Sr R&D Engineer

Overview

Sr R&D Engineer - Johnson & Johnson MedTech | Neurovascular

We are searching for the best talent for a Sr R&D Engineer to be in Galway, Ireland.

Location: Ballybrit, Galway (office based 2-3 days per week)

Reports to: R&D Project Manager

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 https://www.jnj.com/medtech

J&J MedTech Neurovascular (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. J&J MedTech Neurovascular offers a broad portfolio of devices used in the endovascular treatment of hemorrhagic and ischemic stroke.

Role Purpose

J&J MedTech Neurovascular a Johnson & Johnson company is recruiting for a Senior Research and Development Engineer located in Galway Ireland.

The role of Senior R&D Engineer I supports managing and delivering complex acute ischemic stroke projects with significant technical challenges. Overall responsibility for various aspects of new development projects, including process development, design development, implementation of new equipment/automation and new product introduction.

What it's like to work at J&J MedTech Neurovascular Galway

J&J MedTech Neurovascular Galway is part of a global leader in neurovascular care, focused on innovation and improving patient outcomes while fostering a diverse and inclusive work environment.

Responsibilities

• Develop an understanding of the disease state, gather user needs, and translate into technical specifications.
• Support the management of the direct team to deliver on performance, time and cost targets.
• Generate creative product solutions to address unmet needs.
• Develop test models for prototype performance evaluations.
• Build and test prototypes; analyse test data and interpret to identify optimal solution(s).
• Create detailed component and finished device assembly drawings/specifications.
• Identify and select product materials, assembly methods and define process settings.
• Develop and deliver project plans to performance, time and cost targets.
• Leverage and liaise with external resources to achieve project goals.
• Identify and manage key risks throughout the product lifecycle.
• Write procedures, protocols, specifications, and reports.
• Evaluate and assess physician (user) techniques and develop product training materials.
• Support developing marketing materials (presentations/videos/demos).
• Other duties as assigned or required.

Essential requirements

• Honours degree in Mechanical or Biomedical Engineering or equivalent.
• A minimum of 4 years' experience in all stages of medical device design and development (including design with SolidWorks, product lifecycle data management systems, prototyping, and testing).
• Strong design and technical ability based on a broad and deep knowledge of fundamental engineering principles.
• Data review and statistical methods skills (Minitab).
• Strong work ethic, creative problem solving, capable of working on own initiative.
• Excellent writing, presentation, and verbal communication skills essential.

Desirable

• Results and deadline driven with an ability to handle multiple tasks and operate in a fast-paced environment.
• Excellent interpersonal skills and ability to work with people to achieve results.
• Highly motivated and an enthusiastic self-starter with the ability to work under own initiative and as a team player.
• Specific experience on Medical Devices, cardiovascular or neurovascular implants or instruments.

Seniority level

• Not Applicable

Employment type

• Full-time

Job function

• Engineering and Information Technology

Industries

• Hospitals and Health Care

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