetes care with the latest technology, to manufacture FreeStyle blood glucose test strips and FreeStyle Sensors for use in diabetes management. Among Abbott Diabetes Care leading brands are the FreeStyle Precision, FreeStyle Lite and FreeStyle Libre systems. MAIN PURPOSE OF ROLE Specialist para-professional individual contributor with comprehensive knowledge in the area of Laboratory Technician. Ability to execute highly complex or specialized work. Knowledge acquired from several years of experience or specialist training in particular area. Works independently, applies standards yet adapts precedent and may make departures from established processes to resolve problems. May serve as a working team lead and/or supervise 1 or 2 lower level para-professionals. MAIN RESPONSIBILITIES As the Specialist para-professional in the Laboratory Technician Sub-Function, possesses advanced knowledge in performing a variety of technical procedures such as preparing routine solutions and reagents and performing routine reactions. Makes and records observations. Collects and prepares data for evaluation. Conducts laboratory support functions such as stocking and distributing supplies and equipment, arranging and dismantling apparatus, and collecting, washing, and storing glassware. Performs technical and record keeping duties in conformance with company and regulatory policies and standards to meet quality and accuracy requirements. May analyze compounds and manage corporate compound collection. Performs technical procedures in one or more of the following areas: Production, Research and Development, Quality Control/Assurance, and/or Compliance/Environmental. EDUCATION & EXPERIENCE Third level Science / Manufacturing or equivalent qualification. Preferred two years’ work experience in a Manufacturing / Science / Quality or equivalent environment. Electron beam or other sterilisation technologies experience desirable. Abbott is an equal opportunities employer. We provide reasonable accommodation to qualified individuals with disabilities. To request accommodation, please call 224-667-4913 or email corpjat@abbott.com. #J-18808-Ljbffr
FIXED TERM CONTRACT Abbott in Ireland Abbott serves the Irish market with a diverse range of healthcare products, including diagnostics, medical devices, and nutritional products. In Ireland, Abbott employs over 6,000 people across ten sites. We have seven manufacturing facilities located in Clonmel, Cootehill, Donegal, Kilkenny, Longford, and Sligo and a third-party manufacturing management operation in Sligo. Abbott has commercial, support operations, and shared services in Dublin and Galway. We have been operating in Ireland since 1946. Abbott Nutrition Our nutrition business develops science-based nutrition products for people of all ages, from helping babies and children grow, to keeping adult bodies strong and active. Millions of people around the world count on our leading brands – including Similac, PediaSure, Pedialyte, Ensure, Glucerna and ZonePerfect – to help get the nutrients they need to live their healthiest life. PURPOSE OF THE JOB As an individual contributor, with guidance from manager/team, functions to support Medical Safety & Surveillance (MSS) by reviewing, assessing, and summarizing medical device complaint information for complex investigations and risk assessments. Critically assess aggregate safety data from medical devices and communicates findings to internal stakeholders. Independently creates and delivers device medical safety training to a Global audience. Drafts documentation, including data reviews, clinical evaluations, literature reviews and standard operating procedures. Major Responsibilities Create and present medical safety related analyses, reports, and/or assessments orally and/or in writing within/ outside the Medical Safety and Surveillance department. Gather, critically analyze, and present findings from Medical Safety and Surveillance complaint data on a periodic basis, including tracking and trending activities. Ensure adherence to departmental standard operating procedures (SOPs), and draft new SOP as needed. Comfortable developing Medical Safety and Surveillance training materials and have strong presentation skills to provide training to a broad international audience. May write or assist in preparing, completing literature or website searches and data analysis for regulatory documentation supporting medical device registration. Conduct periodic literature searches, summarize findings and present information to a cross-functional team. Act as a backup to colleagues on day-to-day medical device complaints processing and conduct medical follow-up calls to customers as needed to obtain adverse event and/or complaint details. Determine complaint reportability to the competent authority as needed; drive on-time vigilance reporting within regulatory time-frames. Other duties/projects/support as assigned. EDUCATION & COMPETENCIES Bachelor of Science; a health science related background is a plus, such as dietitian, pharmacist, nurse, etc. RAC certification is a plus. 2-3 years Medical Device experience in activities such as aggregate data review, Risk Assessment, DFMEA review, and patient safety. Data analytics / strong Excel, PowerBI and/or data visualization skills. Medical knowledge to apply critical thinking and data analysis to Medical Safety data and/or Medical Device risk assessments. Basic understanding of Global Medical Device regulations (primarily EUMDR, MedDEV), clinical research, and international guidelines/standards related to medical devices (ISO, GSPR, MDGC, etc.). Willingness to learn other applicable Medical Device regulations, standards and guidelines. Drive to adhere to standard operating procedures (SOPs). Strong ability/experience in presenting medical and scientific training/data orally and in writing. Computer proficient (Windows, Word, Excel). Enjoys working in a collaborative environment and with a multidisciplinary, Global team. Works independently. Connect with us at www.abbott.com , on LinkedIn at www.linkedin.com/company/abbott- , on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews and @AbbottGlobal . #J-18808-Ljbffr
About Abbott Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. Abbott in Ireland Abbott has been operating in Ireland since 1946 and serves the Irish market with a diverse range of healthcare products including diagnostics, diabetes care, medical devices and nutritional products. In Ireland, Abbott currently employs about 6,000 people across ten sites located in Dublin, Donegal, Clonmel, Cootehill, Galway, Kilkenny, Longford and Sligo. Abbott Diabetes Care Kilkenny Abbott Diabetes Care has opened a new site, in Kilkenny, that is at the forefront of Diabetes care with the latest technology, to manufacture FreeStyle blood glucose test strips and FreeStyle Sensors for use in diabetes management. Among Abbott Diabetes Care leading brands are the FreeStyle Precision, FreeStyle Lite and FreeStyle Libre systems. This is how you can make a difference at Abbott: As a Cost Accountant you will be supervising a variety of accounting activities to ensure that the financial resources are managed in accordance with accounting principles and comply with all relevant regulations, laws, and standards. These activities may include financial analysis and reporting, general ledger maintenance, budgeting, and asset accounting. Responsibilities: Responsible for setting the standard cost for the product including costing over the long range plan (3-5 years) and presentation to Senior Management. Ensure month-end reporting is carried out efficiently and in line with agreed timetable. Assist Controller in Plan/LBE (latest best estimate/forecast) preparation including submission of Profit and Loss and Balance sheet and all related analysis v Prior year and Prior LBE to Senior Management. Provide business analyst support to manufacturing departments to assist in goal achievements and cost reduction projects. Set out standard work processes, visual management boards and other lean processes within finance. Carry out other assignments/projects as directed by the Controller. Management of fixed assets including but not limited to tracking, reporting, physical inventory and controlling. Develop a schedule for internal audits and oversee completion of same to ensure compliance with policies & procedures. Review RCEs (request for capital expenditure) and project expense and report on a monthly basis. Monitor as per budget. Ensure Environmental Health & Safety standards are met and all EHS regulations and procedures are adhered to. Demonstrate accountability and responsibility for EHS performance and compliance through active participation and support of Abbott’s EHS Program. Ensure to report any work-related injuries or illness to employee health and assist in the investigation. The job function will change where update procedures to GMP, EHS, Technical / New equipment, Quality procedures and SOP’s (standard operating procedures) are made. Active participation and support of Abbott’s EHS programs and attend EHS training as assigned. Ability to present to Executive Management. Strong written and verbal communication skills are essential. Good analytical and problem-solving skills required. Capacity to work alone to understand and summarise financial data into high quality, accurate and usable summaries. Strong computer skills, especially MS Office. SAP a distinct advantage. Education and Experience: Professional qualification in accountancy and/or degree in accounting. Excellent communication & interpersonal skills. 2 to 4 years' experience in the manufacturing industry. What we Offer Attractive compensation package that includes competitive pay, as well as benefits such as: Family health insurance, Excellent pension scheme, Life assurance, Career Development, Fantastic new facility, Growing business plus access to many more benefits. Abbott is an equal opportunities employer. For further information, and to apply, please visit our website via the “Apply” button below. #J-18808-Ljbffr
About Abbott Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. Abbott in Ireland Abbott has been operating in Ireland since 1946 and serves the Irish market with a diverse range of healthcare products including diagnostics, diabetes care, medical devices and nutritional products. In Ireland, Abbott currently employs about 6,000 people across ten sites located in Dublin, Donegal, Clonmel, Cootehill, Galway, Kilkenny, Longford and Sligo. Abbott Ireland Diabetes Care Division Donegal The Abbott Diabetes Care division based in Donegal Town manufactures FreeStyle blood glucose test strips and FreeStyle Sensors for use in diabetes management. Among Abbott Diabetes Care leading brands are the FreeStyle Precision, FreeStyle Lite and FreeStyle Libre system. Primary Function The Quality Batch reviewer is mainly responsible for the product realization process (Review, approval and closure of in-process and Final lot release for both BGM and Libre sensor) in addition to supporting other departments to meet timelines and shipments thereby ensuring the site delivers safe and effective products whilst maintaining compliance with ADC policies and procedures. Responsibilities Include Review and maintenance of BGM Device History Records. Review and approval of BGM final product inspection sheets for product release. Closure of Libre in-process & Final lots for product release. Responsible for working with Department Leads/Engineers to ensure any issues are addressed to progress the lots to final release (BGM & Libre). Performing tasks on computerised systems in order to release lots - SAP, POMs, Trackwise and Sharepoint. Supporting Technical and Operation Engineering to meet validation timelines in review of Validation Batch records. Generating DHR review forms for Libre complaint lots. Responsible for the close out of MT (material transfer) forms on POMs. Tracking DHR review metrics to ensure site targets are met. Other tasks and duties as assigned. Education And Years Experience Second Level Qualification. Minimum 2 years’ experience in Manufacturing environment. Proficient in the use of Microsoft Word, Excel & PowerPoint. Self-motivated, good attention to detail and works well under pressure. Previous knowledge of BGM/Libre production process is desirable. Accountability/Scope Role reports to the Batch review Team Lead. Day Shift. #J-18808-Ljbffr
About Abbott Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritional and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. Abbott in Ireland Abbott has been operating in Ireland since 1946 and serves the Irish market with a diverse range of healthcare products including diagnostics, diabetes care, medical devices and nutritional products. In Ireland, Abbott currently employs about 6,000 people across ten sites located in Dublin, Donegal, Clonmel, Cootehill, Galway, Kilkenny, Longford and Sligo. Abbott Diabetes Care Kilkenny Abbott Diabetes Care has opened a new site, in Kilkenny, that is at the forefront of Diabetes care with the latest technology, to manufacture FreeStyle blood glucose test strips and FreeStyle Sensors for use in diabetes management. Among Abbott Diabetes Care leading brands are the FreeStyle Precision, FreeStyle Lite and FreeStyle Libre systems. MAIN PURPOSE OF ROLE Perform quantitative and qualitative chemical or biological analyzes according to established scientific methods to ensure the quality of the organization's raw materials, in process products, and finished products. Main Responsibilities Plan, design, and conduct laboratory experiments to test the physical and/or chemical specifications of raw materials, in process products, and finished goods. Activities may include designing experiments; setting-up laboratory test equipment; calculating and analyzing test results; and preparing detailed reports with recommendations, applications, and conclusions. Evaluate the physical and/or chemical characteristics of raw materials and products such as permeability, disintegration, and crystal growth viscosity. Estimate the resources and time required to conduct an experiment and monitor performance to ensure these targets are met. Perform routine maintenance and safety checks on laboratory equipment to ensure it is in good working order. Education & Experience Third level Science / Manufacturing or equivalent qualification. Minimum four years’ work experience in a Manufacturing / Science / Quality or equivalent environment. Electron beam or other sterilisation technologies experience desirable. Knowledge in ISO 11137 desirable. Chemistry/Microbiology/Dosimetry Lab experience desirable. Abbott is an equal opportunities employer. #J-18808-Ljbffr
