Job Description Fresh Food Counter Manager Advance your career with Dunnes Stores Dunnes Stores is Ireland's leading retailer positioned at the cutting edge of food and fashion retailing. If your skills, experience, and qualifications match those in this job overview, do not delay your application. We are known for offering a wide range of high quality products to our customers. With a strong brand presence and a loyal customer base, we pride ourselves on creating memorable experiences that resonate with our customers. Over the last 5 years, we have delivered an extensive rollout of new contemporary fresh food delis throughout Ireland. We plan to continue this rollout with the introduction of more Baxter & Greene Market Delis and Dunnes Stores Market Delis across the country. Both brand offers an increased product range in stores, at great value, all with improved customer service and expertise. As a Fresh Food Counter Manager with Dunnes Stores, you'll have the opportunity to grow your culinary skills and advance your food career within a nationwide retailer. You'll also receive a Dunnes Stores employee discount from your very first day. The Role The primary function of the Fresh Food Counter Manager is to take accountability for the fresh food counter which includes seafood. This role will see you delivering exceptional customer care, meeting operational standards to maximise sales and profitability, all while maintaining costs alongside the store management team. Key Responsibilities Working as part of the team with Store Management to provide the highest standard of food preparation, merchandising, and customer service. Leading, training, and developing the team in a manner appropriate to the Brand to deliver the agreed business strategy and the "Dunnes Stores Experience" customer service programme. Monitoring and delivering the HACCP programme within our fresh food counters to ensure effective standards in line with hygiene and quality regulations. Developing an efficient cleaning schedule that ensures the regular systematic cleaning and maintenance of equipment. Placing product orders with agreed suppliers on a daily basis, in a cost effective way. Monitoring and addressing any variations to the cost base of the department on a week to week basis. Delivering the budgeted KPI plan for the department and any subsequent forecasts. Maximising sales through the analysis of sales data, department trading patterns, and by pre-empting customer needs and demands. Ensuring products are prepared following agreed procedures. Coaching your team to be passionate and knowledgeable about sales, product availability, stock control, merchandising and display standards, variation prevention, pricing, ticketing, inventory, hygiene, and most importantly customer service. Ensuring all process and business changes are implemented as per the business requirements and on time. Alongside the team, adhering and complying with all relevant company policies and procedures. Being constantly on the lookout for innovative ideas inside and outside of the business. Providing feedback to senior managers on performance, key customer service developments, and operational issues. Requirements To apply for this role you must have previous experience in deli/fresh food management as well as be experienced and trained on HACCP with an in-depth knowledge of Food Safety legislation. Previous experience as a chef or in food production is preferable. You will also have: The ability to follow pre-determined recipe cards/set procedures. Excellent communication, coaching, and interpersonal skills. Excellent attention to detail, organisational skills, and the ability to multi-task. Flexibility and the ability to work as part of a team or individually. A passion, flair, and attention to detail for food production and presentation. Above all else, our Fresh Food Counter Managers have excellent product knowledge as well as problem solving, decision making, merchandising, and people management skills. Benefits: Competitive pay and an employee discount from your first day. Opportunities for professional development and career growth. A dynamic and collaborative work environment focused on innovation and growth. xsokbrc Dunnes Stores is an Equal Opportunities Employer.

TTM currently recruiting a Consultant Paediatrician s.i Pallative Medicine to one of the HSE hospital in Ireland starting ASAP. Do not miss out on this interesting and challenging opportunity to work as a Consultant Paediatrician , apply now or call or Whatsapp Roisin McSweeney at 086 084 0063 today. Requirements Full IMC Specialist Registration Membership / Post-Graduation IELTS/OET if applicable Why choose TTM to help find your new job? Dedicated Recruitment Consultant available to assist with all queries We recruit across the UK and Ireland so you will have visibility on all jobs. #J-18808-Ljbffr

TTM currently recruiting a Consultant Ophthalmologist Doctor to one of the HSE hospital in Ireland starting ASAP. Do not miss out on this interesting and challenging opportunity to work as a Consultant Ophthalmologist , apply now or call or Whatsapp Roisin McSweeney at 086 084 0063 today. Requirements: Full IMC Specialist Registration Membership / Post-Graduation IELTS/OET if applicable Why choose TTM to help find your new job? Dedicated Recruitment Consultant available to assist with all queries We recruit across the UK and Ireland so you will have visibility on all jobs #J-18808-Ljbffr

A healthcare recruitment agency is seeking a Consultant Paediatrician for a challenging role in a HSE hospital located in Waterford, Ireland. The ideal candidate must have Full IMC Specialist Registration and relevant postgraduate qualifications. This role offers an exciting opportunity to contribute to palliative medicine, with support from a dedicated recruitment consultant. If interested, apply now or contact Roisin McSweeney at 086 084 0063. #J-18808-Ljbffr

A leading healthcare recruitment agency is seeking a Consultant Ophthalmologist for one of the HSE hospitals in County Waterford, Ireland. This is a unique opportunity for a medical professional to engage in a dynamic environment starting ASAP. The successful candidate must possess Full IMC Specialist Registration, and qualifications such as Membership/Post-Graduation and IELTS/OET may be required. Don't miss out on this chance; apply now or contact our recruitment consultant for more details. #J-18808-Ljbffr

Lynch Truck Center has a rare opportunity to join our team as a Marketing & Digital Content Manager. As the Marketing & Digital Content Manager, you will be responsible for driving leads, improving inventory movement, and managing digital marketing efforts across website, social, and content channels. Who We Are Lynch is a family-owned group of Automotive Dealerships and Commercial Truck Centers that has been operating for over 65 years. Lynch offers competitive compensation packages, as well as the best benefits in the industry. What this means for you is lower premiums, lower deductibles, and better overall coverage. As we continue to grow our business, we also grow our biggest asset—our talented staff! We have countless internal promotion and advancement opportunities for you to further your career. Benefits Join a family-owned company with family values! Lynch is proud to offer industry leading income and benefit opportunities: Health Insurance, covering 100% preventative care, starting at $140/month for single coverage and $570/month for family coverage $0 copay through an independent clinic for Lynch Health Plan participants 401K with a company match of $0.30 cents on the dollar up to 5%, plus a fiscal year end discretionary match that in previous years was an additional 1.5% Dental & Vision Coverage Company paid Short Term Disability & Life Insurance, LTD Insurance, FSA, Employee Assistance Program, Wellness program, Gym Membership Discount, PTO & Holiday Pay, Bereavement Pay, Employee Parts & Service Discount, Employee Vehicle Discount, and Referral Bonus Part-Time Employees are eligible for: 401K, Employee Assistance Program, Referral Bonus, and Employee Parts & Service Discount Key Responsibilities Manage and maintain company websites (Liferay + WordPress) Optimize inventory listings and improve SEO and conversion Create content across web, social, and email Capture photo and video of inventory Partner with sales to promote inventory and drive leads Track performance and improve marketing results Requirements 3+ years marketing or digital experience Experience with website management platforms similar to WordPress or Liferay Strong written and communication skills Content creation experience (photo & video) Ability to work independently and drive results #J-18808-Ljbffr

Cambrex Corp. in Waterford is looking for a Quality Lead to enhance its Quality department. This pivotal role involves ensuring compliance with internal and external Quality Management System (QMS) requirements and continually improving the QMS. The ideal candidate should possess a Level 7 or 8 qualification in a relevant field and over 5 years’ experience in a GxP regulated environment. This is a full-time, permanent position with a commitment to quality and continuous improvement. #J-18808-Ljbffr

A leading enterprise software provider is seeking a Software Support Engineer for Podman Desktop based in Waterford, Ireland. The candidate will deliver expert support across RHEL, Windows, and Mac operating systems, utilizing diagnostics and troubleshooting techniques. Key qualifications include a strong understanding of container concepts, proficiency with Podman CLI, and excellent communication skills. This hybrid position offers an inclusive work environment and encourages a diverse range of applicants. #J-18808-Ljbffr

Purpose The Regulatory Affairs Department is responsible for managing products manufactured at Waterford from a regulatory perspective; ensuring submissions are submitted ontime, assessing change controls and deviations and ensuring regulatory compliance. Main responsibilities Maintenance of, and variations to, CMC Dossier for assigned products. Support and manage all regulatory requests impacting site products including coordination of site expert responses to support GRA in conclusion of request for information (RFI) activities as a result of deficiency letters (DLs) received from respective Health Authorities (HAs). Assess the regulatory impact of proposed changes by site for assigned products. Review and approval of Quality documentation including (but not limited to): batch records; specifications; plans; protocols/ technical reports; Standard Operating Procedures (SOPs), deviation assessments, and failure investigations for assigned products, as appropriate. Second RSO review for submission documentation. Track all site regulatory activities in real time within the site planning tracking tools. Monitor submission/approval status and track updates for assigned products. Participate in regulatory inspections/audits. Initial BLA/MAA authoring/coordination, as appropriate. Product Registration Renewals. Annual Reports e.g. US, Canada, Brazil. Periodic Quality Reviews (PQR). Contribute in project teams and provide regulatory guidance/ support. Takes ownership of product-related meetings i.e. core meeting on site/meeting with GRA/RSO counterparts in sister sites. Qualifications/Experience Experience: preferably 2 years+. Soft skills: Problem Solving, effective communication, critical thinking and time management. Technical skills: Experience of Regulatory Affairs, Manufacturing and/or Quality Operations, dealing with Health Authorities and working through corporate structure is desirable. Education: Degree in Science, Pharmacy or related discipline is essential. Languages: English. #J-18808-Ljbffr

Company Information You Matter to Cambrex. Cambrex is a leading global contract development and manufacturing organization (CDMO) that provides drug substance development and manufacturing across the entire drug lifecycle, as well as comprehensive analytical and IND enabling services. With over 40 years of experience and a team of 2,000 experts servicing global clients from North America and Europe, Cambrex offers a range of specialized drug substance technologies and capabilities, including continuous flow, controlled substances, liquid‑phase peptide synthesis, solid‑state science, material characterization, and highly potent APIs. Your Work Matters. At Cambrex, we strive to build a culture where all colleagues have the opportunity to: engage in work that matters to our customers and the patients they serve learn new skills and enjoy new experiences in an engaging and safe environment strengthen connections with coworkers and the community We’re committed to attracting and nurturing a passionate team of valued professionals in our fast‑paced and growing company. We offer a competitive benefits package that includes healthcare, life insurance, planning for retirement, and more! Your Future Matters. Known for our customer‑focused scientific and manufacturing excellence, as well as our strong commitment to quality and safety, we offer a range of career and growth opportunities across our global network of locations. Together with our customers, we aim to improve the quality of life for patients around the world. Start a career where You Matter by applying today! Job Overview We are seeking applicants for the position of Quality Lead to join our team. This role will report directly to the Quality Manager for Waterford and will be a pivotal role in our growing Quality department. Responsibilities Key Responsibilities: Provide expert guidance and support to the Company on all Quality Management System (QMS) activities. Ensure all company operations comply with internal QMS requirements and applicable cGMP, GxP, and ISO standards. Maintain, monitor, and continuously improve the QMS by identifying risks, proposing enhancements, and driving corrective and preventive actions (CAPAs). Oversee the administration and maintenance of quality manuals, procedures, and records, and lead continuous improvement initiatives in collaboration with management. Ensure all planned and unplanned changes, deviations, and non‑conformances are appropriately investigated, documented, and closed in line with regulatory expectations. Plan, conduct, and report internal audits to ensure ongoing compliance with GxP and ISO certification requirements. Serve as the Quality Lead for all internal, regulatory, supplier, and customer audits, including audit preparation, hosting, follow‑up, and closure of audit findings. Quality Documentation & Administration Responsibilities Manage controlled documentation within the QMS, including the issuance, revision, and archiving of quality documents such as logbooks, protocols, and forms. Maintain document control systems and indexes (electronic and hard copy), including document numbering and version control. Review completed quality documents to ensure accuracy, completeness, and compliance with approved specifications and procedures. Propose, review, and implement document changes as required to support operational and regulatory needs. Verify second‑person reviews and signoffs for operational documentation where required. Provide Quality oversight support for operational activities. Perform daily checks of stability cabinets and controlled room conditions when required. Supporting sample receipt, inspection, and dispatch activities as appropriate. Deliver general quality and administrative support as needed. Qualifications/Skills Hands on experience with core Quality system activities such as Deviations, Investigations, Document Management and Audits. Understanding of regulatory inspection readiness and data integrity principles (ALCOA+) A proactive self‑starter with strong organisational skills, capable of independently managing priorities and delivering high‑quality work to deadlines. Excellent communication skills, with the ability to present complex information clearly and confidently to both team members and management. A collaborative, team‑focused mindset, committed to building strong working relationships and performing effectively in a fast‑paced environment. Hours of Work This is a full time, permanent position Hours are 8.30am to 5pm, Monday – Friday Education, Experience & Licensing Requirements Level 7 or 8 qualification in a relevant discipline such as Quality, Science, Chemistry, Biotechnology or related field. Equivalent combination of education and experience may be considered. Minimum of 5+ years’ experience working in a GxP regulated environment, including experience leading Quality activities, projects or junior team members. Cambrex is committed to providing a safe and productive work environment. All offers of employment are contingent on the successful completion of a comprehensive pre‑employment screen. The pre‑employment screen may consist of several components including but not limited to a drug test, criminal record check, identity verification, reference checks, education and employment verification, and may vary based on federal, state, and local laws. Refusal to submit to testing will result in disqualification of further employment consideration. All requirements are subject to possible modifications to reasonably accommodate individuals with disabilities. Cambrex Corporation is an Equal Opportunity / Affymative Action employer and will consider all qualified applicants for employment without regard to race, color, religion, sex (including pregnancy, sexual orientation, or gender identity), ancestry, national origin, place of birth, age, marital status, disability/handicap, genetic information, veteran status, or other characteristics protected by federal, state, and/or local law. #J-18808-Ljbffr