By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description: Job Purpose To assist in daily and monthly activities supporting continued product supply to Market. Shipping documentation, Documentation release to Production and Contract Manufacturers, and confirming material availability will be critical elements of this role. Work with the Supply and Finance departments on the preparation of monthly reports. This role will give the candidate a broad overview of manufacturing and distribution operations and the critical interdepartmental responsibilities and communication to deliver business performance (Supply Chain, Operations, and Customers). Responsibilities Liaise with Finance and Supply Chain on the following: Monthly CMO reconciliations – investigate variances against actuals. Prepare Monthly Inventory Provision Report for CMO. Processing of inventory write off requests for both CMO and TIL Bray Plant. Work with Finance to ensure the correct cross charging of Sample Orders to customers. Work with the Finance shared service group to resolve transfer pricing / invoicing issues. Master Data Updating master data in SAP. System housekeeping in line with monthly Supply Chain cycle. Gathering of Master Data as required by Strategic Business Projects. Support of Planning Function Requirement to utilize both SAP and local System to issue work orders for production. Material Requisitions for Warehouse and follow up on Material availability. Creation of shipping document ‘packs’ required for each shipment. Support of Supply Chain Function Action Requests for Initial Commercial Supply or New product launches. Review and processing of open orders for Contract Manufacturers. Processing of Open Orders for Takeda Japan. Processing of Open Orders for Alogliptin Products. Monthly KPI Reporting Preparation of monthly KPI reports for Supply Chain and Planning to include: Production Plan Conformance. Performance against budgeted volume. Inventory Reporting DOH Analysis. Other Responsibilities Participate fully in any cross functional training initiatives. Drive and promote the corporate values of Takeda-ism within the workplace. Other duties as required and directed by the Director; HR or other Officer appointed by the Board of Directors. Educational Requirements Leaving Certificate or equivalent. Currently studying towards a 3rd level degree in Business, Supply Chain, Accounting or other relevant disciplines. Relevant Experience/Criteria Advanced Excel skills. SAP experience would be an advantage but not a requirement. Locations: Bray, Ireland Worker Type: Employee Worker Sub-Type: Paid Intern (Fixed Term) (Trainee) Time Type: Full time #J-18808-Ljbffr

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description: People First: At Takeda we are dedicated to improving the health and well-being of all people and bringing them the hope of a brighter future. It is our passion that transforms every job into meaningful action. Our people are the heart of Takeda. For Takeda Ireland Ltd, we are looking for a Quality Control Analyst for a full-time fixed-term (11-month) position at our location in Bray, Co. Wicklow, Ireland. As a QC Analyst, you will play a pivotal role in ensuring the highest standards of quality and compliance in our pharmaceutical products. This position requires a deep understanding of Good Manufacturing Practice (GMP) and current FDA & EMEA regulations for solid oral dosage pharmaceuticals. Your expertise in manufacturing, packaging, and validation processes will be crucial in maintaining our commitment to excellence. You will have the opportunity to apply your analytical and technical skills in a dynamic and supportive environment, contributing to the development of life-saving medications. Your dedication to quality will help us uphold our reputation for delivering safe and effective products to patients worldwide. Your tasks in detail: Ensure strict adherence to GLP/cGMP standards. Conduct comprehensive testing of laboratory samples. Perform laboratory tests following written procedures or pharmacopoeia guidelines. Accurately record and report analytical results. Operate, maintain, and calibrate laboratory instruments. Develop and execute validation protocols for instruments and methods. Maintain detailed and up-to-date training records. Keep the laboratory environment clean, organized, and safe. Manage the ordering, receiving, and control of laboratory chemicals, reagents, and consumables. Promote and embody the corporate values of Takeda-ism and foster a culture of safety awareness. Your profile: A minimum of a BSc. in science or a related discipline, providing a strong foundation in scientific principles and methodologies. Proven experience in the pharmaceutical industry, showcasing your ability to navigate and excel in a highly regulated environment. At least 2-3 years of hands-on experience in an analytical lab, demonstrating your proficiency in laboratory techniques and procedures. Excellent organizational, communication, interpersonal, and report writing skills, enabling you to effectively manage tasks and collaborate with team members. Adaptability to changing priorities, ensuring you can thrive in a dynamic and fast-paced work environment. Opportunity to work in a cutting-edge pharmaceutical company, contributing to the development of life-saving medications. Engage in continuous learning and professional development, enhancing your skills and advancing your career. What you can look forward to with us: Competitive Salary Including performance-based bonuses. Retirement Plan Employer contributions to your retirement plan. Comprehensive Insurance Employer-funded private medical insurance with dependants’ cover, life insurance, and flexible options like dental insurance, partner life insurance, and serious illness protection. Electric Charging Points Available at parking locations. Employee Assistance Program Support for personal and professional challenges. Wellbeing and Engagement Dedicated teams to support your wellbeing. Family-Friendly Policies Supportive policies for a balanced work-life. Generous Vacation 26 vacation days plus additional days for service milestones and humanitarian volunteering leave. Development Opportunities Coaching, mentoring, educational programs, and formal training. Subsidized Canteen Enjoy meals at a reduced cost. Flexible Benefits Options like fuel card, bike to work, commuter ticket, and insurance deals. More about us: At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work. Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world. Empowering our people to shine: Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, or any other characteristic protected by law. If you are interested in this opportunity, we look forward to receiving your application via our online tool! Locations: Bray, Ireland Worker Type: Employee Worker Sub-Type: Fixed Term (Fixed Term) Time Type: Full time #J-18808-Ljbffr

Main purpose of the role: Ensure the Bakery Department operates efficiently and effectively at all times and provides our customers with excellent quality products and services. The ideal candidate will have/be: HACCP training is desirable but not necessary Previous customer service experience is an advantage The ability to work as part of a team in a fast-paced environment, ability to multi-task under pressure A passion for food and the ability to inspire shoppers Main duties: Actively live SuperValu brand-values i.e. Genuine, Passion for Food, Vibrant, Committed, Innovative and Imaginative Prepare customers' bakery orders Bake, prepare and display the Bakery Products sold throughout the day Ensure that the counter displays across all fresh food departments are to the highest standards at all times throughout the day Demonstrate your passion for quality food by sharing knowledge, recipes and personal recommendations with customers Deal with all customer queries efficiently, professionally and in line with store policy #J-18808-Ljbffr

O’Neill & Flanagan Auctioneers requires an individual to apply for an exciting opportunity to join our successful and expanding team. We specialize in providing top-tier property sales across Wicklow Town and surrounding areas. Due to continued growth, we're looking to add passionate and motivated professionals to our team. Requirements: Holder of PSRA Licence preferably categories A, B, and C. Minimum of 2 years’ experience in the residential property market with an up-to-date PSRA Licence. Local knowledge would be of benefit. Full clean driving license with own car. Confident outgoing personality with strong ability to engage with various participants in the marketplace from vendors, buyers, investors, and institutions. Strong IT skills and familiarity with relevant property software packages (Microsoft). Capable of working on own initiative in addition to working in a team environment. Proven ability in negotiating and selling skills. Competitive salary offered, based on experience and suitability for the role. If you believe you meet the above criteria and are ready to take the next step in your career, we would love to hear from you. Please reply in writing at your earliest convenience to info@oneillflanagan.com . Rest assured, all applications will be treated with the utmost discretion. #J-18808-Ljbffr

Social network you want to login/join with: Territory Sales Manager - Cardio/Endovascular Equipment - Republic of Ireland For over half a century, our client has had a mission to invent better ways to serve clinicians and their collaborators. As a global leader in breakthrough cardiovascular and endovascular solutions, they are the people behind the people who keep saving lives, dedicated to being the heart of innovation to transform cardiovascular care. They are currently looking for an experienced Territory Sales Manager who will be fully responsible for the territory described, promoting and selling the complete range of cardiovascular and endovascular solutions, ensuring an on-target performance within the projected budget for the territory. Responsibilities include: Manage a portfolio of new and existing accounts to achieve long-term success Lead territory KOL strategy, fostering positive long-term relationships and ongoing engagement with strategic customers Identify opportunities to generate new business using existing and potential customer networks Play an active role within the team by providing market and competitor intelligence, feedback on local trends and working towards agreed objectives Be the clinical expert and product champion across the portfolio, ensuring proficient knowledge of all products They are looking for a highly talented individual with a passion for sales, fostering customer relationships and identifying innovative ways to add value for the clinical and non-clinical customers. The position represents an excellent opportunity for a motivated and enthusiastic individual who wishes to develop within a company that is planning an exciting future with a rich product pipeline. Qualifications & experience required: Account Management / Sales experience within the medical device industry Experience in the cardiovascular/endovascular space is preferred Ability to learn and understand complex clinical product knowledge and clinical data Must be self-motivated to drive ideas and develop business opportunities Ability to identify business opportunities and the ability to persuade and influence others. Ability to work independently with a high competency in time management Able to build and maintain strong business and customer relationships Ability to problem solve and develop a customer-centric mindset A thorough understanding of procurement channels and purchasing structures A Highly Competitive Basic, Bonus and Benefits Package will be offered. Please apply online or call CHASE on 0131 553 6644 for further information. #J-18808-Ljbffr

Regulatory Specialist - Transfers 12 mth FTC We are Oriflame corporate.oriflame.com The role is a temporary role to support the regulatory function on all tasks related to the transfer of cosmetic products from the manufacturing site in Poland to other manufacturing sites in Europe. It will require assessment on the impact to markets and supporting the markets in ensuring successful registrations of the portfolio. Key Responsibilities Conduct assessment of impact of transfers to global portfolio and highlight risks to manager. Supporting the review and approval of updated artworks. Represent regulatory team in transfer project meetings. Liaise with suppliers to obtain necessary documents to support re-registration of products globally. Support the registration team in preparation, compilation & dispatch of all required regulatory information for transferred products. Notification of transfer products on EU & UK CPNP portal as required. Ensure regulatory database is updated and maintained for relevant products. Ad hoc support to Regulatory Team & Manager if required. Qualifications Science related degree. Experience in regulatory affairs. Previous experience in the beauty industry is desirable. Experience in managing multiple projects and tasks. What do we offer? Hybrid working, flexible working hours, 23 days holiday p.a., discount on Oriflame products. Seniority level Entry level Employment type Temporary Job function Legal Industries Personal Care Product Manufacturing Does this match your profile and expectations? Then don’t hesitate and apply now. Or spread the word to people who might be the right match. #J-18808-Ljbffr

O’Neill & Flanagan Auctioneers requires an individual to apply for an exciting opportunity to join our successful and expanding team. We specialize in providing top-tier property sales across Wicklow Town and surrounding areas. Due to continued growth, we're looking to add passionate and motivated professionals to our team. Experience in New Home sales is essential. Requirements: Holder of PSR Licence preferably categories A, B, and C. Full clean driving license with own car. Membership of a recognised professional body is preferable – IPAV/SCSI. Proven track record in handling property sales from initial engagement to fully concluding the sales process. Confident, outgoing personality with strong ability to engage with various marketplace participants from vendors, buyers, investors, and institutions. Strong IT skills and familiarity with relevant property software packages (Microsoft). Capable of working on own initiative in addition to working in a team environment. Proven ability in negotiating and selling skills. Competitive salary offered, based on experience and suitability for the role. If you believe you meet the above criteria and are ready to take the next step in your career, we would love to hear from you. Please reply in writing at your earliest convenience to info@oneillflanagan.com . Rest assured, all applications will be treated with the utmost discretion. #J-18808-Ljbffr

Social network you want to login/join with: Sales Account Manager - Medical Devices - B2B, Bray Location: Bray, Ireland Job Category: Other EU work permit required: Yes Job Reference: 14d9aa659f6f Job Views: 3 Posted: 18.03.2025 Expiry Date: 02.05.2025 Job Description: On behalf of our client, a growing global medical devices company, we are recruiting for a Sales Account Manager for B2B. This role will look after the European market. The role will be hybrid, with approx 2/3 days a week in South Dublin office. Responsibilities Managing and developing distributors and MTO customers in European markets, ensuring client satisfaction, achieving sales targets, and engaging in key account management activities such as weekly calls and monthly reviews. Implementing sales plans to drive revenue growth and meet or exceed sales goals. Leading and moving the opportunities along, negotiating and finalising deals, and working with internal parties to assist the customer with the Tendering Process. Tracking and reporting on account activity and providing monthly status updates to management. Advising customers on our products, performing demos independently and devising solutions for them. Providing feedback from clients and users to the Product Development, Marketing, and Supply Chain teams to continuously improve customer satisfaction. Conducting bi-weekly market research to identify new opportunities and competitors' strengths and weaknesses. Suggesting improvements to stay competitive. Participating in conferences, industry events, and professional development activities to expand the network and enhance knowledge. Coordinating with the Marketing team to develop and implement strategies to promote our products and services. Understanding and staying up-to-date with the latest medical research to facilitate informed discussions with clients and exploring the Middle East Markets for new opportunities. Qualifications Bachelor's degree in Business, Marketing, or a related field. Minimum of 5 years of relevant sales experience, preferably in a similar regulatory industry or in the Life Science sector. Experience in the Gastroenterology market is an advantage. A proven track record of achievement in the last three years is a must. Fluency in spoken and written English is a must. Strong presentation skills, including the ability to create proposals tailored to customer needs and to demonstrate effectively. Proficiency in computer applications such as Microsoft Office and CRM platforms. Willingness to travel domestically and internationally, approx 25% of the time - mostly international. For full job spec and information please send your CV to [emailprotected] or call Linda at 01 2784703. Thornshaw Scientific is a division of the CPL Group of companies. #J-18808-Ljbffr

Overview PM Group is an international project delivery company operating across Europe, the USA and Asia. We provide project management, process design, facility design, construction management, and commissioning and qualification services for our leading multinational clients. In addition to managing large-scale one-off projects, at PM Group we also provide an OTS (Outsourced Technical Services) offering where we supply our clients with contract Engineers for their capital projects. At present, we are looking for a number of Electrical Engineers for multiple complex projects who will be site-based in our client facility based in Co. Wicklow. If you were to join the team, you will be involved in the following activities: Responsibilities Prepare detailed scope for projects, based on Manufacturing/Process area requests and apply value engineering where possible. Identify and evaluate MCC’s/Electrical installations, integrity and efficiency improvements. Define Electrical requirements for capital projects and interact with internal & external stakeholders, vendors and contractors. Project execution will focus on safety, schedule, and cost management adherence while complying with good engineering practices, company policies, and all applicable regulations and codes. Coordination with Construction Management and equipment vendors. Strict adherence to safe working practices as set out in the safety statement and other company safety rules. Manage Electrical projects throughout the project lifecycle. Ensure compliance with the clients' Procedures and Standards. Install and commission GMP and non-GMP, manufacturing and utility systems. Actively support the Validation / Qualification of GMP equipment. Work with Manufacturing, Engineering and Quality departments to troubleshoot issues. Qualifications To be successful in this role, you will have: A relevant 3rd level degree in Electronic, Electrical, Instrumentation. Experience in delivering Electrical projects in a complex Manufacturing Facility within a highly automated GMP production environment (c. 8 - 10 years). Ability to read, understand and fault find: Electrical schematics/systems during FATs or on-site commissioning. Knowledge and Experience of Hazardous area and ATEX requirements would be advantageous. Instrumentation, automation & control knowledge with project upgrade experience of PLC’s / BMS / SCADA / DCS (HVAC BMS upgrades / Process Safety upgrades, etc.). Strong understanding of the principles of current Good Manufacturing Practices (cGMP). Excellent communication / organisation skills with an ability to communicate effectively with all levels of the organisation from project teams to site leadership team. Strong computer MS Office skills (PP, Word, Excel, etc.). This is an immediate requirement; we look forward to hearing from you. #J-18808-Ljbffr

Assists in the development and implementation of injection moulding processing methods and controls to meet quality and yield required for new and existing mould tools. Identifying and implementing continuous improvements projects eliminating waste in the manufacturing process. Monitors the moulding process; troubleshooting problem process and assists in resolving quality issues and ensuring robust correction in place to prevent re-occurrence. Key Responsibilities and End Result Responsible for the Moulding Process Systems, including setting sheets, process control, deviation and control of setting sheets, ECNs and A3s. Troubleshooting and supporting daily moulding operations as required. Liaising with Toolroom, Maintenance, Operations and Quality on a daily basis. Ensuring strong systems are developed and in place to prevent defects, reduce waste and drive continuous improvement in line with company lean program. Manage Right-first-time, Moulding Scrap and moulding OEE metrics. Develop/implement maintenance programs for moulding and ancillary equipment. Training of all Team Leaders/process technicians to ensure that they are equipped to complete daily operational mould tool specific tasks (Tool face cleaning, start up/shut down etc). Assist with the introduction of new mould tools, ensuring that system/process are in place to support day to day running of the tool. All activities to be performed in strict accordance with the Quality Management System. Experience with NCMR/NCE/8D process. Other responsibilities may be assigned from time to time as needed, based on the evolution of the company and the requirements of the department. Job Specifications Degree or equivalent qualification in Polymer / Mechanical / Manufacturing engineering. 1-2 years’ experience in manufacturing environment, preferably medical device injection moulding. Lean Six Sigma skills an advantage. Familiar with process set up and validation, including performing process window studies, IQ, OQ, PQ highly desirable. Ability to work in a team environment. Excellent organizational, communication and presentation skills. Systematic troubleshooting skills. Proficient in MS Office applications, MS Project. #J-18808-Ljbffr