What Principal Biomedical Electronics Engineer...Showing 3 Principal Biomedical Electronics Engineer Crdn jobs in GalwayPrincipal 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?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?Senior 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 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: .Is this job a match or a miss?Be The First To KnowAbout the latest Principal biomedical electronics engineer crdn Jobsin Galway !Set Email Alert:Job titleLocationWhat other jobs are popular in this category?Explore these high-demand roles to expand your search:Didn't find the right job? Get Career Advice to find your ideal role.
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