What Principal R D Engineer Crdn Jobs are in ...Showing 8 Principal R D Engineer Crdn jobs in GalwayAt Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You'll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.**A Day in the Life**We are looking for a Principal R&D engineer with a proven track record of experience and success with respect to polymers and extrusions for medical manufacturing to join our Coronary & Renal Denervation (CRDN) therapies are a vital component of the Medtronic interventional cardiology portfolio. In addition to our core products that treat blocked coronary arteries, we are seeking to solve unmet needs in the rapidly growing field of complex Percutaneous Coronary Intervention (PCI). We are also leading the way with the transformational Blood pressure reduction therapy, which has the potential to be a powerful tool in battling the global hypertension epidemic.If you want a challenging, energizing, rewarding career that changes lives, join us. Help us bring the next generation of life-changing medical technology to patients worldwide.Extensive engineering knowledge and skills in some or all of the following: component and system design, materials (polymers and metals), sterilization of medical devices, test method development, design for six sigma principles, CAD (Solidworks preferred), pre-clinical evaluations, physician interactions, knowledge of anatomical use conditions (anatomy, physiology etc.), system requirements development, design control, application of ISO standards for medical devices**A Day in The Life Of:**+ Design, develop, troubleshoot, and provides technical skills during research and / or product development+ Effectively represent Medtronic while interacting with physicians to distil their needs into product requirements and concepts+ Provide direction in technical innovation across the department+ Identify and mitigate technological risks throughout the design process+ Apply understanding of anatomy & physiology with engineering knowledge in materials and processes to come up with working designs+ Interface effectively and build relationships with team members, other staff and key technology and component suppliers, both locally and globally+ May be required to progress a project from concept phase into commercialization phase and play a key role on the product / process / engineering / technical fronts+ May be required to resolve technical obstacles with existing designs and support portfolio sustaining activities+ Continually contribute to generation of intellectual property+ Coach, mentor, and delegate work to less experienced engineers+ Partake in cross site Technical Forums and build a network within the technical community+ Define and implement strategic goals in the technical community in line with the business unit strategy+ Design studies to investigate specific life science questions within field of expertise**Key Skills & Experience**+ Degree level 8 in Engineering or related discipline with a minimum 7 years of relevant experience, or PHD with a minimum of 5 years of relevant experience - additional relevant qualifications may be advantageous+ We are looking for a dynamic team player that can work effectively and proactively on cross-functional teams+ We are looking for an engineer with extensive medical device product development experience and a strong proven track record in innovation and technical advisory+ This role is primarily technical in nature; thus, we seek someone who is passionate about Engineering concepts and principles - someone who gets a thrill from how and why things work+ We are looking for a proven influencer and someone who exhibit skills in driving large scale technical initiatives+ We are looking for strong communication and presentation skills+ A seasoned professional in engineering development with extensive engineering knowledge and skills in some or all of the following: component and system design, materials (polymers and metals), sterilization of medical devices, test method development, design for six sigma principles, CAD (Solidworks preferred), pre-clinical evaluations, physician interactions, knowledge of anatomical use conditions (anatomy, physiology etc.), system requirements development, design control, application of ISO standards for medical devices**Physical Job Requirements**The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.**Benefits & Compensation****Medtronic offers a competitive Salary and flexible Benefits Package**A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.Pay range / Rango salarial / Intervalo salarial /Fascia retributiva / Tranche de salaire / Gehaltsband / Salaribereik: Ireland: 81,120.00 EUR - 121,680.00 EUR |This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).**About Medtronic**We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.Our Mission - to alleviate pain, restore health, and extend life - unites a global team of 95,000+ passionate people.We are engineers at heart- putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.Learn more about our business, mission, and our commitment to diversity here ( lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.Our Mission - to alleviate pain, restore health, and extend life - unites a global team of 95,000+ passionate people.We are engineers at heart- putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.**We change lives**. Each team member, each day, helps to improve and redefine how the world treats the most pressing health conditions, from heart disease to diabetes. Our industry leadership comes from the passion and ingenuity of our people. That's who we are. Working alongside one another, we use science, medicine, and a profound understanding of the human body to build extraordinary technologies that can transform lives.**We build extraordinary solutions as one team**. With one Medtronic Mindset defining how we work. Speed and decisiveness run through our DNA. Diverse perspectives inspire our bold answers to any challenge that comes our way. And we deliver results the right way, breakthrough after patient breakthrough.**This life-changing career is yours to engineer**. By bringing your ambitious ideas, unique perspective and contributions, you will.+ **Build** a better future, amplifying your impact on the causes that matter to you and the world+ **Grow** a career reflective of your passion and abilities+ **Connect** to a dynamic and inclusive culture that welcomes the challenge of life-long learningThese commitments set our team apart from the rest:**Experiences that put people first**. Respect for people is the hallmark of our humanity. It fuels our team to positively impact even a single life. And it means we put our people first at Medtronic as well, creating a culture of belonging and always pushing to get you the career-building resources you need.**Life-transforming technologies**. No matter your role, you contribute to technologies that transform lives. What we build empowers patients to live life on their terms.**Better outcomes for our world**. Here, it's about more than the bottom line. Our Mission to improve human welfare drives us. We advance healthcare, society, and equity with every design, inside and outside our walls.**Insight-driven care**. Fresh viewpoints. Cutting-edge AI, data, and automation. You're shaping the future of healthcare technology and defining the next generation of breakthroughs in careIt is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.For sales reps and other patient facing field employees, going into a healthcare settingis considered an essential function of the job and we expect our employees to comply with all credentialing requirements at the hospitals or clinics they support.This employer participates in the federal E-Verify program to confirm the identity and employment authorization of all newly hired employees. For further information about the E-Verify program, please click here ( .For updates on job applications, please go to the candidate login page and sign in to check your application status.If you need assistance completing your application please emailTo request removal of your personal information from our systems please emailIs this job a match or a miss?Principal Biomedical Electronics Engineer - CRDNAt Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You'll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.**A Day in the Life**We are looking for a Principal Biomedical Engineer with a background in electronics who will serve as a technical leader in the design, development, and optimization of next-generation RF (Radiofrequency) ablation systems. This role focuses on high-frequency generator design, catheter integration, and the sophisticated control algorithms required applications in the renal denervation business. You will work with our research team to identify opportunities to improve device design to meet new and expanding customer needs.This Principal R&D engineer will have experience in development with extensive engineering knowledge and skills in some or all of the following: Design of electronic Class II and Class III devices for medical applications, therapy application of ablation RF systems, algorithm development, test method development, pre-clinical evaluations knowledge of anatomical use conditions (anatomy, physiology etc.), system requirements development, design control, application of ISO standards for medical devices.If you want a challenging, energizing, rewarding career that changes lives, join us. Help us bring the next generation of life-changing medical technology to patients worldwide. This role has a 4 day onsite requirement.**_Come for a job, stay for a career!_****A Day in The Life Of:**+ Design, develop, troubleshoot, and provides technical skills during research and / or product development+ Effectively represent Medtronic while interacting with physicians to distil their needs into product requirements and concepts+ Provide direction in technical innovation across the development teams+ Identify and mitigate technological risks throughout the design process+ Apply understanding of anatomy & physiology with engineering knowledge to come up with new design solutions to improve device performance and function+ Interface effectively and build relationships with team members, other staff and key technology and component suppliers, both locally and globally+ Progress a project from concept phase into commercialization phase and play a key role on the product / process / engineering / technical fronts+ Resolve technical obstacles with existing designs and support portfolio sustaining activities+ Continually contribute to generation of intellectual property+ Coach, mentor, and delegate work to less experienced engineers+ Partake in cross site Technical Forums and build a network within the technical community+ Define and implement strategic goals in the technical community in line with the business unit strategy**Key Skills & Experience**+ Degree level 8 in Engineering or related discipline with a minimum 7 years of relevant experience, or PHD with a minimum of 5 years of relevant experience - additional relevant qualifications may be advantageous.+ A dynamic team player that can work effectively and proactively on cross-functional teams+ A proven track record in innovation and technical advisory with complex problem solving+ Ability understand and develop complex systems that involve electronics, mechanics and algorithms to function+ We are looking for strong communication and presentation skills+ Continually contribute to generation of intellectual property+ Coach, mentor, and delegate work to less experienced engineers+ Partake in cross site Technical Forums and build a network within the technical community+ Define and implement strategic goals in the technical community in line with the business unit strategy**Medtronic offer a competitive salary and flexible Benefits Package****Physical Job Requirements**The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.**Benefits & Compensation****Medtronic offers a competitive Salary and flexible Benefits Package**A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.Pay range / Rango salarial / Intervalo salarial /Fascia retributiva / Tranche de salaire / Gehaltsband / Salaribereik: Ireland: 81,120.00 EUR - 121,680.00 EUR |This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).**About Medtronic**We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.Our Mission - to alleviate pain, restore health, and extend life - unites a global team of 95,000+ passionate people.We are engineers at heart- putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.Learn more about our business, mission, and our commitment to diversity here ( lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.Our Mission - to alleviate pain, restore health, and extend life - unites a global team of 95,000+ passionate people.We are engineers at heart- putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.**We change lives**. Each team member, each day, helps to improve and redefine how the world treats the most pressing health conditions, from heart disease to diabetes. Our industry leadership comes from the passion and ingenuity of our people. That's who we are. Working alongside one another, we use science, medicine, and a profound understanding of the human body to build extraordinary technologies that can transform lives.**We build extraordinary solutions as one team**. With one Medtronic Mindset defining how we work. Speed and decisiveness run through our DNA. Diverse perspectives inspire our bold answers to any challenge that comes our way. And we deliver results the right way, breakthrough after patient breakthrough.**This life-changing career is yours to engineer**. By bringing your ambitious ideas, unique perspective and contributions, you will.+ **Build** a better future, amplifying your impact on the causes that matter to you and the world+ **Grow** a career reflective of your passion and abilities+ **Connect** to a dynamic and inclusive culture that welcomes the challenge of life-long learningThese commitments set our team apart from the rest:**Experiences that put people first**. Respect for people is the hallmark of our humanity. It fuels our team to positively impact even a single life. And it means we put our people first at Medtronic as well, creating a culture of belonging and always pushing to get you the career-building resources you need.**Life-transforming technologies**. No matter your role, you contribute to technologies that transform lives. What we build empowers patients to live life on their terms.**Better outcomes for our world**. Here, it's about more than the bottom line. Our Mission to improve human welfare drives us. We advance healthcare, society, and equity with every design, inside and outside our walls.**Insight-driven care**. Fresh viewpoints. Cutting-edge AI, data, and automation. You're shaping the future of healthcare technology and defining the next generation of breakthroughs in careIt is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.For sales reps and other patient facing field employees, going into a healthcare settingis considered an essential function of the job and we expect our employees to comply with all credentialing requirements at the hospitals or clinics they support.This employer participates in the federal E-Verify program to confirm the identity and employment authorization of all newly hired employees. For further information about the E-Verify program, please click here ( .For updates on job applications, please go to the candidate login page and sign in to check your application status.If you need assistance completing your application please emailTo request removal of your personal information from our systems please emailIs this job a match or a miss?Principal Software Engineer - Framework - Patient Care SystemsIs this job a match or a miss?Principal Mixed-Signal Hardware EngineerAt Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You'll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.**A Day in the Life****Medtronic**At Medtronic, we value what makes you unique. Be part of a company that thinks differently to solve problems, make progress, and deliver meaningful innovations.**Our Purpose**The Physiological Sensing R&D team is dedicated to the end-to-end development, continuous advancement, and clinical validation of innovative monitoring technologies that measure, interpret, and leverage physiological signals to improve patient outcomes. Their expertise spans anesthesia and depth of sedation monitoring, respiratory monitoring, pulse oximetry, regional oximetry, and the integration of predictive algorithms and clinical decision support solutions. By focusing on non-invasive, real-time technologies, they empower clinicians with actionable insights in surgery, critical care, and other high-risk settings.**_Come for a job, stay for a career!_****A Day in The Life Of:**The Principal Electronics Hardware Engineer role carries strong leadership expectations, including influencing platform and design decisions, ensuring electronics solutions meet performance, safety, quality, and regulatory requirements throughout the product lifecycle, and mentoring engineers.+ Lead the architecture, design, and development of digital and analog electronics for physiologic monitoring devices and subsystems used in product development and research applications compliant with IEC 60601 for safety and essential performance of medical electrical equipment.+ Digital and analog electronics development activities for product development and research applications across physiologic monitoring systems and subsystems, such as pulse oximetry, regional oximetry, EEG based devices, and other sensing technologies.+ Define hardware technical direction, design standards, and architectural approaches aligned with system requirements and long‑term platform strategies.+ Provide hands-on technical leadership for schematic design, component selection, circuit simulation, and tolerance analysis.+ Guide PCBA development, including layout collaboration, signal and power integrity, EMC/ESD considerations, and stack-up definition.+ Lead electrical bring-up, debugging, characterization, and verification of prototypes and production-representative hardware.+ Collaborate cross-functionally with systems, software, algorithm, test, mechanical, and manufacturing engineers to ensure cohesive, testable designs.+ Support quality and regulatory activities through documentation, risk analysis, and verification evidence for medical device submissions.**Key Skills & Experience**+ Requires a Bachelors degree and minimum of 7 years of relevant experience OR Master's degree with a minimum of 5 years relevant experience OR PhD with 3 years relevant experience.+ Deep expertise in digital, analog, and mixed‑signal circuit design for complex, high‑reliability electronic systems.+ Expertise in low-signal analog circuit development, noise mitigation, and analog/digital signal processing desired.+ Proven experience defining hardware architecture and technical direction for complex products or platforms.+ Strong hands-on skills in schematic capture, component selection, circuit simulation, and tolerance analysis.+ Extensive experience guiding PCBA development, including layout collaboration, stack-up definition, and design for signal integrity, power integrity, and EMC/ESD.+ Experience leading hardware bring-up, debugging, characterization, and failure analysis of prototype and production-representative boards.+ Strong understanding of electrical verification and validation methods, test equipment, and correlation to system-level requirements.+ Experience working in regulated product development environments; familiarity with medical device hardware development and quality systems preferred.+ Ability to resolve complex, ambiguous, or cross-disciplinary technical challenges spanning electronics, systems, and manufacturing constraints.+ Strong technical review and mentoring skills, including design reviews and technical guidance without direct people management responsibilities.+ Effective communication skills, with the ability to clearly explain technical tradeoffs, risks, and recommendations to cross-functional stakeholders.**Medtronic offer a competitive salary and flexible Benefits Package****Physical Job Requirements**The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.**Benefits & Compensation****Medtronic offers a competitive Salary and flexible Benefits Package**A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.Pay range / Rango salarial / Intervalo salarial /Fascia retributiva / Tranche de salaire / Gehaltsband / Salaribereik: Ireland: 81,120.00 EUR - 121,680.00 EUR |This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).**About Medtronic**We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.Our Mission - to alleviate pain, restore health, and extend life - unites a global team of 95,000+ passionate people.We are engineers at heart- putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.Learn more about our business, mission, and our commitment to diversity here ( lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.Our Mission - to alleviate pain, restore health, and extend life - unites a global team of 95,000+ passionate people.We are engineers at heart- putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.**We change lives**. Each team member, each day, helps to improve and redefine how the world treats the most pressing health conditions, from heart disease to diabetes. Our industry leadership comes from the passion and ingenuity of our people. That's who we are. Working alongside one another, we use science, medicine, and a profound understanding of the human body to build extraordinary technologies that can transform lives.**We build extraordinary solutions as one team**. With one Medtronic Mindset defining how we work. Speed and decisiveness run through our DNA. Diverse perspectives inspire our bold answers to any challenge that comes our way. And we deliver results the right way, breakthrough after patient breakthrough.**This life-changing career is yours to engineer**. By bringing your ambitious ideas, unique perspective and contributions, you will.+ **Build** a better future, amplifying your impact on the causes that matter to you and the world+ **Grow** a career reflective of your passion and abilities+ **Connect** to a dynamic and inclusive culture that welcomes the challenge of life-long learningThese commitments set our team apart from the rest:**Experiences that put people first**. Respect for people is the hallmark of our humanity. It fuels our team to positively impact even a single life. And it means we put our people first at Medtronic as well, creating a culture of belonging and always pushing to get you the career-building resources you need.**Life-transforming technologies**. No matter your role, you contribute to technologies that transform lives. What we build empowers patients to live life on their terms.**Better outcomes for our world**. Here, it's about more than the bottom line. Our Mission to improve human welfare drives us. We advance healthcare, society, and equity with every design, inside and outside our walls.**Insight-driven care**. Fresh viewpoints. Cutting-edge AI, data, and automation. You're shaping the future of healthcare technology and defining the next generation of breakthroughs in careIt is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.For sales reps and other patient facing field employees, going into a healthcare settingis considered an essential function of the job and we expect our employees to comply with all credentialing requirements at the hospitals or clinics they support.This employer participates in the federal E-Verify program to confirm the identity and employment authorization of all newly hired employees. For further information about the E-Verify program, please click here ( .For updates on job applications, please go to the candidate login page and sign in to check your application status.If you need assistance completing your application please emailTo request removal of your personal information from our systems please emailIs this job a match or a miss?Principal Engineer- Development Infrastructure**Company Description****Work with Us. Change the World.**At AECOM, we're delivering a better world. Whether improving your commute, keeping the lights on, providing access to clean water, or transforming skylines, our work helps people and communities thrive. We are the world's trusted infrastructure consulting firm, partnering with clients to solve the world's most complex challenges and build legacies for future generations.There has never been a better time to be at AECOM. With accelerating infrastructure investment worldwide, our services are in great demand. We invite you to bring your bold ideas and big dreams and become part of a global team of over 50,000 planners, designers, engineers, scientists, digital innovators, program and construction managers and other professionals delivering projects that create a positive and tangible impact around the world.We're one global team driven by our common purpose to deliver a better world. Join us.**Job Description****Start here. Grow here.**Are you ready to challenge the boundaries of what's possible? AECOM continues to expand their successful and established Infrastructure Development team in Ireland and requires a Principal Engineer to join the Dublin, Galway or Cork office in Ireland.**What can we offer?**The team has an established track record of successfully delivering development infrastructure schemes both locally and across Ireland and the U.K. Our wide range of clients includes developers, retailers, landowners, housebuilders, blue-chip companies, and Universities. Our current portfolio of work comprises a diverse mix of local and national development and civil infrastructure projects at all stages, from Feasibility through to Detailed Design and Construction_Here's what you'll do:_+ **Deliver:** Our wide range of clients includes local authorities, government agencies, developers, retailers, landowners, housebuilders, blue-chip companies, and Universities. You will be a part of a team that delivers high quality civil engineering support and services to all project stages, from feasibility through to Detailed Design and Construction.+ **Oversee:** You will take ownership of the tasks that are required for each of the project stages. You will work with other design team members whilst providing guidance to entry-level engineers and coordinated with the relevant multi-disciplinary teams to deliver engineering designs and deliverables for our clients, within programme and on budget.+ **Provide Expertise:** Offer technical knowledge and expertise on all aspects of multi-disciplinary projects, particularly drainage design, from conceptual phases to implementation.+ **Ensure Quality:** You will strive for excellence in all projects, following the AECOM QA/QC procedures and you will work through the complexities of projects by providing early warning on risks associated with programme and budget, and by working with the client to overcome project challenges.+ **Collaborate:** You will work with both internal and external multi-disciplinary engineers and stakeholder to allow you to successfully deliver integrated designs and build effective relationships to ensure the success of projects.**Come grow with us.**Let's not forget about the perks at AECOM. You'll enjoy a range of core and personalised benefits designed to support your future and well-being, customised to fit your lifestyle. Take advantage of career development opportunities, **our flexible hybrid working model to ensure a work-life balance that suits your lifestyle**, technical practice networks, AECOM University, and volunteering days.**Qualifications****Ready to push the limits of what's possible?**_Here's what we're looking for:_+ A Bachelor's Degree in Civil Engineering.+ Either Chartered or working towards Chartered status with the Institution of Engineers of Ireland or Institution of Civil Engineers or relevant Institution+ Relevant work experience in the design and delivery of civil infrastructure from inception to handover including experience in the design of SUDs, water main distribution pipelines, storm and foul gravity collection networks, surface water catchment analysis, flood risk assessments, highway and pavement design, earthworks modelling and working knowledge of DMRB and DMURS+ Experienced in using relevant industry-standard software including Microdrainage or InfoDrainage, AutoCAD and Civil 3d.+ Experience of working in a multidisciplinary design team, and capable of effectively liaising with architects, planning consultants, and external consultants.+ Experienced in undertaking site inspections, test witnessing and reporting on same, and answering technical RFIs during construction.We celebrate diversity, including neurodiversity, and believe it enriches our team. We welcome applications from all backgrounds and abilities. If you are an applicant with a disability that requires reasonable accommodation to complete the application process, please contact us atAt AECOM, we value everyone's unique contributions and perspectives.If you meet some of the requirements above or have transferable skills you believe would benefit us, we would be delighted to hear from you!**Additional Information**Interested in the role or curious about life at AECOM? Follow us on LinkedIn, Facebook, Instagram, and YouTube to explore our AECOM voices, employee stories, latest projects, and much more!\#EVB**About AECOM**AECOM is the world's trusted infrastructure consulting firm, delivering professional services throughout the project lifecycle - from advisory, planning, design and engineering to program and construction management. On projects spanning transportation, buildings, water, new energy and the environment, our public- and private-sector clients trust us to solve their most complex challenges. Our teams are driven by a common purpose to deliver a better world through our unrivaled technical and digital expertise, a culture of equity, diversity and inclusion, and a commitment to environmental, social and governance priorities. AECOM is a Fortune 500 firm and its Professional Services business had revenue of $16.1 billion in fiscal year 2025. See how we are delivering sustainable legacies for generations to come at aecom.com and @AECOM.**Freedom to Grow in a World of Opportunity**You will have the flexibility you need to do your best work with hybrid work options. Whether you're working from an AECOM office, remote location or at a client site, you will be working in a dynamic environment where your integrity, entrepreneurial spirit and pioneering mindset are championed.You will help us foster a safe and respectful workplace, where we invite everyone to bring their whole selves to work using their unique talents, backgrounds and expertise to create transformational outcomes for our clients.AECOM provides a wide array of compensation, benefits and well-being programs to meet the diverse needs of our employees and their families. We're the world's trusted global infrastructure firm, and we're in this together - your growth and success are ours too.Join us, and you'll get all the benefits of being a part of a global, publicly traded firm - access to industry-leading technology and thinking and transformational work with big impact and work flexibility. As an Equal Opportunity Employer, we believe in each person's potential, and we'll help you reach yours.We are a Disability Confident Employer and will offer an interview to applicants who have a disability or long-term condition, who meet the minimum/essential criteria for the role. Please let us know using this email address if you would like to apply through the Disability Confident Interview Scheme.All your information will be kept confidential according to EEO guidelines.**ReqID:** J**Business Line:** B&P - Buildings & Places**Business Group:** DCS**Strategic Business Unit:** Europe & India**Career Area:** Engineering**Work Location Model:** HybridPrincipal Fire EngineerGalway, Galway, Ireland**Company Overview**Throughout our worldwide network of experts, clients and communities, we are renowned for our leadership in fire protection engineering - a legacy of responsibility we have proudly upheld since 1939. Today, our expertise extends broadly across closely related security and risk-based fields - from accessibility consulting and risk analysis to process safety, forensic investigations, security risk consulting, emergency management, digital innovation and more.Our engineers and consultants collaborate to solve complex safety and security challenges, ensuring our clients can protect what matters most. For over 80 years, we have helped mitigate risks that threaten lives, property and reputations. Through technology, expertise and industry-leading research, we remain dedicated to our purpose of making our world safe, secure and resilient.At Jensen Hughes, we believe that creating and sustaining a culture of trust, integrity and professional growth starts with putting our people first. Our employees are our greatest strength, and we value the unique perspectives and talents they bring to our organization.Our wide range of Global Employee Networks connect people from across the organization, supporting career development and providing forums for individuals to share experiences on topics they're passionate about. Together, we are cultivating a connected culture where everyone has the opportunity to learn, grow and succeed together.**Job Overview**Jensen Hughes has a rare and exciting opportunity for a talented Principal Fire Engineer to join our Galway team and help us drive excellence across our projects and deliver world-class life safety solutions to our varied client base in 2026. This is a key hire for our ever expanding Galway team. You will not only lead on some of the industry's most exciting projects but also have a key role in shaping the future talent within our teams through mentorship and development opportunities.**Why join us to grow your career?**+ What if I told you 74% of our current Directors/Technical Directors in the UK & Ireland started their career with us as graduates? Exciting right!+ We are the largest fire consultancy in Europe with offices located in Belgium, Finland, Denmark, Italy, and the UK & Ireland. Our reputation for providing innovative, design-focused solutions has made us the consultant of choice for many of Europe's leading property clients.+ As a Principal Fire Engineer you will be an integral part of a dynamic technical team, working with our experienced Engineers alongside other teams including our Forensics division you will work on the industry's leading technical projects.+ Working with us offers an exciting range of opportunities to develop your career within a supportive and diverse team that always strives to do the right thing for our people, clients and communities.+ You will be given early the opportunity to progress rapidly. Jensen Hughes encourages all Engineers to achieve chartered status and offer help and support during the process**Responsibilities**+ You will be responsible for managing large and complex projects to ensure successful delivery to important clients.+ You will have the opportunity to work on a huge portfolio of projects across Ireland, the UK and anywhere in the World, involving all kinds of buildings.+ You will utilise Computational Fluid Dynamics (CFD) modelling and analysis for smoke movement to understand unique environments and propose solutions.+ You will develop and use other forms of Computer Modelling software such as CFAST, Pyrosim and Pathfinder to provide alternative fire engineering solutions.+ You will lead multi-disciplinary teams in addition to mentoring and training graduate engineers.+ You will be client facing and will deal with construction related queries.+ You will support Business Development and finding new clients to help grow the business.**Requirements and Qualifications**+ A background in fire engineering preferably within a consultancy environment.+ A Bachelors degree or higher within Fire Engineering, Mechanical Engineering or similar.+ Ideally be or working towards becoming a Chartered engineer.**Our People Are Our Greatest Asset**At Jensen Hughes, we know that our people are the foundation of our success. To attract and retain the best talent, we offer a competitive and comprehensive benefits package designed to support your wellbeing, work-life balance, and professional growth.**Our UK and Ireland Benefits Include:**+ Private medical insurance+ 33 days paid time off with an additional day after 3 years+ Industry-leading contributory pension scheme+ 4 x life assurance+ Income protection scheme+ Discretionary bonus scheme+ Employee assistance programme+ Enhanced parental-related pay+ Recognition and reward programmes to celebrate team efforts+ Access to extensive technical training and resources**Supporting Your Work-Life Balance**We understand the importance of flexibility and balance. We're happy to discuss hybrid, part-time, and flexible working arrangements to suit both you and the business. We also offer:+ Flexible working hours and patterns including early Friday finish+ Flexible holiday use over Christmas/New Year+ Enhanced holiday entitlement after three years+ The option to carry over up to five unused holiday days into the next year**A Commitment to Continuous Improvement**Our benefits represent a meaningful investment in both our people and the future of Jensen Hughes. We regularly review our benefits programme to ensure it aligns with statutory requirements, market trends, and the needs of our team. Any modifications will be carefully considered to support our employees and the company's long-term goals.\#LI-MR1**_Jensen Hughes is an Equal Opportunity Employer. Qualified candidates will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability or protected veteran status._**At Jensen Hughes, we embrace innovation and understand that people are increasingly using artificial intelligence (AI) tools like ChatGPT and other generative platforms to learn, prepare and communicate. We have provided some guidelines regarding the responsible use of AI in the recruitment process. Please click **here ( to review.The security of your personal data is important to us. Jensen Hughes has implemented reasonable physical, technical, and administrative security standards to protect personal data from loss, misuse, alteration, or destruction. We protect your personal data against unauthorized access, use, or disclosure, using security technologies and procedures, such as encryption and limited access. Only authorized individuals may access your personal data for the purpose for which it was collected, and these individuals receive training about the importance of protecting personal data. Jensen Hughes is committed to compliance with all relevant data privacy laws in all areas where we do business, including, but not limited to, the GDPR and the CCPA. Additionally, our service providers are contractually bound to maintain the confidentiality of personal data and may not use the information for any unauthorized purpose.*Policy on use of 3rd party recruiting agency for direct placementsJensen Hughes will occasionally augment a recruiting search through agencies for certain positions when business conditions warrant. Jensen Hughes will not accept resumes, inquiries or proposals from recruiting agencies as an acceptable method to consider a candidate. 3rd party recruiting agencies must sign a standard Jensen Hughes agreement after being evaluated and accepted by a Human Resources or Talent Acquisition manager, or member of the talent acquisition team. Hiring managers and employees of Jensen Hughes are not authorized to accept resumes, engage in fee-based searches through recruiting firms or sign a search agreement. Please note this policy does not apply to "staffing firms" or firms that are involved with hiring temporary staff. Any recruiting agency interested in being considered may contact our recruiting team at jensenhughesrecruiting.com.Create a Job AlertInterested in building your career at Jensen Hughes? Get future opportunities sent straight to your email.Is this job a match or a miss?Customer Success Manager, Water Engineering UK/I (Remote)**Job Requisition ID #**26WD95594**Position Overview**We are looking for Construction Technology professionals who are passionate about driving digital transformation throughout the construction industry.Reporting to the Manager of Construction Customer Success, you will build lasting and meaningful relationships throughout a portfolio of AEC organisations, specialising in water companies in the UK & Ireland. You will develop and manage the Customer Success Plan and partner with Sales Teams to plan and achieve the expansion of relationships, project adoption and revenue. You will do this through increasing the adoption of the Autodesk Construction Cloud platform and documenting value delivered.**Responsibilities**+ Be accountable for the relationship health of a selected portfolio of accounts+ Develop Customer Success Plans, with documented value delivered+ Improve Autodesk Construction Cloud Adoption within these accounts by solving customer challenges with our technology. Thereby increasing Monthly Active Users, Projects and functionality in use+ Mitigate any churn risk and guide expansion discussions+ Become an expert in our Autodesk Construction Cloud Platform, in current functionality and roadmap**Minimum Qualifications**+ 3+ years experience working for or with Water Companies - (i.e, Digital Lead, BIM Manager, BIM Coordinator, Project Manager, Project Engineer, Quality Manager, specialist contractor)+ Advanced knowledge of AEC workflows and awareness of BIM solutions focused on Construction for the Water Industry+ Advanced Knowledge of ACC ( Autodesk Construction Claud )**Preferred Qualifications**+ 3+ years experience working for or with Water Companies - (i.e, Digital Lead, BIM Manager, BIM Coordinator, Project Manager, Project Engineer, Quality Manager, specialist contractor)+ Advanced knowledge of AEC workflows and awareness of BIM solutions focused on Construction for the Water Industry+ Extremely beneficial would be detailed understanding of technology tools consumed by the water industry such as the ACC Platform or similar CDE and Construction/Project Management solutions+ In-depth knowledge of the construction/con tech industry+ In-depth first hand knowledge of the UK and Ireland water industries+ Proficient in problem solving+ Familiar with the Construction Technology Ecosystem+ Experience communicating the value of technology and its features to customers+ Ability to travel when required+ Experience in building face-to-face relationships with customers**The Ideal Candidate**+ You are passionate about digitisation and progress in the construction industry+ You are comfortable proposing and building processes that will allow our organisation to grow, and collaborate with numerous team members, both internally and externally on site or in the board room+ You have a curious nature to uncover and understand customers challenges, industry trends and required workflows when adopting new technology and recommend best practices to increase and realise return on investment+ Confidence to understand customer business use cases to provide product feedback from customers and contribute to product roadmap discussions+ Excited by technology and happy to get into the product detail**Learn More****About Autodesk**Welcome to Autodesk! Amazing things are created every day with our software - from the greenest buildings and cleanest cars to the smartest factories and biggest hit movies. We help innovators turn their ideas into reality, transforming not only how things are made, but what can be made.We take great pride in our culture here at Autodesk - it's at the core of everything we do. Our culture guides the way we work and treat each other, informs how we connect with customers and partners, and defines how we show up in the world.When you're an Autodesker, you can do meaningful work that helps build a better world designed and made for all. Ready to shape the world and your future? Join us!**Salary transparency**Salary is one part of Autodesk's competitive compensation package. Offers are based on the candidate's experience and geographic location. In addition to base salaries, our compensation package may include annual cash bonuses, commissions for sales roles, stock grants, and a comprehensive benefits package.**Sales Careers**Working in sales at Autodesk allows you to build meaningful relationships with customers while growing your career. Join us and help make a better, more sustainable world. Learn more here: & Belonging**We take pride in cultivating a culture of belonging where everyone can thrive. Learn more here: you an existing contractor or consultant with Autodesk?**Please search for open jobs and apply internally (not on this external site).Is this job a match or a miss?Be The First To KnowAbout the latest Principal r d engineer crdn Jobsin Galway !Set Email Alert:Job titleLocationSenior QA Specialist, Biologics Drug Substance (Remote / Home Based)If you are a current Jazz employee please apply via the Internal Career site.Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to developing life-changing medicines for people with serious diseases — often with limited or no therapeutic options. We have a diverse portfolio of marketed medicines, including leading therapies for sleep disorders and epilepsy, and a growing portfolio of cancer treatments. Our patient-focused and science-driven approach powers pioneering research and development advancements across our robust pipeline of innovative therapeutics in oncology and neuroscience. Jazz is headquartered in Dublin, Ireland with research and development laboratories, manufacturing facilities and employees in multiple countries committed to serving patients worldwide. Please visit for more information.The Biologics Drug Substance Senior Quality Assurance Specialist is Responsible for performing key Quality tasks in respect of Company Biologics products. Work in the External Manufacturing Quality Group within the Technical Operations department, which oversees contract manufacturing operations, as well as Internal Quality Systems. Reporting directly to the Drug Substance Lead, External Manufacturing QA.Essential Functions/ResponsibilitiesThe position is responsible for monitoring and supporting the quality performance of contract manufacturing organisations and material suppliers to all applicable GXP standards. Responsible for, but not limited to:Monitoring the daily operations at the Contract Manufacturer, performing batch review and disposition, reviewing and approving product complaints, deviations, Validation protocols, change controls and leading product related investigations.CMO Batch file and product testing record review and approval. Associated lot Disposition activity.Ensuring compliance of all respective contract manufacturers to both internal Jazz requirements and country specific regulationsCollaboration with all contract manufacturers, packagers and testing laboratories to resolve any quality issues.Contributing to the successful outcome of all regulatory inspections associated with company business, both internally and at contract manufacturers, as required.Highlighting any risks associated with maintaining supply of commercial drug products to all markets.Conducting vendor audits and vendor site visits as required.Assisting in internal audits and regulatory agency inspections.Summarizing CMO Annual Product Quality Reviews and supporting regulatory submissionsAssist with the generation of Jazz APQR (Annual Product Quality Review).Maintaining product related Quality Technical Agreements (QTAs).Understanding new regulations and guidelines, as they apply to the company business and implement systems and procedures to incorporate these new regulations as appropriate.Review and approve moderate complexity deviations and associated corrective actions.Support the generation of new, as well as improvement of, existing department SOPs.Support delivery of projects.Work with management to resolve project issues and resource constraints within the team.Liaise with the internal and external stakeholders to resolve and clarify any point of issue.Review and approve less complex validation documents.Partner with other departments/groups to problem-solve and address moderately complex issues.Collaborate in the continuous improvement of the QA processes, identifying opportunities and leading them up to the implementation.Represent QA in cross-functional project teams for moderately difficult projects.Participate in and facilitate regulatory inspection readiness.Coordinates and collaborates with other teams to meet organizational goals and work requirements.Receives assignments in the form of objectives and determines how to use resources to meet schedules and goals.Follows processes and operational policies in selecting methods and techniques for obtaining solutions; solves moderately complex problems and can identify viable and often innovative options.Uses analytical skills and judgment to recommend the "best" solution.Demonstrates success using compliance knowledge, creativity, and regulatory perspectives to solve problems, especially those associated with major and critical deviations.Maintain quality from cell banking through to production and post-release events (e.g., stability, product complaints).Required Knowledge, Skills, and AbilitiesStrong knowledge of GMP and Regulatory Compliance as applicable to the Pharmaceutical/ Biotechnology Industry.Ability to understand and apply GMP regulations as they relate to manufacturing, QC analytical testing, and facility operations, deep knowledge of Biologics manufacturing.Substantial experience working in or directly supporting manufacturing within a biologics drug substance manufacturing site.Experience with contract manufacturing is desirable.Significant experience (>5years) of commercial and/or late state clinical phase GMP manufacturing of biologics.Highly organised, with exceptional time management and prioritization.Excellent verbal and written communication skills.Experience in Drug Product Manufacture in addition to Drug Substance an advantageQP eligibility or progress toward QP certification is highly desirable.Required/Preferred Education and LicensesBachelor’s degree in pharmacy, chemistry, biotechnology, biochemistry, microbiology or a related disciplineJazz Pharmaceuticals is an equal opportunity/affirmative action 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 characteristic protected by law.The successful candidate will also be eligible to participate in various benefits offerings, including, but not limited to, medical, dental and vision insurance, retirement savings plan, and flexible paid vacation. For more information on our Benefits offerings please click here: .If you are a current Jazz employee please apply via the Internal Career site.Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to developing life-changing medicines for people with serious diseases — often with limited or no therapeutic options. We have a diverse portfolio of marketed medicines, including leading therapies for sleep disorders and epilepsy, and a growing portfolio of cancer treatments. Our patient-focused and science-driven approach powers pioneering research and development advancements across our robust pipeline of innovative therapeutics in oncology and neuroscience. Jazz is headquartered in Dublin, Ireland with research and development laboratories, manufacturing facilities and employees in multiple countries committed to serving patients worldwide. Please visit for more information.The Biologics Drug Substance Senior Quality Assurance Specialist is Responsible for performing key Quality tasks in respect of Company Biologics products. Work in the External Manufacturing Quality Group within the Technical Operations department, which oversees contract manufacturing operations, as well as Internal Quality Systems. Reporting directly to the Drug Substance Lead, External Manufacturing QA.Essential Functions/ResponsibilitiesThe position is responsible for monitoring and supporting the quality performance of contract manufacturing organisations and material suppliers to all applicable GXP standards. Responsible for, but not limited to:Monitoring the daily operations at the Contract Manufacturer, performing batch review and disposition, reviewing and approving product complaints, deviations, Validation protocols, change controls and leading product related investigations.CMO Batch file and product testing record review and approval. Associated lot Disposition activity.Ensuring compliance of all respective contract manufacturers to both internal Jazz requirements and country specific regulationsCollaboration with all contract manufacturers, packagers and testing laboratories to resolve any quality issues.Contributing to the successful outcome of all regulatory inspections associated with company business, both internally and at contract manufacturers, as required.Highlighting any risks associated with maintaining supply of commercial drug products to all markets.Conducting vendor audits and vendor site visits as required.Assisting in internal audits and regulatory agency inspections.Summarizing CMO Annual Product Quality Reviews and supporting regulatory submissionsAssist with the generation of Jazz APQR (Annual Product Quality Review).Maintaining product related Quality Technical Agreements (QTAs).Understanding new regulations and guidelines, as they apply to the company business and implement systems and procedures to incorporate these new regulations as appropriate.Review and approve moderate complexity deviations and associated corrective actions.Support the generation of new, as well as improvement of, existing department SOPs.Support delivery of projects.Work with management to resolve project issues and resource constraints within the team.Liaise with the internal and external stakeholders to resolve and clarify any point of issue.Review and approve less complex validation documents.Partner with other departments/groups to problem-solve and address moderately complex issues.Collaborate in the continuous improvement of the QA processes, identifying opportunities and leading them up to the implementation.Represent QA in cross-functional project teams for moderately difficult projects.Participate in and facilitate regulatory inspection readiness.Coordinates and collaborates with other teams to meet organizational goals and work requirements.Receives assignments in the form of objectives and determines how to use resources to meet schedules and goals.Follows processes and operational policies in selecting methods and techniques for obtaining solutions; solves moderately complex problems and can identify viable and often innovative options.Uses analytical skills and judgment to recommend the "best" solution.Demonstrates success using compliance knowledge, creativity, and regulatory perspectives to solve problems, especially those associated with major and critical deviations.Maintain quality from cell banking through to production and post-release events (e.g., stability, product complaints).Required Knowledge, Skills, and AbilitiesStrong knowledge of GMP and Regulatory Compliance as applicable to the Pharmaceutical/ Biotechnology Industry.Ability to understand and apply GMP regulations as they relate to manufacturing, QC analytical testing, and facility operations, deep knowledge of Biologics manufacturing.Substantial experience working in or directly supporting manufacturing within a biologics drug substance manufacturing site.Experience with contract manufacturing is desirable.Significant experience (>5years) of commercial and/or late state clinical phase GMP manufacturing of biologics.Highly organised, with exceptional time management and prioritization.Excellent verbal and written communication skills.Experience in Drug Product Manufacture in addition to Drug Substance an advantageQP eligibility or progress toward QP certification is highly desirable.Required/Preferred Education and LicensesBachelor’s degree in pharmacy, chemistry, biotechnology, biochemistry, microbiology or a related disciplineJazz Pharmaceuticals is an equal opportunity/affirmative action 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 characteristic protected by law.The
#J-18808-Ljbffr