Candidates

Senior Buying Manager

Dublin FMCG & Food Production

Ref: JOB-14136_1747408746

Senior Buying Manager Location: West Dublin | Sector: Retail & Builder Providers | Type: Permanent An established builder providers and retail group, recognised as a market leader in its field, is looking to recruit a Senior Buying Manager to take ownership of one of its largest and most commercially critical categories - bathrooms. This is a key role in the business, suited to a commercially astute buying professional with strong retail or hardware experience, who can drive performance, manage key supplier relationships, and ensure a best-in-class product offering for customers. Key Responsibilities: Supplier Negotiation: Build and manage strong relationships with manufacturers and distributors. Negotiate pricing, terms, and service levels to secure competitive advantage. Product Selection: Identify, source and select a broad range of products aligned with customer needs, market trends, and category strategy. Stock Management: Collaborate with internal teams and external partners to maintain optimal stock levels and availability across all channels. Market Analysis: Monitor competitor activity and market trends to inform buying decisions and identify opportunities for growth within the category. Experience & Profile: 8-10 years' experience in a retail or hardware buying role. Previous experience managing the bathroom or sanitary category is highly desirable. Proven track record in supplier management and commercial negotiation. Strong commercial acumen with the ability to balance cost, margin, and customer value. Confident communicator with the ability to influence at all levels. What's on Offer: Competitive salary and benefits package. Career development opportunities within a respected, high-performing business. This is an excellent opportunity to step into a high-impact role within a well-established, growth-focused organisation. The Next Step for you: Should this position be of interest to you please forward your CV to Sarah Mac Mullan from Next Generation Recruitment or alternatively call on the main line on 00 353 1 6498546 Next Generation are specialists in Supply Chain, Procurement, Engineering, Quality, Technical and Operation (permanent, contract and temporary) positions. Applications are in strict confidence. Next Generation will never share your data outside of our organisation without your prior written consent. Please read our Data Protection Policy on our website.

Senior Quality Engineer

Wicklow Pharmaceutical Recruitment

Ref: JOB-14135_1747398145

Are you a proactive quality professional ready to take the lead in driving compliance and continuous improvement in a dynamic medical device environment? My client is looking for a Senior Quality Engineer to join their team and play a critical role in upholding the highest standards of quality and regulatory compliance. Key Responsibilities Lead and manage root cause investigations, NCRs, and CAPA implementation to ensure timely and effective resolutions. Support the Quality Assurance Manager with day-to-day Quality Management System (QMS) operations in line with ISO 13485 and applicable regulatory requirements. Conduct and support internal audits to drive ongoing compliance and continuous improvement. Oversee and support validation activities, including process and test method validations, and risk assessments. Provide hands-on quality support to manufacturing, ensuring product compliance and robust process control. Develop, implement, and maintain SOPs and work instructions that align with quality initiatives and operational needs. Act as a key liaison for customer complaints and regulatory inquiries, leading investigations where necessary. Champion continuous improvement initiatives to enhance efficiency and product quality. Mentor and support junior members of the quality team, fostering a culture of learning and growth. Support supplier quality management, including the establishment of quality agreements and compliance monitoring. Own and manage preventive maintenance and calibration schedules. Assist with the ongoing development and training of the broader quality team. Requirements Bachelor's degree in Engineering, Quality, Life Sciences, or a related discipline. 5+ years of experience in a medical device or regulated manufacturing environment. Proven expertise in root cause analysis, CAPA systems, and failure investigations. Internal auditor training in ISO 13485 (Lead Auditor certification is a plus). Solid knowledge of quality engineering tools: FMEA, SPC, risk management, and validation practices. Strong analytical and problem-solving skills with a data-driven approach. Excellent interpersonal and communication skills with a collaborative mindset. Proficiency in Microsoft Office Suite and experience with quality management software. The Next Step for you: Should this position be of interest to you please submit your CV to Barry O'Mahony from Next Generation Recruitment using the apply button. Next Generation are specialists in Supply Chain, Procurement, Engineering, Quality, Technical and Operation (permanent, contract and temporary) positions. Applications are in strict confidence. Next Generation will never share your data outside of our organisation without your prior written consent. Please read our Data Protection Policy on our website.

Buyer

Dublin Supply Chain and Logistics

Ref: JOB-14128_1747150641

Job Title: Buyer Location: West Dublin (with travel to site) Industry: Construction Experience: 2-3 years in Purchasing/Buying Licence: Full, clean Irish driving licence required Overview: We are working with a leading construction company based in West Dublin to recruit a Buyer to join their team. This is a permanent role offering strong progression potential within a well-established business. Key Responsibilities: Manage procurement of materials, plant and equipment for ongoing projects Source and negotiate with suppliers to ensure best value and timely delivery Monitor stock levels and ensure site teams have what they need Maintain strong supplier relationships and keep accurate records Liaise with project managers, site teams and internal departments Conduct regular site visits (travel required) Requirements: 2-3 years' experience in a purchasing or buying role Strong interest in construction, engineering or similar technical fields Full, clean Irish driving licence Excellent communication, organisation and negotiation skills Ability to work independently and as part of a team Desirable: Experience in construction or a related industry Familiarity with procurement software or systems

Quality Supervisor

County Meath FMCG & Food Production

Ref: JOB-14126_1747137435

Now Hiring: Quality Supervisor - Fresh Produce I'm working with a leading food production company who are looking for an experienced Quality Supervisor to step into a critical, hands-on position within their quality team. If you thrive in a fast-paced, production-focused environment and have a solid background in HACCP, traceability, and quality leadership, this could be the right opportunity for you. What you'll be doing: Taking charge of day-to-day floor-based quality checks. Leading and supporting a small QC team and working closely with the wider technical and production teams. Maintaining and monitoring traceability systems, ensuring products meet the highest quality and food safety standards from intake to dispatch. Liaising with QC staff, production operatives, and line leaders to manage customer complaints, labelling accuracy, and packing quality. Supporting internal and hygiene audits and maintaining compliance with HACCP, CCPs, BRCGS (V9) and Bord Bia standards. Playing a key role in supplier performance tracking, internal quality reporting, and product issue resolution. What we're looking for: A degree in Food Science or a related discipline. 3-5 years' experience in the fresh produce or food manufacturing sector. Strong HACCP (Level 3) and traceability experience. Confident understanding of critical control points (CCPs) and quality reporting. A proactive, hands-on individual with strong communication and attention to detail. Previous experience in audit preparation is highly desirable. Must have a full driving license and own transport. The next step for you: Should this position be of interest, please apply with an up-to-date CV to Jessica from Next Generation Recruitment or call us on the main line at 016629120. Next Generation are specialists in Supply Chain, Procurement, Engineering, Quality, Technical, and Operation positions (permanent, contract, and temporary). All applications are handled in strict confidence. We never share your data outside of our organization without your prior written consent. For more information, please review our Data Protection Policy on our website.

Qualified Person

Dublin Pharmaceutical Recruitment

Ref: JOB-14113_1747122076

Qualified Person Key Responsibilities: Serve as Qualified Person (QP) for the certification and batch release of clinical trial supplies in compliance with EU regulations. Act as Responsible Person (RP) on the Wholesale Distribution Authorisation (WDA) for Pre-Approval Access activities. Support regulatory authority inspections and audits (GMP/GDP) across the global clinical and commercial supply chain. Advise cross-functional teams on quality issue management, regulatory compliance, and continuous process improvement. Monitor and integrate global regulatory trends, ensuring quality systems and operations remain compliant and efficient. Maintain and update Site Master Files and Manufacturing Authorisations. Escalate and communicate significant quality issues or deviations promptly to stakeholders and senior management. Review, approve, and manage procedural and quality documentation. Actively contribute to cross-functional project teams and strategic working groups within Quality and Supply Chain functions. Provide expert guidance to ensure alignment with external regulations and internal policies at global and cross-functional levels. Represent the organization in interactions with regulators, trade bodies, and professional associations to influence industry practices and policies. Identify quality and compliance risks and contribute to mitigation planning. Offer input into the development of global audit programs, informed by trends, risk signals, and compliance gaps. Pursue continuous professional development, including site visits, training, and audit participation. Support Operational Excellence (OPEX) initiatives and champion continuous improvement in quality systems and culture. Required Qualifications & Experience: Bachelor's degree (or higher) in a scientific, engineering, or related discipline. Minimum of 10 years' experience in the pharmaceutical or biopharmaceutical industry. Eligible to act as a Qualified Person (QP) under EU directives on the Manufacturing/Importation Authorisation. Previous experience as a Responsible Person (RP) under a WDA is strongly preferred. In-depth knowledge of ICH guidelines, GMP/GDP standards, data integrity principles, and clinical supply chain operations. Demonstrated success in building and leading high-performing quality teams and working effectively across global, cross-functional environments. Excellent communication skills with a proven ability to influence, engage, and drive results across matrixed and international teams. Strong leadership qualities and commitment to fostering a culture of quality and continuous improvement. The Next Step for you: Should this position be of interest to you please submit your CV to Barry O'Mahony from Next Generation Recruitment using the apply button. Next Generation are specialists in Supply Chain, Procurement, Engineering, Quality, Technical and Operation (permanent, contract and temporary) positions. Applications are in strict confidence. Next Generation will never share your data outside of our organisation without your prior written consent. Please read our Data Protection Policy on our website.

CQV Engineer

Dublin Pharmaceutical Recruitment

Ref: JOB-14124_1747121676

CQV Equipment Engineer Responsibilities: Develop and execute CQV testing documentation for utility systems within a sterile drug product manufacturing facility. Deliver on key project milestones, including safety, schedule adherence, and high-quality documentation/electronic records for assigned equipment and utilities. Ensure testing of utility systems complies with Good Manufacturing Practices (GMP), internal company policies, and EU/FDA regulatory standards. Oversee commissioning of non-GMP utility systems in line with project-specific standards. Manage deviations associated with assigned systems and equipment. Conduct risk assessments related to CQV activities; develop mitigation strategies to address potential qualification risks. Support Factory Acceptance Testing (FAT), and integrate outcomes into the overall qualification strategy for equipment, facilities, and utilities. Complete all required training in a timely manner to support site compliance metrics. Collaborate with site stakeholders, vendors, and contractors to ensure smooth project execution. Perform field inspections, FAT/SAT participation, and walkdowns to confirm proper installation and operation of systems. Required Competencies: Proven ability to independently execute CQV activities from initiation through to completion. Full lifecycle CQV project experience, including design, commissioning, qualification, and handover. Strong background in CQV for sterile drug product manufacturing environments, including utility systems with integrated automation. Hands-on experience with black utility systems (e.g., compressed air, plant steam, process waste, chilled water). Excellent technical documentation and execution skills, with a strong track record of meeting project timelines. Strong interpersonal and communication skills; ability to work effectively in cross-functional teams. Demonstrated ability to contribute within a matrixed team environment and manage multiple priorities simultaneously. Qualifications & Experience: Bachelor's degree in Engineering, Life Sciences, or a related technical discipline. Minimum of 5 years of CQV experience within the pharmaceutical or biotech industry, with a focus on utility systems and sterile manufacturing operations.

Utility Engineer SME

Dublin Pharmaceutical Recruitment

Ref: JOB-14125_1747121552

The Site Utility Engineering Subject Matter Experts (SMEs) will act as Utility System Owners for Black and Clean Utilities. They will be responsible for providing engineering oversight, technical support, and continuous improvement for assigned utility infrastructure, systems, and equipment across the site. Key Responsibilities: Ensure all utility systems are compliant with applicable regulatory standards, including cGMP, cGDP, EHS, global engineering directives, and local regulations. Lead the development of User Requirements Specifications (URS) for new equipment and modifications to existing systems, collaborating closely with internal stakeholders. Maintain and update asset records, calibration data, preventive/predictive maintenance (PM/PdM) schedules, job plans, and spare parts inventory within the CMMS. Conduct root cause analyses (e.g., Cause Mapping) on chronic, critical, or high-impact equipment failures and implement corrective actions. Minimize unscheduled downtime by enhancing maintenance strategies and responding swiftly to equipment failures. Review vendor and contractor maintenance reports, initiate CMMS actions (e.g., corrective maintenance, PM, PdM) to address any deficiencies. Act as system and area owner by conducting risk assessments, leading RCA investigations, and driving CAPA implementation to prevent recurrence of issues. Own and manage change controls related to assigned utility systems. Represent utility systems as the Subject Matter Expert (SME) during internal and external audits. Establish and track key performance indicators (KPIs) for system performance, including cost, efficiency, and uptime. Develop and manage annual operating budgets and identify cost-effective system improvements or upgrades. Define scopes and provide project management support for capital projects and system modifications. Champion a culture of continuous improvement and operational excellence. Required Competencies: Proven team leadership and collaboration skills within a cross-functional, high-performance environment. Ability to deliver engineering solutions aligned with business goals and cost efficiency. In-depth knowledge of utility system design, operation, and maintenance in GMP-regulated facilities. Strong understanding of regulatory requirements, including EHS and quality compliance within pharmaceutical/biopharmaceutical environments. Prior experience representing utility systems to regulatory authorities is essential. Qualifications & Experience: Minimum of a Level 8 Bachelor of Engineering (BEng) degree in a relevant engineering discipline. At least 8 years of experience in pharmaceutical manufacturing, with a focus on utilities or maintenance engineering. Strong problem-solving skills, with the ability to take initiative and lead technical investigations and system improvements. Familiarity with CMMS systems and a structured approach to maintenance planning and execution. The Next Step for you: Should this position be of interest to you please submit your CV to Barry O'Mahony from Next Generation Recruitment using the apply button. Next Generation are specialists in Supply Chain, Procurement, Engineering, Quality, Technical and Operation (permanent, contract and temporary) positions. Applications are in strict confidence. Next Generation will never share your data outside of our organisation without your prior written consent. Please read our Data Protection Policy on our website.

CQV Engineer 62365

Dublin Pharmaceutical Recruitment

Ref: JOB-14124_1747120915

CQV Equipment Engineer Responsibilities: Develop and execute CQV testing documentation for utility systems within a sterile drug product manufacturing facility. Deliver on key project milestones, including safety, schedule adherence, and high-quality documentation/electronic records for assigned equipment and utilities. Ensure testing of utility systems complies with Good Manufacturing Practices (GMP), internal company policies, and EU/FDA regulatory standards. Oversee commissioning of non-GMP utility systems in line with project-specific standards. Manage deviations associated with assigned systems and equipment. Conduct risk assessments related to CQV activities; develop mitigation strategies to address potential qualification risks. Support Factory Acceptance Testing (FAT), and integrate outcomes into the overall qualification strategy for equipment, facilities, and utilities. Complete all required training in a timely manner to support site compliance metrics. Collaborate with site stakeholders, vendors, and contractors to ensure smooth project execution. Perform field inspections, FAT/SAT participation, and walkdowns to confirm proper installation and operation of systems. Required Competencies: Proven ability to independently execute CQV activities from initiation through to completion. Full lifecycle CQV project experience, including design, commissioning, qualification, and handover. Strong background in CQV for sterile drug product manufacturing environments, including utility systems with integrated automation. Hands-on experience with black utility systems (e.g., compressed air, plant steam, process waste, chilled water). Excellent technical documentation and execution skills, with a strong track record of meeting project timelines. Strong interpersonal and communication skills; ability to work effectively in cross-functional teams. Demonstrated ability to contribute within a matrixed team environment and manage multiple priorities simultaneously. Qualifications & Experience: Bachelor's degree in Engineering, Life Sciences, or a related technical discipline. Minimum of 5 years of CQV experience within the pharmaceutical or biotech industry, with a focus on utility systems and sterile manufacturing operations. The Next Step for you: Should this position be of interest to you please submit your CV to Barry O'Mahony from Next Generation Recruitment using the apply button. Next Generation are specialists in Supply Chain, Procurement, Engineering, Quality, Technical and Operation (permanent, contract and temporary) positions. Applications are in strict confidence. Next Generation will never share your data outside of our organisation without your prior written consent. Please read our Data Protection Policy on our website.