Sales Account Manager Recycling & IT Asset Disposition (Public Sector, Cork/Munster) Salary: €46,000€48,000 Field-Based | Munster Region | 10% Bonus | Permanent Are you a target-driven Sales Account Manager with experience in recycling, confidential shredding, environmental services or IT asset disposition? Our client, a progressive public sector organisation, is seeking a commercially focused sales professional to manage and grow B2B accounts across Cork and the wider Munster region. The full job description covers all associated skills, previous experience, and any qualifications that applicants are expected to have. Location: Primarily Cork (covering Clare, Cork, Kerry, Limerick, Tipperary & Waterford) Salary: €46,000€48,000 DOE Bonus: 10% on-target (up to 15% for exceeding targets) Expenses: Business mileage covered (no company car) Key Responsibilities Develop new business and manage existing B2B customer accounts across recycling, secure shredding and IT asset disposition services Achieve agreed sales targets and regional revenue KPIs Present service solutions to Facility Managers, Sustainability/CSR leads and IT departments Maintain accurate CRM records and report on leads, quotations, sales and pipeline activity Upsell the full range of environmental and secure data destruction services Work closely with operations and finance to ensure high-quality service delivery Essential Requirements Minimum 2 years B2B sales experience in a commercial, industrial or manufacturing environment - Relevant level 7 NFQ qualification Proven track record of achieving and exceeding sales targets Strong relationship management and negotiation skills Commercially aware, organised and self-motivated Proficient in MS Office and CRM systems Full clean driving licence and willingness to travel across Munster Desirable Experience in recycling, waste management, confidential shredding or ITAD Apply: Send your CV to Ben Higgins via the link below. xsokbrc Shortlisting may be based on the information provided. GHL Recruitment Connecting Talent with Opportunity Skills: Sales Targets B2B KPI Selling experience Executive Development ITAD Recycling Benefits: 23 days annual leave

Facilities Engineer About Astellas: At Astellas we are making treatments that matter to people. Find out more about this role by reading the information below, then apply to be considered. We are tackling the toughest health challenges putting the patient at the heart of every move we make. Our global vision for Patient Centricity is to support the development of innovative health solutions through a deep understanding of the patient experience. At Astellas, Patient Centricity isn't a buzzword - it's a guiding principle for action. We believe all staff have a role to play in creating a patient-centric culture and integrating an awareness of the patient into our everyday working practices, regardless of our role, team or division. We have developed ground-breaking, innovative medicines in immunology, oncology and urology. Our medicines are extending and saving the lives of cancer patients, making transplantation possible and improving the quality of life for those living with conditions where needs are often overlooked. We take a patient-focused approach, that allows us to convert brilliant early science into treatments and solutions that directly improve and save patients' lives. From lab to clinic to patient, we focus on the most promising science, empower the best talent to pursue it, and develop life-changing solutions alongside the best partners. The Opportunity: As a Facilities Engineer, you will be responsible for the operation, maintenance, regulatory compliance, procurement, and continuous improvement of all Facilities systems and equipment. You will oversee the implementation and adherence to the Energy Management System, ensuring that efficiency reviews of Facilities systems operations are conducted regularly. Additionally, you will play a key role in the efficient design review of all new equipment and processes, ensuring they align with best practices and sustainability goals. Key Responsibilities: Develop and implement operational/maintenance procedures to ensure best practices and regulatory compliance. Continuously improve Facilities and energy management systems for optimal operational and maintenance efficiency. Act as the SME owner of GMP & Non-GMP systems as required. Troubleshoot process-specific equipment and generate data/reports for Annual Product Quality Reviews and regulatory submissions. Lead or participate in cross-functional teams and support change control and commissioning/qualification activities. Maintain and improve the Energy Management System, ensuring compliance with energy policies, objectives, and relevant regulations. Essential Knowledge & Experience: Third-level qualification in Engineering or Science, or extensive proven experience in relevant fields, with experience in Pharmaceutical, Industrial, or Semiconductor processes. Strong knowledge of GMP, system validation, HVAC & Clean Systems (e.g., Purified Water, Pure Steam, WFI), and control systems; experience in Energy Management Systems is a plus. Familiarity with Health and Safety, Fire Systems, and Environmental Control Systems; excellent interpersonal, communication, and supervisory skills. Strong organizational, planning, problem-solving abilities, with a proactive approach, good documentation practices, and a flexible work attitude. Education: Third level qualification in an Engineering or Science discipline, or extensive related proven experience in the required areas. Additional information: This is a permanent full-time position. Position is based in Tralee, Ireland. This position requires you to be 100% on site/in the office. We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law. We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law. Beware of recruitment scams impersonating Astellas recruiters or representatives. Authentic communication will only originate from an official Astellas LinkedIn profile or a verified company email address. If you encounter a fake profile or anything suspicious, report it promptly to LinkedIn's support team through LinkedIn Help. #LI-Tralee #LI-Onsite To be considered for this role you will be redirected to and must complete the application process on our careers page. xsokbrc To start the process, click the Apply button below to Login/Register.

Watt Footprint is an Irish start up with global ambitions, already established as a leading force in the energy management in Ireland. Apply (by clicking the relevant button) after checking through all the related job information below. What makes Watt Footprint unique is our ability to combine our energy management software with hands-on engineering expertise to deliver a complete end-to-end solution for businesses of all sizes. From real-time energy insights and performance tracking through our platform, to feasibility assessments, energy audits, grant support, retrofit project delivery, and measured & verified savings, we help organisations achieve real, lasting reductions in energy cost and carbon impact. We are seeking a Partnership Manager to drive growth by developing and nurturing strong one-to-many relationships with key clients, partners, and influencers across our target sectors. This role is not transactional sales. Instead, you will build trusted, long-term partnerships that consistently generate opportunities for both our energy management software and our engineering services. You will act as a strategic point of contact, embedding Watt Footprint into our partners networks, client bases, and decision-making processes. This is a highly relationship-led role with significant face-to-face interaction. You will be confident engaging with senior stakeholders, presenting to groups, and representing Watt Footprint. Key Responsibilities Build and manage strategic partnerships that generate repeatable one-to-many opportunities for Watt Footprint Develop trusted, long-term relationships with partner organisations and senior decision-makers across key sectors Lead face-to-face engagement, representing Watt Footprint in client meetings, partner discussions, and on-site visits Deliver high-quality presentations, workshops, and platform demonstrations to groups of stakeholders, clearly communicating ROI, savings potential, and operational impact Drive partnership-led revenue growth across both our energy management software and engineering services Collaborate with sales, marketing, engineering, and product teams to convert partner introductions into successful projects and long-term client relationships and maximise cross sell. Maintain accurate tracking of partner activity, opportunities, and outcomes in our CRM. Required Skills & Experience Proven experience in partnership management, strategic account management, or senior B2B sales Strong track record of winning work through relationship-led, one-to-many partnerships rather than one-off transactional selling Confidence presenting in person to groups, leading meetings, and engaging senior stakeholders Excellent communication, negotiation, and stakeholder management skills Self-motivated, target-driven, and comfortable working in a remote-first start-up environment Full drivers licence and ability to travel to partner and client sites Experience in energy, sustainability, property, engineering, or infrastructure sectors is a strong advantage, but not essential Compensation & Benefits Competitive base salary plus commission linked to partnership-driven revenue Flexible working hours Laptop and remote working setup Professional development and progression opportunities Monthly team workshops and social events 23 days annual leave plus bank holidays and your birthday off Employer-funded health plan Employee Assistance Programme (EAP) Our Culture At Watt Footprint, we are united by our core values: Do It Right: We ensure a holistic view, doing it right from the start and setting our team and clients up for success. Adapt and Innovate: We challenge the norm and adapt to achieve the best results every time. Don't be an Activist, be an Actionist: We deliver real energy savings, taking action today for tomorrow's success. Open and Transparent: Effective communication and a transparent, open-book approach are key to our project delivery. xsokbrc Team Players: We build trust and support within the team, embracing collaboration. Benefits: Work From Home

Quality Assurance Validation Specialist About Astellas Astellas is a global life sciences company committed to turning innovative science into VALUE for patients. If you are considering sending an application, make sure to hit the apply button below after reading through the entire description. We provide transformative therapies in disease areas that include oncology, ophthalmology, urology, immunology and women's health. Through our research and development programs, we are pioneering new healthcare solutions for diseases with high unmet medical need. Learn . Are you driven to make a real difference in the lives of patients? We're seeking passionate individuals who thrive in dynamic environments, embrace new ideas, and aren't afraid to take intelligent risks. People who act with unwavering integrity and are deeply committed to making a tangible impact. Location and Working Environment This position is onsite in Killorglin, Ireland. Working Hours Part-Time: 0.6 FTE (Wednesday, Thursday, Friday). Purpose & Scope This role supports the development, improvement and control of GxP validation activities, ensuring compliance with site procedures and regulatory requirements. It includes QA governance, review and approval of validation documentation, and management of GxP change control processes. Role and Responsibilities Assessment of current practices to ensure compliance with GMP requirements. Familiarisation with developments and innovations in validation requirements. Review of procedures, reports and results for compliance. Review and approval of validation documents (URS, Validation Plans, OQ, PQ, Validation Reports). Review and approval of change controls and routine validations. Preparation of Periodic Review Reports. Participation in project teams ensuring validation meets internal procedures and GMP principles. Biannual Trend Review of GxP site change controls. QA management of GxP change control processes to maintain validated state. QA management of Computerised System Periodic Reviews. Generation of Product Quality Reviews for GxP change control activities. Required Qualifications BSc or equivalent academic qualification. Preferred Qualifications Knowledge of regulatory requirements for validation including aseptic processing, computerised systems, manufacturing processes, equipment and QC testing. Industrial or pharmaceutical experience is an advantage. What awaits you at Astellas? Global collaboration: Work within a connected global community dedicated to improving patient lives. Real-world patient impact: Contribute to life-changing therapies that make a difference worldwide. Relentless innovation: Join a company pushing scientific boundaries. A Culture of Growth: Thrive in a supportive environment that fosters development and progression. Our Organisational Values and Behaviours Impact Innovation Integrity One Astellas Accountability Courage Sense of Urgency Outcome Focus Benefits Careers | Astellas We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law. Beware of recruitment scams impersonating Astellas recruiters or representatives. Authentic communication will only originate from an official Astellas LinkedIn profile or a verified company email address. #LI-Killorglin #LI-Onsite #LI-LL1 To be considered for this role you will be redirected to and must complete the application process on our careers page. xsokbrc To start the process, click the Apply button below to Login/Register.

Kitchen/Cabinet Installer (Luxury kitchen & Cabinetry Company) Please ensure you read the below overview and requirements for this employment opportunity completely. Dublin €50-60k + Package Required for bespoke kitchen company seeking a highly skilled Cabinet Installers with exceptional finish carpentry expertise and a passion for precision craftsmanship. This role involves installing custom, bespoke, handcrafted made-to-measure kitchens in luxury residential homes. Responsibilities: • Install bespoke kitchens & cabinetry • Interpret detailed shop drawings and installation plans • Scribe, level, and align cabinetry for seamless, furniture-grade finishes • Protect high-value finishes and maintain immaculate job sites • Work closely with designers, project managers, and discerning clients Requirements: • 3+ years’ experience installing high-end or bespoke cabinetry • Advanced fitting/installation xsokbrc skills • Exceptional attention to detail and pride in workmanship • Valid driver’s license Excellent compensation aligned with experience and craftsmanship level To register your interest please forward CV to (url removed) or call (phone number removed) to discuss

Lyophilisation Lead Engineer About Astellas Astellas is a global life sciences company committed to turning innovative science into VALUE for patients. Find out if this opportunity is a good fit by reading all of the information that follows below. We provide transformative therapies in disease areas that include oncology, ophthalmology, urology, immunology and women's health. Through our research and development programs, we are pioneering new healthcare solutions for diseases with high unmet medical need. Learn . Are you driven to make a real difference in the lives of patients? We're seeking passionate individuals who thrive in dynamic environments, embrace new ideas, and aren't afraid to take intelligent risks. People who act with unwavering integrity and are deeply committed to making a tangible impact. Location and Working Environment This position is 100% onsite in Tralee, Ireland. Purpose & Scope Provide technical support to lyophilisation operations, engineering, and control systems to ensure efficient, compliant operations. Ensure GMP compliance and data integrity of computerised systems. Lead deviations, investigations, CAPAs, and root cause analysis. Drive continuous improvement using Lean Six Sigma. Manage projects, technology transfer, commissioning, and cross-functional collaboration. Apply strong analytical and automation/SCADA/PAT expertise. Role and Responsibilities Support lyophilisation operations and ensure achievement of production and project schedules. Maintain compliance with cGMP, ISO 14001, EMAS, Health & Safety, and Environmental legislation. Train and develop staff; maintain SOPs and documentation. Support Operational Excellence initiatives and promote strong teamwork and safety culture. Required Qualifications Bachelor's or Master's degree in Chemical Engineering, Pharmaceutical Sciences, Bioprocess Engineering, Biotechnology, or related field, or extensive relevant experience. Preferred Qualifications Experience in lyophilisation process development or operations (e.g., Lyomax). Expertise in aseptic vial lyophilisation, CIP/SIP/FIT, process instrumentation, control systems, qualification, and validation. Strong organisational, interpersonal, verbal, and written communication skills. Ability to work independently or as part of a team. What awaits you at Astellas? Global collaboration. Real-world patient impact. Relentless innovation. A culture of growth. Our Organizational Values and Behaviors Impact Innovation Integrity One Astellas Accountability Courage Sense of Urgency Outcome Focus Benefits Careers | Astellas We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law. Beware of recruitment scams impersonating Astellas recruiters or representatives. Authentic communication will only originate from an official Astellas LinkedIn profile or a verified company email address. If you encounter anything suspicious, report it promptly to LinkedIn's support team through LinkedIn Help. #JU-1 #LI-Onsite #LI-Tralee To be considered for this role you will be redirected to and must complete the application process on our careers page. xsokbrc To start the process, click the Apply button below to Login/Register.

Validation Lead About Astellas Astellas is a global life sciences company committed to turning innovative science into VALUE for patients. The following information aims to provide potential candidates with a better understanding of the requirements for this role. We provide transformative therapies in disease areas that include oncology, ophthalmology, urology, immunology and women's health. Through our research and development programs, we are pioneering new healthcare solutions for diseases with high unmet medical need. Learn . Are you driven to make a real difference in the lives of patients? We're seeking passionate individuals who thrive in dynamic environments, embrace new ideas, and aren't afraid to take intelligent risks. People who act with unwavering integrity and are deeply committed to making a tangible impact. Location and Working Environment This position is 100% onsite in Tralee, Ireland. Purpose & Scope Lead the daily operations of the Validation function, managing Validation Engineers (staff and outsourced providers), coordinating activities, and improving operational efficiency. Ensure facilities, utilities, equipment, computerized systems, manufacturing processes, cleaning procedures, analytical methods, and aseptic operations perform as intended and reliably produce safe, effective, and compliant biopharmaceutical products. Provide strategic leadership across the validation lifecycle-planning, execution, review, approval, and maintenance-aligned with GMP, data integrity principles, and risk-based methodologies. Own the Site Validation Master Plan (VMP), champion cross-functional governance, and drive continuous improvement to maintain a validated state. Role and Responsibilities Lead and develop the Validation team; foster an engaged, psychologically safe, high-performance culture aligned with Astellas values. Ensure stable supply and delivery of departmental objectives; resolve issues, prioritise effectively, and drive continuous improvement via ambitious KPIs. Maintain compliance with GMP, GDP, environmental, safety, and governance requirements; ensure audit readiness and robust data integrity. Contribute to site and global strategy; deliver strategic projects on time and within budget while anticipating future trends and skill needs. Lead implementation of new products, technologies, systems, and procedures; ensure compliant change management and effective knowledge transfer. Build strong cross-functional and global partnerships; support business continuity, mitigate risks, and deputise for site leaders as required. Required Qualifications Bachelor's degree (or equivalent) in an Engineering or Scientific discipline, or proven relevant in-depth experience. Preferred Qualifications Extensive experience in a similar role with strong technical competence and validation leadership capability (cGMP start-up experience advantageous). Proven ability to progress complex technical projects, support commissioning/maintenance of cGMP manufacturing, and manage multiple priorities. Excellent organisational, interpersonal, verbal, and written communication skills; able to work independently and collaboratively; open to new ideas. What awaits you at Astellas? Global collaboration: Become part of a connected global business of like-minded life science leaders, all dedicated to improving patients' lives. Real-world patient impact: Contribute to transformative therapies that reach patients around the world. Relentless innovation: Join a company at the forefront of scientific breakthroughs. A culture of growth: Thrive in a supportive environment that champions your development. Our Organizational Values and Behaviors Impact Innovation Integrity One Astellas Accountability Courage Sense of Urgency Outcome Focus Benefits Learn more: We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law. Beware of recruitment scams impersonating Astellas recruiters or representatives. Authentic communication will only originate from an official Astellas LinkedIn profile or a verified company email address. If you encounter a fake profile or anything suspicious, report it promptly to LinkedIn's support team through LinkedIn Help. #LI-Tralee #LI-Onsite #LI-ND1 To be considered for this role you will be redirected to and must complete the application process on our careers page. xsokbrc To start the process, click the Apply button below to Login/Register.

Site Engineer – (Developer/contractor) All potential candidates should read through the following details of this job with care before making an application. Dublin 15 €55–65K + Bonus + Allowance Required for reputable contractor who are undertaking a 9-storey residential project. Clear pathway to Senior Engineer. What You’ll Do • Set out control points, datums & gridlines for Groundwork, Concrete frame, Brickwork • setting-out / checking subcontractor setting-ou • inspecting quality of the works • raising RFI’s / design information review • checking & coordination Reporting to the Senior Engineer What You Bring • Degree/Diploma in Engineering / Surveying / Construction xsokbrc • 3+ years’ experience (main contractor ideal) Clear progression on offer. To register your interest please forward CV to (url removed) or call (phone number removed) to discuss

Siemens Healthineers is searching for an experienced Quality and Regulatory professional for the role of Head of Quality & Regulatory Are you the right applicant for this opportunity Find out by reading through the role overview below. - GB&I. This individual will be part of our leadership team and will be responsible for leading all aspects of our Quality and Regulatory approaches. This will ensure that our products and services meet or exceed our customers' requirements while supporting our business objectives. The Head of Quality & Regulatory - GB&I's responsibilities will include regulatory compliance so that our products and services are able to be placed on the market. This will require working closely with all departments and Business Lines to ensure that the requirements of our markets are clearly understood. Our GB&I zone continues to see emerging requirements that are unique, challenging and which need to be understood and articulated across the whole of Healthineers globally. BREXIT, the Social Value Model (SVM), Environmental, Social and Governance (ESG), Value Based Procurement together with Digital Security are examples of changes that will continually evolve, and which will require Siemens Healthineers to continually improve to remain competitive. These emerging requirements will need to be supported by completion of responses to tender specifications around topics such as cyber security, social responsibility and sustainability. This will require the role holder to collaborate with many departments at all levels within zone and globally. The ideal candidate will: Have experience of leading and guiding a team of experts within the complex regulatory and legislative environment of the UK and Ireland. Have a strong understanding of regulatory procedures and standards, such as ISO 9001, European Medical Device Regulations (EU MDR), UK MDR together with knowledge of our key regulators which will include the MHRA and the HPRA. Be required to engage directly with Government Departments, Regulators, Industry Bodies, Certification Bodies, Customers and Suppliers which will require knowledge of local, national, and international requirements. Head of Quality & Regulatory - GB&I Mission The mission for you as the Head of Quality & Regulatory - GB&I will be to represent the Siemens Healthineers Zone in the SHS QT community (QM and RA) and related activities. You'll have the responsibility to identify and address zone-wide synergies and operational improvements. In addition, you'll act as QT-partner for the Zone Leadership Team and manage QT relevant escalations as needed. The role reports directly and functionally to the Zone Head (Executive VP, MD for Siemens Healthineers GB&I). You'll be responsible for implementing the requirements of Directive 1_D_79 and the SHS requirements (such as but not limited to QRs and ARTDs marked as Directives) in your area of responsibility, as far as applicable. Role Purpose You'll have Zone-wide authority for all applicable SHS QT aspects in coordination with the SHS Zone Head and SHS QT.In this role you'll lead the development and execution of Siemens Healthineers' Quality and Regulatory in Great Britain and Ireland to ensure compliance with internal and external regulations and support customer requirements. This position is critical to lead our approaches for our formal management system certifications and for delivering all statutory reporting. Key Responsibilities Lead the GB&I QT Team to deliver regulatory compliance to statutory requirements by national regulators. Significant regulations include UK MDR 2002 (MHRA) and regulations related to Product Related Environmental Protection (PREP; Environment Agency and the Health and Safety Executive). Management System Certifications. Directly maintain the following management systems and certificates through management of subject matter experts: - ISO9001 Quality - ISO22301Business Continuity CE+Cyber Essentials certification Provide support to the following management systems and certificates through management and engagement of QT subject matter experts: - ISO14001Environment (PREP) - ISO27001 Information Security (CYSO) Technical Regulations and Standards Manage our compliance to technical standards that are applicable to our products and services. This includes UK specific requirements, including clinical safety requirements together with product related technical standards. NCC (non-conformance cost) Manage our overall approaches for reporting NCCs. To include identification of root causes and subsequent areas for improvement using Healthineers Performance System methodologies (HPS). Required Skills and Qualifications Strong communication skills with the ability to influence at all levels. Strong analytical skills to be able to identify key areas in order to maximise value add and ensuring effective management of risk. Leadership experience and the ability to coach and mentor diverse teams Experience of working in an international environment. Proven experience of working with external stakeholders including customers, suppliers, certification bodies and regulators. The ideal candidate will have extensive experience of managing formal certified management systems and be an accomplished auditor. The ideal candidate will have Project Management experience and knowledge of improvement techniques (LEAN, HPS, Six Sigma). Qualifications or proven extensive experience in Auditing, Business Continuity, Environmental Management, Information/Cyber Security, Quality Management and Regulatory Affairs. Core Benefits: Competitive base salary Bonus scheme 10% matched pension contributions BUPA Private Medical 26 days holiday (with option to buy/sell up to 5) plus statutory Life Assurance Share save scheme A range of additional salary sacrifice benefits including EV car schemes, global travel insurance, dental plans and critical illness cover Significant work from home aspect - expected to be WFH circa 80-90% of the time Who we are: We are a team of more than 71,000 highly dedicated Healthineers in more than 70 countries. As a leader in medical technology, we constantly push the boundaries to create better outcomes and experiences for patients, no matter where they live or what health issues they are facing. Our portfolio is crucial for clinical decision-making and treatment pathways. How we work: When you join Siemens Healthineers, you become one in a global team of scientists, clinicians, developers, researchers, professionals, and skilled specialists, who believe in each individual's potential to contribute with diverse ideas. We are from different backgrounds, cultures, religions, political and/or sexual orientations, and work together, to fight the world's most threatening diseases and enable access to care, united by one purpose: to pioneer breakthroughs in healthcare. For everyone. Everywhere. Sustainably. As an equal opportunity employer, we welcome applications from individuals with disabilities. Siemens Healthineers are proud to be a Disability Confident Committed employer. If you require any adjustments at any stage of the recruitment process, please let us know. We care about your data privacy and take compliance with GDPR as well as other data protection legislation seriously. For this reason, we ask you not to send us your CV or resume by email. Please create a profile within our talent community and subscribe to personalized job alert that will keep you posted about new opportunities. To all recruitment agencies: Siemens Healthineers' recruitment is internally managed, with external support permitted only when a qualified supplier has established a formal contract with us. Unsolicited candidate submissions and referrals, absent a current supplier contract, do not establish consent and are ineligible for fees. We delete and destroy unsolicited information, thus, would recommend you refrain from any such practices. Your adherence to our policies is appreciated. To be considered for this role you will be redirected to and must complete the application process on our careers page. xsokbrc To start the process, click the Apply button below to Login/Register.

Role is based in Denmark with rotations to Ireland GerTEK is an engineering consultancy company specialising in project management, talent solutions, and commissioning, qualification, and validation (CQV) services. Below, you will find a complete breakdown of everything required of potential candidates, as well as how to apply Good luck. We partner with many of the world's largest life science and technology companies, who entrust us to deliver their most strategic and important projects. We are seeking highly motivated and experienced QA/QC Inspectors in the electrical, mechanical and CSA fields to join our team for data centre construction projects. The ideal candidates will ensure all construction activities meet project specifications and quality standards. Responsibilities: Perform inspections of structural/mechanical/electrical, and other installations. Document and report any non-conformances. Verify corrective actions. Review and approve contractor quality documentation. Conduct material testing and inspections. Collaborate with project teams to ensure quality compliance. Qualifications: Proven experience as a QA/QC Inspector in the construction industry or similar Strong understanding of relevant codes and standards. Excellent documentation and communication skills. xsokbrc #Gertek To start the process click the Continue to Application or Login/Register to apply button below.