Location: Based in Kilcoole, Co. Wicklow. Hours: 9 Hours per day AJ Products Ireland are looking for a skilled and reliable Product Assembler and Delivery Driver to join our team. AJ Products have been delivering white glove service to all our customers all over Ireland for nearly 19 years. This role primarily focuses on the assembly of office furniture and warehouse racking, with a keen eye for detail, and a commitment to delivering high-quality customer and assembly services. Additionally, you will be responsible for safely transporting products to customer locations and ensuring a positive delivery experience. Key Responsibilities: Product Assembly: Assemble a wide range of products on-site at customer locations, following detailed manufacturer instructions and safety guidelines. Perform quality checks to ensure all assembled products are safe, functional, and meet high standards of quality. Troubleshoot and resolve any issues that may arise during the assembly process, using problem-solving skills and mechanical knowledge. Educate customers on the proper use, maintenance, and care of the assembled products, ensuring they are satisfied with the final setup. Maintain a clean and organized workspace during the assembly process, respecting the customer’s home or business environment. Delivery Driving: Safely operate company vehicles to transport products to customer locations, adhering to all traffic laws and company policies. Carefully load and unload products to prevent damage during transit, ensuring all items are handled with care. Adhere to the planned delivery routes efficiently to meet scheduled delivery times and minimize delays. Communicate effectively with customers to provide updates on delivery times and ensure a positive experience. Work closely with the sales team, feeding back any information from their customers. Additional Responsibilities: Maintain accurate records of deliveries, assemblies, and any customer feedback or concerns. Conduct routine vehicle inspections and maintenance to ensure safety and compliance with regulations. Follow all company policies, procedures, and safety guidelines to maintain a safe working environment. Qualifications: Proven experience in product assembly, carpentry, or a related field is highly preferred. Strong mechanical aptitude and proficiency with hand and power tools. Excellent customer service skills with the ability to communicate clearly and professionally. Ability to read and interpret detailed assembly instructions and diagrams. Valid driver’s license with a clean driving record. Strong attention to detail and ability to solve problems independently. Physical ability to lift, carry, and assemble heavy items and perform manual tasks. Ability to manage time effectively and work independently in a fast-paced environment. Benefits: Competitive pay Comprehensive training and support provided. #J-18808-Ljbffr

An Exciting opportunity for the right candidate. Cairnhill Nursing is part of Trinity Care Group, a well-respected, multi-award-winning Nursing Home Group, part of the international DomusVi Group. Cairnhill Nursing Home aims to provide the highest quality of care and services to all Residents, above and beyond their expectations and those of their relatives. This is provided in a homely and friendly environment where Residents' privacy and dignity is respected and their individuality maintained. We provide private residential, convalescent, and rehabilitative care in our purpose-built Nursing Homes. We have centres in Dublin, Meath, Louth, Kildare, Kilkenny, Cavan, and Wicklow. We are currently looking to recruit an Activities Co-Ordinator to join our team of fantastic staff. Our Activities Co-Ordinator plays a vital role in our Residents' lives. Responsibilities: Develop and organise a range of events/activities for our Residents. Work collaboratively as a team player. Work independently and on your own initiative. Engage with Residents in a friendly, creative, and confident manner. Minimum Requirements: A genuine interest in working with our Residents. Previous experience of working with the relevant Client group. Qualification in remedial/occupational therapies. Flexible approach towards working routines. If you are that person, please send us your CV. #J-18808-Ljbffr

VACANCY: Health and Safety Officer LOCATION: Wicklow 3DPersonnel’s client is a well-known Developer with a 4-year project in Co. Wicklow. Qualifications and Experience: Must have a Qualification in Health & Safety 2 years’ experience in the construction industry Knowledge of IT systems is an advantage Set an example of enthusiasm, loyalty, and hard work in the performance of all duties Site experience is essential If interested, apply for immediate consideration. For more info, call the poster Jason McGowan at 0861841361. #J-18808-Ljbffr

Job Title: Senior/Principal Design Quality Engineer Our Continuous Glucose monitoring device is a key pillar of growth for the organisation as we look to enter new markets with an innovative device, providing a more sustainable and accessible alternative to diabetes patients globally. To support this innovative product's development, we now require a Senior/Principal Design Quality Engineer to develop and implement compliance strategies to support New Product Introductions (NPI) and current marketed products within the areas of design, design transfer, manufacturing, and service. As a critical member of the NPI core team, you will ensure adherence to the Quality Management System (QMS) and regulatory requirements. By employing strong critical thinking and influencing skills, you will work cross-functionally to ensure robust Quality decisions. In this role, you will have a direct impact on ensuring patient safety, audit readiness and execution, and enable commercial delivery of the company's systems. This role will be responsible for both CGM and our wider product set; however, CGM is the primary focus foreseen for this role. Key Responsibilities: Developing and implementing compliance strategies to support New Product Introductions and current marketed products within the areas of design, design transfer, manufacturing, and service. Ensuring compliance to the company's QMS and regulatory requirements (e.g. 21 CFR 820, ISO 13485, MDR) while driving process effectiveness and efficiency. Ensuring plans, protocols, results, and conclusions are generated, reviewed, and approved according to applicable procedures. Lead the integration, optimisation, and ongoing development of the company's design and development processes into our eQMS. Performing internal audits, for example assessing compliance of the Design History File (DHF) and other programme files, to ensure Quality standards and regulatory requirements are addressed. Participate in external audits as the subject matter expert for design control and associated processes. Provide Design Quality Engineering oversight and lead relevant design CAPA projects and non-conformance evaluations. Maintaining product and site certifications through successful external audits. Driving audit-readiness activities and representing the company to external agencies during audits. Providing design control guidance and coaching to the wider Quality and R&D teams, partnering with them to ensure a seamless process from design through to registration. Creating the required documentation to support effective global regulatory submissions, liaising with external bodies to ensure their speedy acceptance. Leading activities to improve upon the design process within the company, seeking out best practice and implementing this into the QMS. Minimum Requirements: Bachelor's degree in a relevant scientific/engineering discipline or the ability to show technical understanding of scientific/engineering principles through industrial experience. Over 10 years of substantial expertise in Design Quality Engineering in the Medical Device industry. Experience working with regulatory and notified bodies during submissions and external audits. Excellent knowledge of design control and risk management processes. Understanding of regulatory requirements, e.g. ISO 13485/ FDA regulations. Expertise in design verification and validation methodologies. Strong knowledge of quality management systems (QMS). Proficiency in conducting design reviews. Familiarity with industry-specific design standards and best practices. Excellent communication, collaboration, and interpersonal skills. Attention to detail and a high degree of accuracy. Ability to work effectively in cross-functional teams. Strong organisational and time management skills. Adaptability and flexibility in handling changing priorities and requirements. Ability to work independently and take initiative. Leadership and teamwork skills. Continuous learning mindset to stay updated with evolving technologies and industry practices. Desired Skills and Experience: Mechanical, Design, Quality, Medical Device, ISO 13485, FDA Regulations, QMS, Verification, Validation, CAPA, 21 CFR 820, ISO 13485, MDR, Quality, Quality Management. Adecco Ireland is acting as an Employment Agency in relation to this vacancy. #J-18808-Ljbffr

Company Description Impact Engineering Ltd is a trusted automation partner, proving services to the Life Sciences sector in Ireland. We are focussed on business transformation, digitalisation, and providing innovative automation solutions. Our team combines technical and business expertise to deliver cost-competitive and compliant automation projects, aiming to maximize safety, quality, and throughput while minimizing costs and environmental impact. We offer automation services, targeted training, and control system administration to add value to your business journey into digitalisation. Role Description This is a full-time on-site role for an Automation Engineer at Impact Engineering's key client in Wicklow. The Automation Engineer will be responsible for supporting exisiting operations including; troubleshooting exisiting systems, supporting automation projects, system upgrades, and optimization efforts. The role involves collaborating with stakeholders, administering control systems, and ensuring quality assurance operations are in compliance with industry standards. Qualifications 3+ years automation experience within Life Sciences Proficiency in Wonderware and SQL required Previous experience providing support to automation batch manufacturing plants required Bachelor's degree in Engineering or related field Strong problem-solving and analytical skills Knowledge of computer system validation and quality assurance operations #J-18808-Ljbffr

My client, a global company specialising in the development, manufacture and marketing of clinical diagnostic products are hiring a Senior Process Development Engineer to join their Biosensor Division in Bray Co. Wicklow. This is an exciting and innovative opportunity for an experienced candidate working with cutting edge technology and the future of medical devices! About The Role The ideal candidate will play a critical role in developing and optimizing manufacturing processes for our continuous glucose monitoring systems. This position involves working closely with cross-functional teams to ensure our products meet the highest standards of quality, reliability, and performance. Develop and optimize manufacturing processes for CGM systems, ensuring efficiency, scalability, and cost-effectiveness. Provide technical support for the production team, troubleshooting and resolving process-related issues. Ensure processes comply with regulatory requirements and quality standards (e.g., ISO 13485, FDA). Lead and participate in continuous improvement initiatives to enhance process reliability and product quality. Manage process development projects, ensuring timelines, budgets, and deliverables are met. Requirements And Skills Bachelor’s degree in Engineering, Chemistry, Biotechnology, or a related field. Advanced degree preferred. Minimum of 5 years of experience in process development, preferably in the medical device or biotechnology industry. Proven experience with continuous glucose monitoring systems or similar technologies is highly desirable. Strong understanding of manufacturing processes, including chemical, mechanical, and electronic assembly. Proficient in using process development tools and software (e.g., CAD, Minitab, statistical analysis tools). Familiarity with Good Manufacturing Practices (GMP) and regulatory requirements for medical devices. Six Sigma Green Belt or Black Belt certification is a plus. Relevant professional certifications (e.g., ASQ Certified Quality Engineer) are advantageous. For a full Job Spec and to apply for this role please call Katie on +353 1 895 5770 or e-mail [email protected] Thornshaw Scientific Recruitment is a leading Irish provider of specialist Scientific Recruitment. Part of the CPL Group. www.thornshaw.com Tel: +353 1 895 5770 #J-18808-Ljbffr

Job Description Consistent delivery of Shoreline Leisure’s “Member Promise” when dealing with all centre patrons. Rostering consists of early morning & evening shifts. The occasional weekend shift if required. Responsible for dealing with membership transactions, handling cash as well as daily administration duties. Responsible for daily management of the centre's membership system, monthly cancellations, membership suspension requests, preparation of monthly direct debit file. Responsible for follow-up communications with clients in relation to outstanding account payments. Maintaining daily membership logs and end of month membership reports. Working alongside centre senior managers in relation to outstanding annual membership renewals. Managing all incoming/outgoing member communications to the standard expected by Shoreline Leisure. Checking daily float and finalising end of shift cash audit making sure all income balances with the X reading and Sage export reports. Responsible for dealing with any member complaints and other possible issues arising during your shift in the absence of senior management. General retail duties as required. Ordering and maintaining stock levels of goods for resale. Developing new revenue opportunities. Maintaining a high degree of customer care whilst dealing with the public. Responsible for working as part of the team in regard to the overall hygiene of the club and reporting any issues to the manager on duty. To assist the managers with the induction and training of future staff in normal operational procedures and emergency action plans. Organising Sports Group Bookings and Events. Assisting with marketing the site. Working in a team environment with the General Manager, Assistant Manager, Duty Manager and Full/Part-Time staff where work will be delegated, and deadlines will have to be adhered to. Partake in any personal development and/or training workshops as requested by management. Such other duties as may be assigned from time to time. Job Type: Full-time Pay: €12.85-€12.90 per hour Expected hours: 40 per week Benefits: Bike to work scheme Company pension Gym membership On-site gym On-site parking Sick pay Schedule: 8 hour shift Weekend availability Experience: Reception / Administration: 1 year (preferred) Language: English (required) Work Location: In person Application deadline: 31/07/2024 #J-18808-Ljbffr

Pharmacy Technician - Greystones, Co. Wicklow (40 hours a week) A full-time position which would suit an organised person. This is a 40-hour permanent contract. The main duties of this role will include the following: To operate the dispensary following all the legal responsibilities of the profession of pharmacy To exercise all aspects of law, ethics and codes of practice as laid down by the Irish Pharmaceutical Society. To provide a safe and efficient dispensing service to all customers following company guidelines. To ensure the safe and effective delivery of medicines to all customers To interact with other health professionals Active management of the monthly submissions to payment boards Pro-active management and follow-up of the claims rejected To build and maintain relationships with local doctors and other health professionals Essential Criteria IPU Pharmacy Technician course or Higher Certificate in Pharmacy Technician Studies essential Ability to read, write, and speak English fluently with excellent communication skills, both orally and in writing. Benefits Include Monthly performance bonus Maternity & paternity pay Sick pay Service-related pay increases Generous staff discounts in-store Additional service days Excellent referral scheme Tax-saver travel schemes. For further details, please contact Brian on 086 7773856 Pharmacy Technician, Pharmacy, Community Pharmacy Technician, Technician, Pharmacy, Wicklow #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 About the role This is a management position in an ethical Solid Oral Dosage Pharmaceutical Formulation and Finished Product plant. The brief requires a thorough knowledge of Good Manufacturing Practice, current FDA & EMEA regulations for solid oral dosage pharmaceuticals for human use and a good working knowledge of manufacturing processes, packaging processes and validation activities used in the pharmaceutical industry. Good organizational, supervisory, Technical Writing And Investigation Skills Are Required. How you will contribute Act as the formal contact point with the HRPA, the FDA and other Regulatory Authorities. Promote a culture of Compliance, Right First Time and Continuous Improvement. Implement efficiency improvements in Quality and participate in site projects and initiatives. Management and oversight of site Regulatory Compliance and oversee the Contract Manufacturing Business Quality activities for the site. Inspection Management: Prepare and present the Company for both immediate and routine Regulatory Inspections. In addition, you may be involved in attending or conducting overseas facility inspections. Manage and maintain site self-inspection program. Oversight of Annual Product Quality Reviews. Quality data management in SAP and XFP (MES). Management of customer, supplier and service agreements. Oversight of GMP processes (Pest control, contamination control, facility/utility monitoring/requalification etc.). Oversight of GxP processes (system data integrity, periodic and backup reviews). Support the site Quality Management systems including the Deviation and CAPA Management systems, Change Control system, GMP Training and the Vendor Management program. Oversight of validation lifecycle, including documents and associated deviations/NCRs for equipment, facility, utility, process, cleaning & computerized systems in line with current industry regulations and guidelines. Oversight of Quality risk Management program at site. Acting as a designee to the Site Quality Head as required. General Responsibilities Drive and promote the corporate values of Takeda-ism within the workplace. Actively foster, in cooperation with other TIL staff, an ethos and culture of safety awareness where safety is accepted as an integral part of the overall business. Drive and maintain staff development. Drive and Maintain Department KPIs. Drive and support site must win battles. Other duties as required and directed by the Site Quality Head, or other Officer appointed by the Board of Directors. What You Bring To Takeda Degree in Science or other relevant field. QP Qualification desirable but not necessary. At least 3 years’ experience working in a Quality or Engineering Management role in a regulated environment. Experience in audit management (HPRA, FDA, Corporate and Clients). Previous experience in Lean Management is preferable. Good knowledge of Pharmaceutical Production & Packaging processes. Solid Oral Dosage processing experience is highly desirable. Good knowledge of GMP, validation regulations and guidelines is highly desirable. A strong technical understanding of processes, equipment and computer systems is advantageous. Experience in data integrity practices would be an advantage. Qualified Person status is desirable but not essential. What Takeda Can Offer You Great compensation package and performance-based bonus. Employer retirement plan contributions. Employee Stock Purchase Plan. Revenue approved profit share scheme. Employer funded income protection. Employer funded private medical insurance with dependants' cover. Employer life insurance contributions. Electric charging points available at parking locations. Employee Assistance Program. Wellbeing and engagement teams. Takeda Resource Groups. Flexible schedule, e.g., hybrid or shiftwork with shift allowance. Family friendly policies. 26 vacation days plus additional days for service milestones. Educational programs and formal training. Development opportunities. Humanitarian volunteering leave options. Subsidized canteen. Flexible employee funded options like Dental Insurance, Partner Life Insurance, Serious Illness Protection, Fuel Card, Bike to Work, Commuter Ticket, and Insurance Deals. More About Us Takeda is focused on creating better health for people and a brighter future for the world. We aim to discover and deliver life-transforming treatments in our core therapeutic and departments, including gastrointestinal and inflammation, rare diseases, plasma-derived therapies, oncology, neuroscience, and vaccines. Takeda Ireland was established in 1997. Our story in Ireland is one of substantial growth, rapid change, and over the past two years, Takeda Ireland has invested over €55 million in Ireland to develop our manufacturing sites, solidifying our commitment to our people and contributing to the local economy. Takeda in Ireland has commercial operations, corporate services, and manufacturing facilities across four locations: Baggot St, Bray, Citywest, and Grange Castle. We have been certified as Top Employer for several consecutive years. How We Will Support You Takeda is proud of its commitment to create a diverse workforce and to provide equal employment opportunities to all employees and applicants for employment without regard to ethnicity, colour, 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 living with disabilities, chronic illness, or neurodiversity, please feel free to let us know so that we can provide you with appropriate support during the application process. Locations Bray, Ireland Worker Type Employee Worker Sub-Type Regular Time Type Full time #J-18808-Ljbffr

A fantastic opportunity has arisen for an experienced Maintenance Manager to join the dynamic team at Druids Glen Resort. Reporting to the Hotel Manager, the successful candidate will manage the maintenance team and ensure a high standard and upkeep of all areas of the resort. Druids Glen Resort is situated in County Wicklow, only 20 miles south of Dublin. The hotel is carefully sited in a beautiful landscaped estate and allows spectacular views across the Druids Glen Golf Course and Druids Heath Golf Course. The hotel comprises 145 luxury appointed bedrooms including 11 suites. For dining and entertainment, the hotel offers many options as well as a health spa and fitness facility with pool, gym, and a fully serviced conference centre. Our stunning lounge overlooks the 13th hole of Druids Glen Golf Course. The success of any hotel comes, not with the decor and elaborate rooms, but from the friendliness and courtesy of the associates it employs. The success of Druids Glen Resort, we believe, depends on the commitment of each member of the team to practice teamwork, mutual respect, responsibility, and professionalism. Main Functions: You will continually support and improve engineering services that effectively address problems affecting guests and associates. Ensure all repairs are completed in a timely manner. You will be responsible for ensuring that all equipment is kept in good repair. Motivate and lead staff members. Maintain resort standards, policies, and procedures. Plan, control, and organise all maintenance activities in the resort. Ensure preventative maintenance is completed throughout the resort. The ideal candidate: Will have general maintenance experience in: Equipment upkeep Painting Plumbing Air Handling Units & BMS Previous experience working within the area of Electrical & General Maintenance. Excellent communication skills are a must as you will be required to communicate with hotel guests and fellow employees on a consistent basis. A third-level qualification to a minimum standard of a Higher Certificate (QQI) (Level 6) in a building discipline or relevant engineering discipline or fully served Trade apprenticeship of not less than four years. Have 5 years post qualification/apprenticeship (electrical or mechanical or similar) experience of maintaining industrial and domestic type buildings, of which 2 years' experience must be in the management of a maintenance team. In return we offer excellent employee benefits including: Complimentary Health Club and pool membership. Complimentary golf on both Druids Glen and Druids Heath courses. Discounted golf and health club rates for friends and family members. Career Development and Training. Rewards for personal achievement in sport. Rewards for personal achievement in education. Rewards for personal achievement in community activity. Length of Service Rewards. Internal Training Rewards. Upselling & Other Departmental Rewards. Discounted Spa treatments. Educational Assistance - for Hospitality & other professional courses. Bike to work scheme & other commuter plans. Meals during shifts. Free on-site tea/coffee. Free parking. Healthy Snacks. Staff Discounts on accommodation in our Sister Properties. Opportunities for advancement & Career Development. Achievers of the Year. Leaders of the Quarter. Achievers of the Month. Departmental Star of the Month. X-points Reward Catalogue. Employee Referral Bonus. Financial Planning Resources. Team & Departmental Rewards. If you have previous experience and would be interested in the opportunity of career advancement within a 5 Star property, contact us today. Druids Glen is an equal opportunities employer. #J-18808-Ljbffr