Social network you want to login/join with: Technical Operator - Team Lead, Castlebar Client: Baxter Location: Castlebar, Ireland Job Category: Other EU work permit required: Yes Job Reference: f96bf5b0292a Job Views: 6 Posted: 03.06.2025 Expiry Date: 18.07.2025 Job Description: Vantive: A New Company Built On Our Legacy Baxter is on a journey to separate our ~$5B Kidney Care segment into a standalone company. Vantive* will build on our nearly 70-year legacy in acute therapies and home and in-center dialysis to provide best-in-class care to the people we serve. We believe Vantive will not only build our leadership in the kidney care space, but also offer meaningful work to those who join us. *Completion of the proposed separation of Kidney Care from Baxter into a standalone company (to be named Vantive) remains subject to the satisfaction of customary conditions. Essential Duties and Responsibilities for our Lead Technical Operator: Set up the manufacturing process for the relevant product code according to batch instructions and router documentation. Perform routine quality checks, material changes, and take product samples as specified. Perform regular safety checks on machinery and equipment prior to production. Support process improvements using lean manufacturing and continuous improvement tools. Ensure team safety during shifts. Record detailed data using batch paperwork and interpret trend data. Maintain and review production documentation daily. Resolve manufacturing issues promptly; escalate issues as needed. Identify improvements proactively and see resolutions through to closure. Lead manufacturing tier boards and update visual management boards. Plan and execute training for team members on production processes. Manage sickness and holiday schedules as required. Adhere to company rules and work ethics. Ensure company brand materials and workspaces meet presentation standards. Perform shift handovers to ensure effective communication. Handle raw materials as per procedures. Follow safety procedures for material changes. Perform sanitisation procedures on equipment at scheduled times. The Person: Extensive knowledge of GMP and EHS regulations. Proficiency in Microsoft Office packages: Outlook, Word, Excel, PowerPoint. Experience working with automated systems. Leadership experience in a manufacturing or line environment is essential. Ability to lead a high-performing team. Ability to build and maintain excellent working relationships. Ability to work across multidisciplinary teams and at all levels. #J-18808-Ljbffr
Documentation Labeling Specialist, Castlebar Client: Baxter Location: Castlebar, Ireland Job Category: Other EU work permit required: Yes Job Reference: 3571552fdbda Job Views: 4 Posted: 03.06.2025 Expiry Date: 18.07.2025 Job Description: Vantive: A New Company Built On Our Legacy Baxter is on a journey to separate our ~$5B Kidney Care segment into a standalone company. Vantive* will build on our nearly 70-year legacy in acute therapies and home and in-center dialysis to provide best-in-class care to the people we serve. We believe Vantive will not only build our leadership in the kidney care space, but also offer meaningful work to those who join us. At Vantive, you will become part of a community of people who are focused, courageous, and don’t settle for mediocrity. Each of us is driven to help improve patients’ lives worldwide. Join us as we revolutionize kidney care and other vital organ support. *Completion of the proposed separation of Kidney Care from Baxter into a standalone company (to be named Vantive) remains subject to the satisfaction of customary conditions. Your role at Baxter: At Baxter, we are committed to ensuring a first-class candidate experience, and your role will be critical in enabling us to do this. This position has tremendous potential for growth. We’re searching for a Documentation/ Labelling Specialist to join our team based in Castlebar, Co. Mayo. As a member of our Quality team, you will be responsible for maintaining high standards of documentation and labelling management and implementing improvements across Castlebar and Swinford sites. You will play a key part in the quality and compliance procedures which are critical to saving and sustaining lives. You will collaborate with many departments and teams across both sites. Join us and our culture of great teams whose work values include speed, simplicity, courage, and collaboration. What are your responsibilities? Manage new/revised labelling in line with marketing and regulatory compliance, and complete all activities required for labelling updates. Print production labels as required. Follow procedures to maintain serialisation labelling requirements as applicable. Process and issue specification/procedure changes for the site as required. Coordinate archiving of documents. Update batch record parameters per procedures (Ebatch wrappers). Close validation protocols on Baxter Validation Database (VMS). Maintain current versions and labelling databases (Codesoft, Easi label, Ebatch/Prism). Route labelling and documentation on Baxter documentation system Teamcenter (TCU). Identify, develop, and implement best practices for the Label/Documentation Control Function to improve efficiency. Responsible for purchasing labelling and documentation items on Coupa. Perform other duties as assigned by business needs. What are we looking for? Graphic Art experience (not essential). Accountability, planning, prioritization, and deadline-driven work ethic. Strong computer skills – Microsoft Office and Adobe Acrobat. Familiarity with FDA regulations, GMPs, and SOPs. Experience with computerized proofreading systems, documentation, product lifecycle systems, serialization systems, digitized artwork storage, and documentation systems. Strong written and verbal communication skills. Attention to detail. Willingness to work flexible hours. #J-18808-Ljbffr
Vantive: A New Company Built On Our Legacy Baxter is on a journey to separate our ~$5B Kidney Care segment into a standalone company. Vantive* will build on our nearly 70-year legacy in acute therapies and home and in-center dialysis to provide best-in-class care to the people we serve. We believe Vantive will not only build our leadership in the kidney care space, but also offer meaningful work to those who join us. At Vantive, you will become part of a community of people who are focused, courageous, and don’t settle for mediocrity. Each of us is driven to help improve patients’ lives worldwide. Join us as we revolutionize kidney care and other vital organ support. *Completion of the proposed separation of Kidney Care from Baxter into a standalone company (to be named Vantive) remains subject to the satisfaction of customary conditions. PMO EMEA Sr Program Manager This position supports major programs in the Kidney Care Segment, including Project Evergreen, which involves driving integrated supply chain manufacturing network transfers, network capacity realignments, NPI, and major MIP programs. The role manages cross-functional resourcing from ISC, R&D, Regulatory, and Commercial organizations to deliver these programs. It involves identifying capital and operational budgets, including resources, required to successfully deliver the plan on time and within budget. The position requires the ability to gain support from key stakeholders and senior management. Essential Duties and Responsibilities: Lead cross-company, cross-segment, and cross-functional initiatives and teams with a broad scope: Identify, engage, and secure necessary resources and stakeholder commitment. Drive change by identifying barriers, making recommendations, and implementing solutions. Drive results by leading project teams, developing project plans, and executing according to established timelines. Communicate and present ongoing project status to senior management and stakeholders. Analyze complex data with an understanding of trade-offs between different business objectives. Present recommendations, gain commitment, and implement solutions. Partner with Network Planners to develop continuity of finished goods supply through product transition schedules. Qualifications: Project management qualifications and skills are required. Strong critical thinking skills, the ability to influence others, and effective communication skills are essential. Education and/or Experience: BS in Operations, Logistics, Engineering, or a similar degree is preferred; a minimum of 5 years of related project/program management experience is required. Benefits package includes Private Medical Insurance and an Annual Leave Package. #J-18808-Ljbffr
Social network you want to login/join with: Vantive: A New Company Built On Our Legacy Baxter is on a journey to separate our ~$5B Kidney Care segment into a standalone company. Vantive* will build on our nearly 70-year legacy in acute therapies and home and in-center dialysis to provide best-in-class care to the people we serve. We believe Vantive will not only build our leadership in the kidney care space, it will also offer meaningful work to those who join us. At Vantive, you will become part of a community of people who are focused, courageous and don’t settle for the mediocre. Each of us are driven to help improve patients’ lives worldwide. Join us as we revolutionize kidney care and other vital organ support. *Completion of the proposed separation of Kidney Care from Baxter into a standalone company (to be named Vantive) remains subject to the satisfaction of customary conditions. The Sr Manager, Fulfillment Services, serves as the KidneyCo relationship manager for its Baxter fulfillment related services, including ensuring that bi-directional services are provided per the agreement(s). Drives the closure of both short-term Manufacturing Services Agreements (MSAs) and Transition Services Agreements (TSAs) between the parties. The leader oversees any risk, discrepancies, and issue resolution between the parties. Essential Duties and Responsibilities Responsible for managing all aspects of the fulfillment services relationship for KidneyCo and Baxter. Acts as the relationship lead for KidneyCo for the region or distribution centers assigned. Strives to meet or exceed business needs relating to quality, delivery, and cost, including ensuring continuity of supply and cost management. Functions as a liaison between KidneyCo Quality Control, Quality Assurance, and Supply Chain, including Planning and Manufacturing. Supports and advises critical initiatives and contract negotiations that drive long-term relationship stability and success. Leads and supports business review meetings or other governance structures with Baxter to drive continuous improvement. Assists in developing metrics to analyze performance. Supports Finance in enabling and managing the invoice for products and services, including tracking and issue resolution. Drives closure of short term MSAs or TSAs and manages the associated discontinuation process and costs. Coordinates with Legal and Finance when an extension is required. Identifies and drives opportunities for efficiency and capacity improvements. Willing to travel, as the need arises. Able to maintain training status on KidneyCo specific work instructions and SOPs. Qualifications Demonstrated track record of effective leadership in a fulfillment or delivery setting, including issue resolution and building win-win solutions. Strong communication skills (oral, written, and interpersonal) and the ability to proactively identify and recommend solutions to problems. Ability to communicate problems in terms that are understandable to all levels of the organization, including C-Suite. Breadth of knowledge across pharmaceutical and medical device supply chain, Quality Systems, and regulatory requirements. Financial acumen, including cost management. Experience managing department Capital and Operating Expense budgets. Excellent organizational, communication, and time management skills needed to manage multiple ongoing projects simultaneously. Education and/or Experience Bachelor’s Degree or equivalent education and 7 years required. Experience in Pharmaceuticals and/or Medical Device supply chain is preferred. #J-18808-Ljbffr
Social network you want to login/join with: col-narrow-left Client: Baxter Location: Dublin, Ireland Job Category: Other - EU work permit required: Yes col-narrow-right Job Reference: 62441fdf68ac Job Views: 4 Posted: 02.06.2025 Expiry Date: 17.07.2025 col-wide Job Description: Vantive: A New Company Built On Our Legacy Baxter is on a journey to separate our ~$5B Kidney Care segment into a standalone company. Vantive* will build on our nearly 70-year legacy in acute therapies and home and in-center dialysis to provide best-in-class care to the people we serve. We believe Vantive will not only build our leadership in the kidney care space, it will also offer meaningful work to those who join us. At Vantive, you will become part of a community of people who are focused, courageous and don’t settle for the mediocre. Each of us are driven to help improve patients’ lives worldwide. Join us as we revolutionize kidney care and other vital organ support. *Completion of the proposed separation of Kidney Care from Baxter into a standalone company (to be named Vantive) remains subject to the satisfaction of customary conditions. Account Manager / Business Development Manager – Renal Care Division (Territory: Dublin and Northern Ireland) Reporting to the Head of Renal Care Ireland & Scotland, you will be responsible for the Baxter Chronic Renal portfolio including Peritoneal Dialysis, Home Haemodialysis and In- Centre Haemodialysis across Dublin and Northern Ireland. 80% of your time will be based in the Dublin Territory. Working in partnership with our NHS & HSE customers to impact improved outcomes for patients through change management and efficient patient pathways. This will be achieved by facilitating quality improvement programmes that will deliver true value. Presenting clinical, financial, and value-based solutions to key decision makers within the Healthcare sector. Elevate the role of Renal Home Therapies with our non-standard customers, targeting Divisional Directors and C-Suite customers. Develop, implement and review territory business plans that are aligned to a National strategy, as well as the ability to identify and act upon local opportunities. Portfolio sell to maximise growth opportunities and position appropriate clinical choice for our customers. Individual and group selling skills, as well as effectively navigating a variety of customer types through the sales cycle. Ability to negotiate consistent and transparent pricing to secure long term profitable and sustainable sales/market presence. Sales data and market analysis to inform activity and ensure a focused and results driven return on time. Contribute to the tender management process, including pre-tender focused activity, tender submission and post-tender follow up. Support the training of healthcare professionals on the safe, appropriate and effective use of Baxter Products to ensure optimum patient outcomes along with the Renal Therapy Specialist in the territory. Regular interaction with local and National team/peer group to continually drive a culture of collaboration, support and sharing best practice. Flexible mindset to thrive in a constantly changing external environment, as well as adapting to evolving internal business priorities. Effective use of CRM system to support planning, sequential selling and territory analysis. Work within the IPHA guidelines in the Republic of Ireland, and the ABPI guidelines in Northern Ireland. Education and/or Experience: D Degree or equivalent experience level qualification or relevant Clinical background. Able to demonstrate experience working in or around the Healthcare Sector. Successful sales background and/or able to demonstrate high level of knowledge aligned to relevant therapy area (desirable) Strong working knowledge of the HSE and NHS is critical including senior management and C Suite relationships (desirable). Who are you? You are a results driven and customer focused salesperson, with a systematic organised approach to work. You can work seamlessly within a multidisciplinary team and are generous in supporting others, but you are also very self-motivated to achieve your own goals. What are some of the benefits of working at Baxter? High importance placed on work life balance Commitment to growing and developing an inclusive and diverse workforce Baxter is committed to growing and developing an inclusive and diverse workforce – you can read more about our specific values here . #J-18808-Ljbffr
Social network you want to login/join with: Vantive: A New Company Built On Our Legacy Baxter is on a journey to separate our ~$5B Kidney Care segment into a standalone company. Vantive* will build on our nearly 70-year legacy in acute therapies and home and in-center dialysis to provide best-in-class care to the people we serve. We believe Vantive will not only build our leadership in the kidney care space, but also offer meaningful work to those who join us. At Vantive, you will become part of a community of people who are focused, courageous, and don’t settle for mediocrity. Each of us is driven to help improve patients’ lives worldwide. Join us as we revolutionize kidney care and other vital organ support. *Completion of the proposed separation of Kidney Care from Baxter into a standalone company (to be named Vantive) remains subject to the satisfaction of customary conditions. Reporting to the In Projects QA Manager, the Quality Engineer is responsible for providing technical guidance and support to project teams implementing process improvement, new product introductions, and other change programs in Castlebar & Swinford to ensure all activities are completed in compliance with Baxter and other GMP regulations. Key elements of the job include: Working within Validation/QA group on the preparation and execution of protocols for facility, equipment, new product introductions, software, and process validation. Act as an active team member on selected process & product improvement programs. Interpret and implement Baxter and GMP requirements associated with the process, change control, and validation requirements. Standardize systems, procedures, and practices relating to the implementation of technical requirements. Act as Quality Assurance approver of project plans and reports. Prepare and defend validation strategy to regulatory agencies. Ensure Baxter change control requirements are implemented. Provide technical advice to the project teams and obtain other technical input as required. Approve updated manufacturing and quality procedures. Confirm GMP compliance following project completion. Responsibility for ensuring that manufacturing operations are maintaining product quality standards. Ensure that corrective action is taken to prevent re-occurrence of problems. #J-18808-Ljbffr
