Overview of salaries statistics of the profession "Quality Engineer in Connacht"
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Overview of salaries statistics of the profession "Quality Engineer in Connacht"
2 759 £ Average monthly salary
Average salary in the last 12 months: "Quality Engineer in Connacht"
The bar chart shows the change in the level of average salary of the profession Quality Engineer in Connacht.
Similar vacancies rating by salary in Connacht
Among similar professions in Connacht the highest-paid are considered to be Automation Engineer. According to our website the average salary is 6447 GBP. In the second place is Equipment Engineer with a salary 4518 GBP, and the third - Forensic Engineer with a salary 4518 GBP.
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Design Assurance Engineer
A leading Medical Device client in Sligo is hiring a Design Assurance Engineer.About the Job:Assist with the development of quality evaluation and control plans and protocols for processing materials into finished products;Issue of Product paperwork/lot records to manufacture and also review and release of same and compile COA/COCSupport QMS as Quality Coordinator in the investigation into non-conformances, participate in root cause analysis and with disposition and or agree corrective and preventative action (CAPA) recommendations related to manufactured products including review and approval of deviations and customer complaints etc.;Quality review of responsible area validation documentation of Design & Development Documents;Participating in design reviews and the compilation of associated documentation;Co-ordination of internal testing reports, biocompatibility testing reports & technical file development, sterilization qualificationGenerate & Maintenance of Product Design Files;Routinely provides design assurance guidance & direction to project manager & design engineers for the duration of a project development;Work closely with product development engineering team and the client to establish design specifications and product requirements;Support execution of Design Verification and Validation planning;Ensure DHF content completion, and regulatory & standards compliance; collaboratively communicating & resolving gaps;About you:Minimum Degree in a Science or Engineering discipline.3-5 Years’ experience working in a medical device environment in a Design Assurance Engineering role, (preferably with involvement in product design and R&D).Strong knowledge of ISO 13485, FDA regulations 21CFR 820.Internal/external auditing experience would be an advantage.Validation experience including Sterilization, process and packaging validations would be beneficialKnowledge of Medical Device manufacturing environment including cGMP would be an advantage.Understand general principles of ISO 14971.For more on the role call Nigel on 087 3618142 or send your CV for consideration.
, Galway, Republic of
Title: Quality EngineerLocation: Spiddal, County GalwayBenefits: Opportunity to progress your career in a company who promotes from within, good salary, pension, healthcare and yearly bonus.Role:The position requires an experienced and proven candidate with a background in Quality and Regulatory control of Medical Devices. The successful candidate will work as part of a team to maintain high quality/performance standards across the companyResponsibilities:Develop and maintain documentation in compliance with FDA , ISO, MDD requirementsActively participate in the Documentation control processReview / Approve / Release final product documentationInitiate / Approve Non-Conformance Reports & Lead Root Cause analysis investigationsParticipate / Lead Risk Analysis initiatives e.g. FMEAInitiate / Approve ReworksInitiate / Support implementation of effective Corrective / Preventive ActionsSupport the Environmental monitoring processSupport activities associated with SterilizationAct as the QA representative for Supplier Quality management activitiesRepresent QA as part of the Material Review BoardAct as the QA representative on Design Services Projects / ChangesInitiate / Approve Validation protocols and reports (IQ, OQ, PQ)Initiate / Approve Engineering Change noticesProcess Customer Complaints and manage customer repliesSupport Notified Body / Regulatory Agency / Customer AuditsPerform Internal and Supplier AuditsCollate and trend Key performance indicator data on a monthly basis Role RequirementsDegree in manufacturing engineering, quality engineering, life science or related field and a minimum of 3 yrs. experience of working as a Quality Engineer within the Medical Device Industry.Candidate must be highly motivated with excellent communication skills and proven ability to work as part of a team.Experience of using Lean Manufacturing Tools and Techniques an advantageWould you be interested in applying? If so forward an up to date CV or contact me on the details provided to discuss further.Look forward to hearing from you.To find out more about Real please visit Real Staffing, a trading division of SThree Partnership LLP is acting as an Employment Agency in relation to this vacancy| Registered office | 1st Floor, 75 King William Street, London, EC4N 7BE, United Kingdom | Partnership Number | OC(phone number removed) England and Wales
, Galway, Republic of
Quality EngineerCommutable from: Galway, Limerick and ClarePosition Reports To: Quality ManagerProvide inspection and root cause analysis support for components and products subject to complaints or internal investigation. Chair 8D meetings to identify root cause analysis determining with a cross functional team actions to resolve the complaint or issue. Supported by the Senior Quality Engineer (SQE) and or Quality Manager (QM). Expect to be involved in Internal Auditing, planning, scheduling and some co-ordination.Duties & ResponsibilitiesSupport and drive the Company Quality PolicyProcess Development - Output Auditable to IATF16949 or other standards as requiredDevelop Process Steps through the creation/updating and maintenance of PFMEAsFlow identified characteristics through to Work Instructions and Control Plans, originate documentation such as control plans and inspection sheets,Support internal Audit Procedures, planning and executionSupport maintaining quality system for IATF 16949Drive Corrective Actions through the 8D process where issues occur or KPIs are not met o Develop to chairing and co-ordinating meetingsCoordinate investigations on defective partsParticipates in the development and creation of failure mode effect analysis (FMEA) including Design (DFMEA) and Process (PFMEA)Understand the PPAP Process and demonstrated capability to pull necessary documentation together to supply the end customer.Ensure your area is properly organized to maintain 5S and to identify opportunities for improvementPromote the culture of quality and operator responsibility for workmanship and qualityDevelopment of processes auditable to IATF16949Ensure the control and disposition of non-conforming product in your designated areaCoordinating or obtaining engineering concessions for non-conforming product where acceptableDocument work instructions, facilitate CI improvementsQualifications & Experience:A relevant 3rd level qualification and a minimum 2 years of Quality experienceMicrosoft Windows-Office and EXCEL applicationsKnowledge of ISO9001, IATF16949Team Dynamics and Inter-personal skillsProblem Solving using appropriate quality tools, 5 Why's, Ishikawa, Is/Is notBasic Statistical Process Control and Statistical FundamentalsUnderstand Geometric Dimensioning and Tolerances and measurement methodsBlue Print reading and interpretationMust possess excellent communications, teamwork, and leadership / conflict management skills.Ability to interface with customers, suppliers and employees, problem solve and drive solutions to meet their requirements..Maintains a high level of professionalism, integrity and trust. Able to handle sensitive information and maintain confidentialityMust have a 'can do' attitude with a willingness to undertake any task requiredFor more information on this role in Galway please contact Mark Wilson on (phone number removed) or Check out all our open jobs on our HERO Recruitment website
SAP Ireland - Support Engineer - ERP4SME Development Support
SAP, Galway, IE, HWP
What we offerOur company culture is focused on helping our employees enable innovation by building breakthroughs together. How? We focus every day on building the foundation for tomorrow and creating a workplace that embraces differences, values flexibility, and is aligned to our purpose-driven and future-focused work. We offer a highly collaborative, caring team environment with a strong focus on learning and development, recognition for your individual contributions, and a variety of benefit options for you to choose from. Apply now!Do you demand the best from your professional career? Are you inspired by excellence? At SAP, you will have the power to make a real impact. SAP is the Global Market Leader in Enterprise Application Software and the Top Cloud Vendor and Leading Mobility Vendor. With offices and labs located worldwide SAP serves over 320,000 customers in 190 countries, including 87% of the Global Fortune 500 and 98% of the 100 most valued brands. 74% of the world’s transaction revenue touches an SAP system.PURPOSE AND OBJECTIVESSAP Business ByDesign is SAP’s comprehensive cloud ERP solution for fast-growing, mid-market businesses. It delivers pre-built processes for everything from finance and sales to product management and purchasing on a single, unified solution. The ERP4SME Development Support team provide L2/L3 Support on the following application areas of ByDesign currently: Financials (FIN) / Customer Relationship Management (CRM) / Human Capital Management (HCM) / Supply Chain Management (SCM) and Supplier Relationship Management (SRM). Core responsibilities include providing thorough Root Cause Analysis and data corrections for complex customer issues at L2/L3 level for Business ByDesign. The team are currently recruiting for open positions in the FIN, CRM and SCM areas. Close collaboration with internal & external stakeholders as well as the Core Development Teams is a critical requirement to execute this responsibility.EXPECTATIONS AND TASKS• The candidate must ramp up quickly on technical aspects and understand functional domain of Financials, Customer Relationship Management or Supply Chain Management. • Handle L2/L3 customer incidents independently on time and with quality• Intensive debugging of issues and co-ordination across many teams• Communication with customers and partners to identify, understand and solve product-specific problems• Develop strong working relationships with cross-functional teams within the ERP4SME Development core team• Follow SAP product standards applicable for application development following agile methodologiesEDUCATION AND QUALIFICATIONS / SKILLS AND COMPETENCIES• Bachelor’s Degree in Computer Science, IT, or similar required• Understanding of Object Orientated Programming Principles• Strong analytical and problem-solving skills• Strong ability to capture a complete and accurate problem/symptom description of reported issues• Knowledge of relational databases is an advantage • Knowledge and experience of ABAP/OO ABAP programming language • Excellent communication skills • Self-motivated, self-driven, curious, open minded, resourceful and flexible with the ability to learn quicklyWORK EXPERIENCE• 3-4 years’ experience as a Support/Development Engineer• Experience of Object-Oriented Programming is a distinct advantage • Experience of problem solving and debugging code is required• Experience in agile software development is an advantage• SAP Application knowledge (FIN, CRM or SCM) is a distinct advantageWe are SAPSAP innovations help more than 400,000 customers worldwide work together more efficiently and use business insight more effectively. Originally known for leadership in enterprise resource planning (ERP) software, SAP has evolved to become a market leader in end-to-end business application software and related services for database, analytics, intelligent technologies, and experience management. As a cloud company with 200 million users and more than 100,000 employees worldwide, we are purpose-driven and future-focused, with a highly collaborative team ethic and commitment to personal development. Whether connecting global industries, people, or platforms, we help ensure every challenge gets the solution it deserves. At SAP, we build breakthroughs, together.Our inclusion promise SAP’s culture of inclusion, focus on health and well-being, and flexible working models help ensure that everyone – regardless of background – feels included and can run at their best. At SAP, we believe we are made stronger by the unique capabilities and qualities that each person brings to our company, and we invest in our employees to inspire confidence and help everyone realize their full potential. We ultimately believe in unleashing all talent and creating a better and more equitable world.SAP is proud to be an equal opportunity workplace and is an affirmative action employer. We are committed to the values of Equal Employment Opportunity and provide accessibility accommodations to applicants with physical and/or mental disabilities. If you are interested in applying for employment with SAP and are in need of accommodation or special assistance to navigate our website or to complete your application, please send an e-mail with your request to Recruiting Operations Team: Americas: Careers.NorthAmerica@sap.com or Careers.LatinAmerica@sap.com, APJ: Careers.APJ@sap.com, EMEA: Careers@sap.com.EOE AA M/F/Vet/Disability:Qualified applicants will receive consideration for employment without regard to their age, race, religion, national origin, ethnicity, age, gender (including pregnancy, childbirth, et al), sexual orientation, gender identity or expression, protected veteran status, or disability. Requisition ID:292355 | Work Area: Customer Service and Support | Expected Travel: 0 - 10% | Career Status: Professional | Employment Type: Regular Full Time | Additional Locations:
Senior R&D Engineer
Morgan McKinley, Galway, ie
A fantastic opportunity has just become available to join a forward-thinking Medical Device company as a Senior R&D Engineer Due to the continued growth and success of a world-renowned medical device company based in Galway, I'm looking to speak to experienced R&D Engineers looking to move into a new and exciting challenge. The successful candidate will be responsible for the design and development of next-generation minimally invasive medical devices.Key ResponsibilitiesLead engineering design, development and support of new and current heart valve products.Create/develop technical capabilities and expertise related to the design and testing of heart valve technology.Develop fatigue test methods and characterisation techniques to evaluate performance of valve prototypes.Coordinate with outside consultants and clinicians to ensure testing and analyses required to fully qualify and verify device designs are appropriately representative of expected use conditions.Work closely with team members and internal partners in Regulatory, Quality, Manufacturing, Marketing and other departments to deliver project objectives.Provide clear and regular technical direction to personnel assigned to a project.Maintain technical knowledge current with advancing technology related to cardiac valve prostheses and associated technologies in addition to knowledge of competitive technologies.Identify, evaluate, manage, and provide guidance to suppliers, including establishing tolerances and defining acceptance criteria for suppliers related to materials, manufacturing processes and design.Support manufacturing and quality groups for improvements to existing products in the areas of quality enhancement, product cost and product performance.Prepare or direct the preparation of oral and written reports of current status, progress and status of total project, as required by the customer, project or department Management.QualificationsA bachelor's degree or Post-Graduate degree in Engineering or related discipline is required.Position requires a minimum of 6 + years engineering experience to include valve development, specification development, and prototyping. Prior experience involving catheter-based technologies is advantageous.Experience in leading technical projectsRequired Skills:Experience in the design and development of valve prostheses and associated processes are required.Experience with medical device testing of vascular prostheses and/or catheter delivery systems.Understanding and extensive application of technical principles, theories, and design concepts in implantable productsGood understanding of the Human Anatomy is strongly desiredIn depth understanding of fluid mechanics and computational fluid dynamics particle image velocimetry is strongly desired.Morgan McKinley is acting as an Employment Agency and references to pay rates are indicative.BY APPLYING FOR THIS ROLE YOU ARE AGREEING TO OUR TERMS OF SERVICE WHICH TOGETHER WITH OUR PRIVACY STATEMENT GOVERN YOUR USE OF MORGAN MCKINLEY SERVICES.
, Galway, County Galway, Republic of
OverviewA well qualified, experienced and proven candidate with a background in Quality and Regulatory control of Medical Devices is required for a permanent role in a thriving community within the West of Ireland. The successful candidate will work as part of a team to maintain high quality/performance standards across the company.Role RequirementsA degree in manufacturing engineering, quality engineering, life science or related field and a minimum of 3 yrs. experience of working as a Quality Engineer within the Medical Device Industry.Candidate must be highly motivated with excellent communication skills and proven ability to work as part of a team.Experience of using Lean Manufacturing Tools and Techniques an advantageQuality Certification and Lead Auditor Certification while not mandatory would be an advantage.Reporting to the Snr QE Lead, the position will be challenging and will require an ability to work autonomouslyRoles & ResponsibilitiesThe Quality Engineer shall: * Develop and maintain documentation in compliance with FDA , ISO, MDD requirements * Actively participate in the Documentation control process * Review / Approve / Release final product documentation * Initiate / Approve Non-Conformance Reports & Lead Root Cause analysis investigations * Participate / Lead Risk Analysis initiatives e.g. FMEA * Initiate / Approve Reworks * Initiate / Support implementation of effective Corrective / Preventive Actions * Support the Environmental monitoring process * Support activities associated with Sterilization * Act as the QA representative for Supplier Quality management activities * Represent QA as part of the Material Review Board * Act as the QA representative on Design Services Projects / Changes * Initiate / Approve Validation protocols and reports (IQ, OQ, PQ) * Initiate / Approve Engineering Change notices * Process Customer Complaints and manage customer replies * Support Notified Body / Regulatory Agency / Customer Audits * Perform Internal and Supplier Audits * Collate and trend Key performance indicator data on a monthly basis * Actively participate in Management Review & Compliance meetings * Performs other related duties, as assigned
Senior Supplier Quality Engineer
, Galway, Republic of
Title Senior Supplier Quality Engineer Duration: 12 months FTC Location: Galway Start Date: ASAP Summary Our client, a medical device company in Galway is currently looking to recruit a Senior Supplier Quality Engineer for their site. The Pre-Market Supplier Quality team are directly involved in driving component qualification through effective partnership with external suppliers and internal design and development teams.A DAY IN THE LIFE OF:Partner with Technical Sourcing to locate, evaluate, and approve new potential component/material suppliers that balance business, quality, and technical requirements.Drive supplier requirements by collaborating with Development Engineering and other cross-functional partners to clarify design intent, identify critical features, and assess feature impact level. Partner with suppliers to ensure components are designed for reliability, manufacturability, and cost.Perform process and component/material development work with suppliers to deliver highly capable components/materials. Applies principles of chemistry, physics and material behaviours in the development of supplier processes. Define component qualification strategy, partner with suppliers to develop qualification plan, report performance, and demonstrate release readiness. Support project deliverables, supply risk reduction, yield improvement and cost reduction activities during developmentWork to develop proper inspection tooling and test methods for new components to ensure supplier parts meet specification requirements. Perform statistical data analysis to determine tool and part/process performance. Evaluate Supplier capabilities for mechanical measurement via Gage R&R studies. Ensure appropriate acceptance activities are in place prior to commercialization.Develop and deliver the Product Acceptance Sampling Strategy, Approved Supplier List coordination, Supplier Owned Quality deployment, and Control Plans for new products.Define Receiving Inspection requirements as required and associated test method validation for all internal Medtronic Test MethodsLead issue resolution of complex problems as they relate to supplied components and materials. Ensure corrective and preventive measures meet acceptable standards of robustness and effectiveness.Plan, execute, and communicate own work and educating others on work products. Provide regular, timely communication to manager and project team regarding status of assigned activities.KEY SKILLS & EXPERIENCEThird Level - Level 8 Degree in Science, Engineering or related discipline and 5 years' experience in component/materials development, reliability, manufacturing or processing/component fabricationApplied knowledge of DOE, SPC, FMEA, Gage R&R, Basic StatisticsDemonstrated technical writing skills Proficient in MS Office - MS Project focus Experienced with inspection equipment and material testing processesCapable of coordinating cross functionally with groups such as Design Engineering, Sourcing, Project Management, Operations, Commodity management, and Design Assurance to resolve issues and provide status of assigned activitiesDesired/Preferred QualificationsMasters in Materials Science or EngineeringSix Sigma green belt or black belt certified Design for Reliability and Manufacturability knowledgeExcellent communication skills; both written and oral, internal and external to the company. High level of statistics and DOE knowledgeDemonstrated success in process improvement and controlUnderstanding of material properties and how they can be impacted by Supplier processes.Advanced knowledge of measurement systems and knowledge of Supplier processes (EDM, CNC, Laser, Chemical, Plasma, Stamping, Milling, Polymer Processing, Moulding, Extrusion, etc.); advantages/disadvantage of various manufacturing methods for different commodity types, manufacturability, assembly, and process control.Experience with ANSI Y14.5M requirements (GDT)Experience with working with Contract ManufacturesProduct and Clinical Understanding; knowledge of vascular anatomy, physiology, primary disease states and Cardiovascular products For further information on this role please contact Shane Connolly on (phone number removed) or Check out all our open jobs on our HERO Recruitment website
Process Development Engineer Contract
, Galway, Republic of
Process Development Engineer Contract Our client, a leading medical device company located in Galway is recruiting for a contracting role. This PD Engineer role is commutable from Clare and Mayo. You will work closely with R&D and Manufacturing in the development of robust, capable, cost effective & safe manufacturing processes and products. And develop equipment, materials and products and supports efficient and effective transfer of new products & processes into commercial production.Key ResponsibilitiesDemonstrates strong technical expertise on process/product technologies to support selection, design, optimisation, validation and troubleshooting of, and can mentor engineers and technicians in problem resolution on, those technologies.Liaises with Equipment Engineering or external equipment/tooling or material vendors in the selection, design & development of new (or upgrades to existing) equipment, tooling and materials.Demonstrates strong knowledge of DFSS/DMAIC tools and applies these tools in the characterization, optimization and troubleshooting of process equipment and technology performance.Leads the development and execution of experimentation and testing to enable characterisation, optimization and troubleshooting of key processes and equipment.Co-ordinates the introduction of new processes, equipment and materials including installation, calibration, EHS assessment debug, and all associated process and quality system documentation requirements including technical and process work instructions.Demonstrates strong knowledge and application of Lean methodologies, and process improvement tools in identification and elimination of "waste" process steps and development of efficient, cost effective equipment and processes.Demonstrates strong knowledge and application of Process and equipment validation techniques, PFMEA's, and associated regulatory requirements and applies this knowledge in the efficient & timely validation of equipment and processes.Completes or leads the writing and release of process validation documentation including FMEA's, Validation Plans, protocols and reports.Co-ordinates execution and documentation of validation builds, co-ordinates testing of validation units and the compilation, analysis and reporting of the validation results.Demonstrates a primary commitment to patient safety and product quality.Understands and complies with all the regulations governing the quality systems.In all actions, demonstrates a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures.Establishes and promotes a work environment that supports the Quality Policy and Quality System.The candidate must:Be a developing professional. Working knowledge and application of business and technical concepts, procedures and practices. General knowledge of industry practices, techniques, and standards. General understanding of business unit/group function. Exercises judgment when interpreting company policies and procedures to resolve a variety of issues.Develop solutions to a variety of problems of moderate scope and complexity where analysis of situations or data requires a review of identifiable factors. Exercise judgment to determine appropriate action. Has knowledge of alternatives and an understanding of their impact on the business or technological environment.Plans, organizes, and prioritizes own daily work routine to meet established schedule.Works under general direction regarding the progress of projects and special assignments. May seek guidance in resolving problems, interpreting established policies, procedures and practices. Work is reviewed for soundness of judgment.Cultivates a wide range of internal business relationships and begins to develop an external network of resources to facilitate completion of tasks. May lead a project team of small to moderate scope. Influence exerted at peer level and occasionally at first levels of management.Contributes to the completion of departmental projects and goals. Errors in judgment, poor recommendations, or failure to achieve results would normally require a moderate expenditure of resources to rectify.Engages with internal company and external contacts. Represents organization on specific projects. Uses diplomacy and tact in interactions and problem solving. Provides guidance to less experienced staff.For further information on this contract PD Engineer role in Galway please contact Deirdre Finnerty on (phone number removed)/ Check out all our open jobs on our HERO Recruitment website
, Galway, Republic of
Job Title: Quality Engineer Duration: 12 months initial FTC Location: Galway Responsible for assuring products conform to established requirements and standards through appropriate audit, inspection, and test activities. The creation / development of procedures, manufacturing workflows, validation of required processes, developing inspection control plans, analysing quality trend data and taking appropriate action; supporting production on all quality related issues; investigating customer complaints; and ensuring an effective and robust quality system which complies with all relevant regulatory requirements.Key Responsibilities:*Formulates procedures, specifications, and standards for Client products and processes.Provides leadership for quality engineering projects from concept through design, implementation, testing, documentation, support, and maintenance.Develops and implements corrective/preventative action plans.Collects and analyzes data for gauge and product evaluation.Develop and maintain an effective and robust quality system which complies with all relevant regulatory requirements.Ensure all validation activity is effective and documented in a compliant manner.Complete in-depth investigations into, product non-conformance's, customer complaints and implement corrective and preventative actions, as appropriate.Identifies critical personnel, gauges, procedures, and materials needed for the completion of new products.Ensures that suppliers have necessary information and facilities to deliver quality products to Client Sites.Certifies product builders to ensure they have the required skills to complete their operation.*This is not an exhaustive list of duties or functions and may not necessarily comprise all of the "essential functions" for purposes of the ADAEssential Requirements:Third Level Degree in Quality or Engineering field1 year service in ZOML (at start date)2 years relevant experience in a relevant quality technician role.Excellent communication and influencing skills.Microsoft Office Suite.Understanding of QSR/ISO regulationsRisk assessment skills using FMEA methodologyProduct testing methods, and able to use hard gaging and optical comparators.Knowledge of statistics, process control, and process capability.Demonstrated NCR / CAPA experienceAbility to work within a team environment and build relationships outside of the department as well as outside the company (suppliers, regulatory agencies, etc.).Facilitates team efforts on quality engineering projects.Ability to deliver, meet deadlines and have results orientation.Able to communicate both orally and in written form to multiple levels of the comp Desirables:Demonstrated history of taking initiative, meeting commitments and assisting in the creation of new tools or solutions to achieve business results.New Product Introduction / Product transfer experienceProcess / software validation Experience For further information on this role please contact Shane Connolly on (phone number removed) or Check out all our open jobs on our HERO Recruitment website
Data Quality Engineer
, Galway, County Galway, Republic of
Data Quality Engineer
IT Support Engineer
MERIT EPOS SYSTEMS LIMITED, Claregalway, Lakeview, County Galway
Application Details Share This work experience programme provides Participants with an opportunity to gain meaningful work experience, learning and training while on the programme. This programme is for jobseekers that are in receipt of qualifying social welfare payments and those transferring from a social welfare scheme. Your eligibility for this programme will have to be verified by the Department as part of the application process. If you are in receipt of the Pandemic Unemployment Payment (PUP) you will be required to transfer to a Jobseekers payment in order to participate on the programme. Job Description Due to continued growth and expansion JBMMerit Epos Systems has an exciting opportunity for an IT Support Technician to join our team at our Galway officesThe candidate will play a role in supporting, maintaining and monitoring our customer base in the day-to-day operations of their Point of Sale systems.The placement is ideally suited to:•Highly motivated individual with the ability to communicate effectively to their mentor and their team.•A candidate possessing a strong work ethic attitude •Candidates must be hard working, flexible and adaptable to meet the demands of the day to day running of the business•Passionate, enthusiastic and committed to maintaining our excellent customer service•Excellent written & verbal communication skills•Comfortable with the use of computers for a variety of tasks•Competent in Microsoft applications, including word, excel and outlook•Good analytical & problem solving skills•A candidate with a willingness to learnMentor assisted tasks will including the follow•Provide first line support to customers on hardware and software with a primary focus on phone, email, remote on-line and call-out•Assisting the mentor with troubleshooting POS software and hardware, Networking and Desktop hardware/software support•Logging calls & keeping records of customer queries•Carry out installations, training and maintenance on POS systems and associated equipment•Maintain client records•Liaising with mentor regarding diary dates for provision of customer support•Escalate issues to other departments when needed•Comfortable liaising with technical & non-technical personnel•Observing and shadowing mentor as they liaise with third party vendors for software / hardware installations•Working closely with mentor to ensure communications with customers are prompt until queries are brought to a satisfactory outcome•Giving our clients an overall quality customer service experience•Reviewing customer calls with your mentor to identify common issues• Must speak fluent English Role Description The participant will receive formal/ informal training and mentoring as follows: The day to day Point of Sale operations of a busy retail forecourt and convenience store business. The logic of Point of Sale features and functionality which are necessary for succesful business operations of our customers. The tools necessary to use to provide first line support over the phone and via remote dial in. Initial troubleshooting for routine scenarios that are likely to occur, the protocols to follow to escalate a call for further attention. The participant will receive training on the supporting infrastructure of the Point of Sale software including the relational database and supporting software. Career Level Not Required Candidate Requirements Essential Minimum Experienced Required (Years): 0
Software Quality Assurance Engineer
We are looking for a Software Quality Assurance Engineer to develop and execute end to end functional tests (manual and automated) in order to ensure product quality for our core cloud offer. The Software Quality Assurance Engineer responsibilities include estimating, planning, and coordinating testing activities as well as test execution and reporting. You will also ensure that quality issues and defects are appropriately identified, documented, tracked, and resolved in our defect tracking system. GCS Computer Recruitment Services is acting as an Employment Business in relation to this vacancy.
Senior Quality Engineer
Title: Senior Quality EngineerLocation: Ballybrit, GalwayBenefits: Competitive salary, Healthcare, Pension, yearly bonus, an opportunity to grow your career with one of the biggest Medical Device companies in the world.Responsibilities:Select appropriate techniques for problem solving and make solid and consistent Engineering and Quality Assurance recommendations.Have the responsibility and authority to make decisions related to product quality including the disposition of non-conforming product.Participate in Customer Complaints investigation for areas under your control.Demonstrate and actively promote highest level of professional QA Engineering discipline and rigor.Be a leader in QSR, ISO / MDD standards within your group, be constantly aware of best industry practices. Have significant expertise in validation engineering and be familiar with all regulatory requirements.Review and approve operational, test and validation data to establish technical specifications and performance standards for newly designed or modified products and processes.Champion continuous improvement and innovation from a quality perspective within the department from vendor selection through to customer awareness/satisfaction.Be an effective team member, be fully motivated to achieve and demonstrate best practices in line with the department and LRP Objectives.Deals with suppliers, other engineering disciplines within and outside of Site and customers should the need arise.Provide technical guidance to Quality Engineer, Associate Quality Engineers, technicians and inspection staff.Requirements:A Level 8 Degree (240 Credits) or equivalent in an Engineering or Science related discipline.A minimum of 8 years' relevant experience, ideally within the Medical Device industry or another highly regulated environment.What my client can offer:A Career with Meaningful Purpose - opportunity to transform the lives of patients worldwideOur Culture - our work is guided by core values that define our culture and empower our employees.Career Development - our highly engaged leaders will empower you to grow and will invest in your potential. You can also broaden your skills through personal development courses.Opportunity to Innovate - we encourage you to fulfil your true creative potential by speaking up with your ideas and solutions to problems that matter.Competitive Benefits - we offer market leading benefits including performance-related bonus, pension contribution and healthcare.Work-Life Balance - we have created a culture that acknowledges, respects and supports your life and work choices.Corporate Social Responsibility - we are dedicated to progressing business practices in areas important to our communities. Our onsite charity events have raised over €1.5 million for worthy causes in the past ten years. If you are interested in applying/ finding out more about this opportunity and others like it forward me an up to date CV of contact me on the details provided to arrange a call. I am happy to answer any questions.Look forward to hearing from you.To find out more about Real please visit Real Staffing, a trading division of SThree Partnership LLP is acting as an Employment Agency in relation to this vacancy| Registered office | 1st Floor, 75 King William Street, London, EC4N 7BE, United Kingdom | Partnership Number | OC(phone number removed) England and Wales
Senior Full Stack Engineer
Snr Software Engineer to join a talented team developing game-changing business management solution includes fleet management and analysis web application (a SaaS offering, deployed on Amazon) and apps on Android mobile devicesIf you are a quick learner who really enjoys problem-solving and writing high-quality code using leading-edge technologies and modern development practices, then this is a great match.You will:· Produce state of the art technical designs, software, test, and document assets· Evaluate technologies, innovate on product architecture· Be a strong advocate of good agile development practices - code reviews,automated test, continuous integration, continuous delivery· Work closely with developers, QA team, customer support and product management on delivering and supporting our service.What we need to see:· A Bachelor or higher degree in Computer Science or related field· 5+ years of experienced full-stack development in web and/or mobile applications· Commercial experience in Database Schema Design· Good knowledge of frameworks such as Spring, Angular JS· Great object-oriented skills and knowledge of design patterns· Experience in an agile development environment with TDD, continuous integration and continuous delivery, using tools such as Cucumber, Git, Jenkins and Docker· Good verbal and written communication skills· Excellent problem-solving skills and attention to detailWays to stand out from the crowd:· Experience/strong interest in some of the following:· Security· Android development· Microservice architectures· Message queue/broker / MQTT· Amazon Web Services / Serverless architecture· IoT· Developing automated test frameworks· Database Query Optimisation· UX experienceIf you are a quick learner who really enjoys problem-solving and writing high-quality code using leading-edge technologies and modern development practices, then this is a great match.You will:· Produce state of the art technical designs, software, test, and document assets· Evaluate technologies, innovate on product architecture· Be a strong advocate of good agile development practices - code reviews, automated test, continuous integration, continuous delivery· Work closely with developers, QA team, customer support, and product management on delivering and supporting our service.What we need to see:· A Bachelor or higher degree in Computer Science or related field· 5+ years of experience full-stack development in web and/or mobile applications· Commercial experience in Database Schema Design· Good knowledge of frameworks such as Spring, Angular JS· Great object-oriented skills and knowledge of design patterns· Experience in an agile development environment with TDD, continuous integration and continuous delivery, using tools such as Cucumber, Git, Jenkins and Docker· Good verbal and written communication skills· Excellent problem-solving skills and attention to detailWays to stand out from the crowd:· Experience/strong interest in some of the following:· Security· Android development· Microservice architectures· Message queue/broker / MQTT· Amazon Web Services / Serverless architecture· IoT· Developing automated test frameworks· Database Query Optimisation· UX experience