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Client: Johnson and Johnson
Location: Galway, Ireland
Job Category: Other
EU work permit required: Yes
Job Reference: 5b4382acb1d0
Job Views: 1
Posted:
Expiry Date:
Job Description: At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow and profoundly impact health for humanity.
Learn more at
Job Function: R&D Product Development
Job Sub Function: Biomedical Engineering
Job Category: Scientific/Technology
All Job Posting Locations: Galway, Ireland
Job Description: We are searching for the best talent for a Senior R&D Engineer to be in Galway, Ireland.
About MedTech: Fueled by innovation at the intersection of biology and technology, we're developing the next generation of smarter, less invasive, more personalized treatments.
Your unique talents will help patients on their journey to wellness.
Learn more at
About Cerenovus: CERENOVUS, part of Johnson & Johnson Medical Devices Companies, is a global leader in neurovascular care.
Our commitment to changing the trajectory of stroke is inspired by our long heritage and dedication to helping physicians protect people from a lifetime of hardship.
CERENOVUS offers a broad portfolio of devices used in the endovascular treatment of hemorrhagic and ischemic stroke.
What is it like to work at CERENOVUS Galway?
We prioritize quality, compliance, and ethics, and are committed to understanding clot science through our Neuro Thromboembolic Initiative (NTI).
We invest in our people, support diversity, and foster innovation through employee resource groups.
Purpose of role: The Senior R&D Engineer supports managing and delivering complex acute ischemic stroke projects with significant technical challenges.
Responsibilities include process development, design development, implementation of new equipment/automation, and new product introduction.
Key duties involve understanding disease states, translating needs into specifications, managing teams, developing prototypes, creating detailed drawings, selecting materials, developing project plans, liaising with external resources, managing risks, writing procedures, and developing training and marketing materials.
Essential requirements include an Honours degree in Mechanical or Biomedical Engineering or equivalent, experience in all stages of medical device design and development, strong engineering knowledge, data review skills, and excellent communication skills.
Desirable qualities include results-driven attitude, interpersonal skills, motivation, and specific experience with medical devices, cardiovascular, or neurovascular implants or instruments.
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