156 Manufacturing Engineer Quality Engineer jobs in Ireland

Are you ready to make a real impact? We're seeking a Design Quality Engineer to ensure that next-generation medical technologies meet the highest standards of safety, compliance, and innovation. About the Role As a Design Quality Engineer, you'll be at the heart of new product development-driving quality, leading risk management activities, and ensuring compliance with global regulatory standards. You'll collaborate with R&D, Design, manufacturing and regulatory teams to bring safe, effective, and life-changing products from concept to launch. What You'll Do Lead risk management activities (UFMEA, DFMEA, PFMEA) and maintain documentation Ensure design control compliance across all NPD projects Perform statistical analysis (DOE, process optimisation, variation resolution) and initiate corrective actions Support biocompatibility testing per ISO 10993 Contribute to internal and supplier audits Validate test methods and measurement systems (Gauge R&R, TMV) Champion a culture of quality and compliance throughout the product lifecycle What We're Looking For Degree in Engineering, Science, or a technical field 5+ years' experience in the medical device or pharmaceutical industry Strong knowledge of ISO 13485, ISO 14971, ISO 10993, and relevant CFRs Detail-oriented, adaptable, and a natural problem solver Ability to manage multiple projects while thriving in a collaborative team environment Why Apply? Be part of creating products that improve and save lives Work in a culture of innovation, growth, and purpose Enjoy career development opportunities in a fast-moving, global industry with a healthy pipeline of projects Take the next step in your career and help shape the future of healthcare. Apply today! Design Quality Engineer, Quality Engineer, Design Quality Engineer, Quality Assurance Engineer Skills: Design engineer quality engineer GMP Benefits: Pension Healthcare enhanced AL

We are seeking an experienced Product Quality Engineerto join our clients growing team.

This is a pivotal role working across R&D, Quality, Production, and Test Engineering, ensuring that both hardware and software product designs meet the highest standards of quality, reliability, and compliance.

The ideal candidate will have strong technical expertise, hands-on experience with product development, and the ability to influence design processes from concept through to launch and beyond.

Responsibilities Collaborate with R&D teams to assess and influence product designs for quality, reliability, and compliance.

Review schematics, PCB layouts, and hardware specifications to identify potential design risks.

Lead design risk assessments (DFMEA) and support root cause analysis activities.

Support validation and verification for new product introductions.

Partner with Purchasing and R&D teams to qualify new vendors and parts.

Perform statistical analysis and reporting of test data.

Support hardware and software testing from a quality perspective.

Provide technical support to Production, Test, and Process Quality teams to resolve product-related issues.

Act as a technical quality representative in design reviews and development meetings.

Support audits and inspections related to design controls.

Drive continuous improvement in design processes and quality metrics.

Requirements: Bachelors degree in Electronic, Electrical, Software Engineering, or related field.

5+ years experiencein a Quality or R&D role within a regulated industry (medical devices, aerospace, automotive, or life safety).

Strong understanding of product development lifecycle and design controls.

Experience with hardware/software integration and testing.

Familiarity with ISO 9001 or similar quality management systems.

Ability to interpret electronic schematics, circuit designs, and technical specifications.

Skilled in FMEA, risk management, and root cause analysis.

Knowledge of embedded systems, firmware, or software development.

Strong communication and cross-functional collaboration skills.

For a confidential conversation about the role contact Owen Clancy at By applying to this job post you agree that Sterling Engineering may process your personal data for recruitment purpose

Supplier Quality Professional - Permanent Role Do you want to join us in helping to fight the world's most threatening diseases and enabling access to care for more people around the world? At Siemens Healthineers, we pioneer breakthroughs in healthcare.

For everyone.

Everywhere.

Sustainably.

We offer you a flexible and dynamic environment with opportunities to go beyond your comfort zone in order to grow personally and professionally.

Sound interesting? Then come and join our global team as Supplier Quality Professional at our facility in Swords, Co.

Dublin Your tasks and responsibilities: To develop world-class supply chain processes to suit a low volume, high complexity multi-technology environment (diagnostic instrumentation).

To manage our suppliers to deliver quality product to our internal customers, through product & process investigations & evaluations.

Liaising with a wide variety of external suppliers to ensure suppliers are trained and adhere to Siemens First Articles, Quality and Regulatory requirements.

Issuing of Supplier Corrective Action Reports and working with suppliers on Root Cause Investigations and Corrective action.

Conducting Supplier Performance Reviews and Reporting of Key Supplier Quality metrics.

To support technology transfer initiatives and new projects.

Involving the assessment and selection of new suppliers where applicable.

To provide day to day inspection expertise support to the Purchased Material Inspection Department (PMI) in the areas of Component and Mechatronic Inspection and acting as a technical reference to interface with the supplier.

To contribute to the continuous development of the quality system, including standard operating procedures (SOP's) coupled with the ability to write concise technical reports.

Support a Strong Supplier focus to ensure that that our requirements are met appropriately and oversee relevant KPIs for supplier quality oversight.

Internally supporting the demands of the instrument and spares supply manufacturing operation.

Working with external functional quality and supplier management groups within Siemens.

Utilizing and developing digitalization tools to identify areas for improvement and to streamline Quality reports.

To find out more about the specific business, have a look at Siemens Healthcare Diagnostics Manufacturing Limited - Swords (siemens- Your qualifications and experience: Ideally with 3 years + relevant experience.

Minimum of a third level qualification (Diploma/Degree) in an appropriate discipline (Quality Management, Mechatronics, Electronics or Mechanical Engineering) OR appropriate and commensurate experience.

Experience in leading and being a part of teams and projects with strong communications written and verbal.

Ability to work in technically complex multi discipline areas across the whole supply chain, including the supplier environment Your attributes and skills: Mechanical, Mechatronic and Electromechanical measurement systems - Advanced Inspection Methodologies such as; Fabricated/Machined Metal Mechanical/Visual inspection, Precision linear measurement, non-contact measurement, Moulded and Machined plastics inspection and measurement - Advanced Geometrical Tolerancing (e.g.

true position, perpendicularity, concentricity, angularity, roundness etc.) - Advanced Interface with suppliers across technologies - Advanced Excellent Communication skills both oral and written - Expert Lead auditing experience to both ISO 9004:2015 and ISO - Advanced Ideally have a working knowledge of Six Sigma, Statistical Analysis and Lean principles for investigations, problem solving and continuous improvement Our global team: We are a team of more than 70,000 highly dedicated employees across more than 70 countries passionately pushing the boundaries of what's possible in healthcare to help improve people's lives around the world.

As a leader in the industry, we aspire to create better outcomes and experiences for patients no matter where they live or what health issues they are facing.

Our portfolio, spanning from in-vitro and in-vivo diagnostics to image-guided therapy and innovative cancer care, is crucial for clinical decision-making and treatment pathways.

Our culture: We are part of an incredible community of scientists, clinicians, developers, researchers, professionals, and skilled specialists pushing the boundaries of what's possible, to improve people's lives around the world.

We embrace a culture of inclusivity in which the power and potential of every individual can be unleashed.

We spark ideas that lead to positive impact and continued success.

Check our Careers Site at Jobs at Siemens Healthineers (siemens- #Siemens Please note: For candidates applying through Irishjobs, please ensure that you complete your application fully all the way through to Avature.

Failure to fully complete your application may result in Siemens not being able to view your CV.

Please find Avature link to this role below.

As an equal opportunity employer, we welcome applications from individuals with disabilities.

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Quality Engineer - Contract I'm looking for a proactive individual to work with my reputable client on an upcoming project on a daily rate contract basis.

This role will initially be for 6 months but will like offer further extension.

Its an excellent opportunity for an experienced quality engineer who is looking for their next role and can support an existing team in providing exceptional quality processes.

Requirements: Minimum of 5 years quality engineering experience Fantastic communication skills and ability to work effectively in an agile environment Strong manual testing experience (over 5 years) and API testing Finance/ payments experience would be advantageous Proven ability of working with CI/CD pipelines and working closely with developers I specialize in recruiting for QA and Software Testing, if you wish to discuss this or other Software Testing opportunities, please feel free to contact Rachel for a confidential chat.

Reperio Human Capital acts as an Employment Agency and an Employment Business.

Skills: qa engineer manual tester software tester functional tester Benefits: Work From Home

QA Automation Engineer - Financial Services, 6 Month Contract Location: Ireland, Hybrid (2 days onsite per week) Contract Length: Initial 6 Months Rate: €400 per day Industry: Financial Services I'm currently hiring for a 6-month daily rate QA contract with a leading Financial Services client.

This is a hybrid role, requiring 2 days onsite per week.

I'm looking for a proactive and motivated QA professional with 5+ years of experience to join a fast-paced Agile squad, supporting the testing of high-quality front-end web apps and APIs - with a strong emphasis on test automation.

What you'll be doing: Designing and executing both automated and manual test cases.

Collaborating closely with developers, BAs, and fellow QAs in a supportive Agile environment.

Presenting progress updates in daily stand-ups and small group sessions.

Maintaining and improving a scalable automation framework.

What my client is looking for: Solid QA background (3+ years), ideally in Agile environments.

Experience with tools like Cypress, Tosca, or Postman is highly desirable (but not essential).

Strong communication skills and a collaborative mindset.

Ability to hit the ground running with minimal handholding.

Experience in Financial Services is a bonus.

Additional Information Immediate interviews with prompt start date available.

Applicants must be eligible to work full-time in Ireland without restrictions.

For more information, please contact Scott Hool in confidence.

Reperio Human Capital acts as an Employment Agency and an Employment Business.

Skills: Test Automation Engineer Cypress Contract

Embecta is a global diabetes care company that is leveraging its 100-year legacy in insulin delivery to empower people with diabetes to live their best life through innovative solutions, partnerships and the passion of more than 2,000 employees around the globe.

Why join us? A career at embecta means being part of a team that values your opinions and contributions and that empowers you to bring your authentic self to work.

Here our employees can fulfill their life's purpose through the work that they do every day.

You will learn and work alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture.

Our Total Rewards program - which includes competitive pay, benefits, continuous learning, recognition, career growth and life balance components - is designed to support the varying needs of our diverse and global employees.

In this role the Shift Quality Engineer ensures quality engineering support for daily manufacturing operations, collaborating with the Quality Engineering team and Shift QC Leads to meet business quality standards.

The position follows a 7am-7pm schedule on a 4-day rotating basis, with occasional night shift coverage as needed.

Managing the activities of the Quality Inspectors to ensure optimal efficiency and compliance with all regulatory requirements.

Drive root cause analysis of non-conformances with relevant personnel and ensure corrections are implemented before starting back to production after a quality issue.

Drive and maintain c GMP practices across all operational departments under your quality responsibility (Incoming, moulding, assembly, packaging sterilization, warehouse) and attend departmental and other meetings as appropriate.

Preparation of relevant work sheets and execution of final inspection tests and line clearance verification.

Release batches in SAP from packaging to sterilization and final release.

Complete DHR reviews and batch releases.

Provide GMP guidance in case of rework and/or inspection protocols.

Line clearance verification.

Complete Product Quality Testing Ensure that maintenance records and process adjustments records are maintained and captured in real time.

Ensure all CAPAs under your responsibility are completed in compliance with all regulatory and procedural commitments.

Participate in the Change Control Process.

Liaise with relevant personnel regarding flow of product through QC department and other issues that arise Preparation, review and approval of technical documentation.

Manage and provide support with ongoing changes and continuous improvement projects Perform training as required Ensure the smooth running of functions under your control Review, analyze and report on relevant customer complaints and institute corrective actions Any other reasonable duties which may be required by management from time to time Educational Requirements: Third level qualification in a Science/Engineering discipline Relevant Experience: Strong knowledge and application ISO 9001/2000 or ISO 13485 environment.

Demonstrable experience in the preparation of Technical Documentation.

Understanding of Statistical Process Control and sampling techniques and standards Experience with SAP and Trackwise is beneficial Good experience in CAPA system management, incident report and MRB Working knowledge of general validation activities Experience in complaints analysis and reporting A working knowledge of FDA requirements and managing FDA audits.

Proven ability of working in a cross-functional team environment.

Excellent interpersonal and communication skills.

High level of computer literacy.

embecta is an Equal Opportunity/Affirmative Action Employer.

We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.

Are you ready to make a real impact? We're seeking a Design Quality Engineer to ensure that next-generation medical technologies meet the highest standards of safety, compliance, and innovation.

About the Role As a Design Quality Engineer, you'll be at the heart of new product development-driving quality, leading risk management activities, and ensuring compliance with global regulatory standards.

You'll collaborate with R&D, Design, manufacturing and regulatory teams to bring safe, effective, and life-changing products from concept to launch.

What You'll Do Lead risk management activities (UFMEA, DFMEA, PFMEA) and maintain documentation Ensure design control compliance across all NPD projects Perform statistical analysis (DOE, process optimisation, variation resolution) and initiate corrective actions Support biocompatibility testing per ISO 10993 Contribute to internal and supplier audits Validate test methods and measurement systems (Gauge R&R, TMV) Champion a culture of quality and compliance throughout the product lifecycle What We're Looking For Degree in Engineering, Science, or a technical field 5+ years' experience in the medical device or pharmaceutical industry Strong knowledge of ISO 13485, ISO 14971, ISO 10993, and relevant CFRs Detail-oriented, adaptable, and a natural problem solver Ability to manage multiple projects while thriving in a collaborative team environment Why Apply? Be part of creating products that improve and save lives Work in a culture of innovation, growth, and purpose Enjoy career development opportunities in a fast-moving, global industry with a healthy pipeline of projects Take the next step in your career and help shape the future of healthcare.

Apply today! Design Quality Engineer, Quality Engineer, Design Quality Engineer, Quality Assurance Engineer Skills: Design engineer quality engineer GMP Benefits: Pension Healthcare enhanced AL

At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient's mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds.
As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talent team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels included, respected, empowered and recognised.
**What You Can Expect**
Responsible for assuring products conform to established requirements and standards through appropriate audit, inspection, and test activities. This includes analysing quality trend data and taking appropriate action; supporting production on all quality related issues; investigating customer complaints; qualifying, auditing and monitoring suppliers and ensuring an effective and robust quality system which complies with all relevant regulatory requirements; Interacts with many different functional departments, suppliers, and experts outside Zimmer to implement Zimmer Quality goals.
**How You'll Create Impact**
+ Formulates procedures, specifications, and standards for Zimmer 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 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 Zimmer.
+ Evaluates new suppliers as required and co-ordinate supplier corrective actions where necessary.
+ Ensures that the Receiving inspection process is implemented in a complaint and effective manner.
**What Makes You Stand Out**
+ Microsoft Office Suite.
+ Expert knowledge of blueprint reading and geometric dimensioning and tolerancing.
+ Understanding of QSR/ISO regulations
+ Quality system auditing techniques.
+ Design assurance, FMEA, and product testing methods, and able to use optical comparators and CMMs.
+ Knowledge of statistics, process control, and process capability.
+ Ability 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 company.
**Your Background**
+ Third level degree in engineering or Science degree.
+ Certification as a quality engineer (e.g. CQE) is preferred.
**12 Month Fixed Term**
EOE/M/F/Vet/Disability

It all started in sunny San Diego, California in 2004 when a visionary engineer, Fred Luddy, saw the potential to transform how we work. Fast forward to today - ServiceNow stands as a global market leader, bringing innovative AI-enhanced technology to over 8,100 customers, including 85% of the Fortune 500®. Our intelligent cloud-based platform seamlessly connects people, systems, and processes to empower organizations to find smarter, faster, and better ways to work. But this is just the beginning of our journey. Join us as we pursue our purpose to make the world work better for everyone.
**What you get to do in this role:** **  **
+ Maintain existing automation test frameworks
+ Collect and report quality metrics from test execution
+ Work with developers to design specific testing strategies for features being developed and automate them
+ Create comprehensive test plans; execute and automate them
+ Support engineering organizations in troubleshooting or addressing issues with applications and dev/test environments
**To be successful in this role you have:**
+ Experience in leveraging or critically thinking about how to integrate AI into work processes, decision-making, or problem-solving. This may include using AI-powered tools, automating workflows, analyzing AI-driven insights, or exploring AI's potential impact on the function or industry.
+ 5+ years of experience with quality assurance and Java programming with Selenium, JUnit and TestNG
+ Fluency with scripting in JavaScript. Experience with Eclipse, Jenkin, Maven, and Git
+ Understanding of testing techniques (e.g. performance, unit, integration, automated), their strengths and weakness, and ability to use them to best effect
+ Ability to use tools (such as IDE, debugger, build tools, source control, ServiceNow instances, profilers, system administration/Unix tools) to assist with daily tasks
+ Experience driving cross-team technical discussions with an understanding of SDLC concepts
**Work Personas**
We approach our distributed world of work with flexibility and trust. Work personas (flexible, remote, or required in office) are categories that are assigned to ServiceNow employees depending on the nature of their work and their assigned work location. Learn more here ( . To determine eligibility for a work persona, ServiceNow may confirm the distance between your primary residence and the closest ServiceNow office using a third-party service.
**Equal Opportunity Employer**
ServiceNow is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, creed, religion, sex, sexual orientation, national origin or nationality, ancestry, age, disability, gender identity or expression, marital status, veteran status, or any other category protected by law. In addition, all qualified applicants with arrest or conviction records will be considered for employment in accordance with legal requirements.
**Accommodations**
We strive to create an accessible and inclusive experience for all candidates. If you require a reasonable accommodation to complete any part of the application process, or are unable to use this online application and need an alternative method to apply, please contact for assistance.
**Export Control Regulations**
For positions requiring access to controlled technology subject to export control regulations, including the U.S. Export Administration Regulations (EAR), ServiceNow may be required to obtain export control approval from government authorities for certain individuals. All employment is contingent upon ServiceNow obtaining any export license or other approval that may be required by relevant export control authorities.
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