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Research and Development Engineer 2Confidential • Limerick, Wexford, Ireland
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Confidential

Research and Development Engineer 2

Confidential
  • IE
    Limerick, Wexford, Ireland
  • IE
    Limerick, Wexford, Ireland
Jetzt Bewerben

Über

Why Join Us About Cook Limerick Cook Medical has been in Limerick since 1996, starting out with labeling and distribution and steadily growing and evolving to include manufacturing, centralised customer support and on to collaborative product development in the Innovation Centre.
Find out if this opportunity is a good fit by reading all of the information that follows below.
The Ireland location is our European headquarters and houses our EMEA Support Centre.
This location currently employs more than 1000 people and manufactures 10% of Cook's products for global markets.
Research and Development in Limerick Our mission with R&D is to invent, manufacture, and deliver a unique portfolio of medical devices to the healthcare systems of the world.
Our R&D team in Limerick is split into two divisions, Vascular and Medsurg.
The R&D engineering teams are responsible for bringing a product from idea or concept all the way to market launch.
The R&D Vascular division in Limerick has two programs, peripheral arterial disease (PAD) and venous therapies.
The R&D engineers have the opportunity to create novel ideas within feasibility, learn and meet the requirements to bring a medical device through verification and validation, generation of a design history file and be a part of bringing a new product onto the market.
All this is done through collaboration within small or large R&D teams and working with cross functional teams both locally in Limerick and globally with our sister companies.
Our employee benefits include: Hybrid Work Model Company sponsored Defined Contribution pension scheme Medical Health Insurance cover for you and your immediate family Life Assurance and Income Protection cover Educational Assistance Performance related Bonus Extensive health & wellness program including Indian head massages, healthy lifestyle seminars, mindfulness courses, physio sessions, flu vaccinations, nutrition talks Fully equipped gym on site 39-hour week with flexible start & finish times Paid time off to participate in volunteer activities Free parking Subsidised restaurant Sports & Social club Overview The Research and Development Engineer 2 will be a technical leader and/or growing subject matter expert, applying engineering principles to solve technical challenges and ensuring products meet clinical needs, safety requirements, and quality standards.
In this role, they may have the following responsibilities: Lead portions of projects/programs while also supporting other project teams, as needed.
Collaborate across functional department(s), grow and advance their area of technical expertise, and provide guidance and technical leadership within their area.
Contribute to the development of best practices in focus area(s) of work.
Responsibilities li" data-ccp-parastyle-defn="{"ObjectId":"8d7a56e0-a7b7-54f4-afb6a82|1","ClassId":,"Properties":[,"Times New Roman",,"Times New Roman",,"Times New Roman",,"Times New Roman",,"Times New Roman",,"ul > li",,"true",,"ulli",,"Normal"]}">Continue to perform the functions, duties, and expectations of the Research and Development Engineer 1 at a high level, as applicable.
li">Responsibilities for supporting technical leadership may include: li">Leading technical development for portions of projects/programs.
li">Support key design decisions to ensure quality of design selection to meet customer needs.
li">Attainment of goals within area of expertise.
li">Responsibilities for providing subject matter expertise may include: li">Work within project/program team(s) to identify and agree on focus area(s) for their projects across the functional department(s).
li">Conduct research and contribute to the development of best practices in focus area(s).
li">Support and contribute to the creation of procedures or white paper guidance for functional groups.
li">Deploy knowledge and support the correct implementation of new concepts and/or approaches.
li">Interact with SME's, physicians, and product managers to develop innovative medical devices to improve patient care, as applicable.
li">Assumes li">responsibility li">in interpreting data, organizing, executing, and coordinating project activities within portions of projects/programs.
li">Develop and execute activities and documentation to create and maintain design history files.
li">Assists with the development and implementation of new processes and solutions that will impact the achievement of the department business metrics.
li">Utilize and implement engineering knowledge and technical expertise to support the department.
li">Provide technical input on company intellectual property relevant to area of work to drive innovation and IP generation.
li">Assist with innovative and creative problem-solving techniques to develop and implement cutting edge medical devices and technologies, overcoming complex engineering challenges and driving product/process excellence to support projects/programs within the department.
li">Collaborate, communicate, and manage effective relationships with cross functional groups to support the achievement of project milestones.
li">Learn the organization's business processes and systems, as applicable to your duties and responsibilities.
li">Comply with Quality, Regulatory, and company policies and systems.
Qualifications li" data-ccp-parastyle-defn="{"ObjectId":"8d7a56e0-a7b7-54f4-afb6a82|1","ClassId":,"Properties":[,"Times New Roman",,"Times New Roman",,"Times New Roman",,"Times New Roman",,"Times New Roman",,"ul > li",,"true",,"ulli",,"Normal"]}">Bachelor's degree in Engineering and 3 years' relevant experience li"> required li">.
Relevant advanced degrees ( li">Master's li"> or PhD) may reduce the experience requirement by 2-4 years.
li">Experience in a technical role within Medical Device or regulated industry/adjacent experience.
Vascular delivery systems, stents or stent grafts would be an advantage.
li">Min 2-3 years solid experience generating DHF documentation (risk management, design inputs, design standards, test protocols & reports) for Class III medical devices.
li">Experience in sterilisation animal studies, microbiology and biocompatibility would be an advantage.
li" data-ccp-parastyle-defn="{"ObjectId":"8d7a56e0-a7b7-54f4-afb6a82|1","ClassId":,"Properties":[,"Times New Roman",,"Times New Roman",,"Times New Roman",,"Times New Roman",,"Times New Roman",,"ul > li",,"true",,"ulli",,"Normal"]}">Strong analytical and critical thinking skills.
li" data-ccp-parastyle-defn="{"ObjectId":"8d7a56e0-a7b7-54f4-afb6a82|1","ClassId":,"Properties":[,"Times New Roman",,"Times New Roman",,"Times New Roman",,"Times New Roman",,"Times New Roman",,"ul > li",,"true",,"ulli",,"Normal"]}">Strong technical writing.
li">Ability to work with cross functional teams to solve complex problems.
li">Knowledge of relevant ISO, EU, FDA medical devices standards regulations is preferred.
li">This role requires fluency in Artificial Intelligence (AI) and data concepts, including the ability to critically evaluate AI li">outputs li">, improve workflows using approved tools, identify and mitigate bias or inaccuracies, and communicate AI-driven insights clearly and responsibly to peers and managers.
Must be able to perform the essential functions of the job, subject to reasonable accommodation requirements, as applicable by local, regional, or national law or regulation.
li" data-ccp-parastyle-defn="{"ObjectId":"8d7a56e0-a7b7-54f4-afb6a82|1","ClassId":,"Properties":[,"Times New Roman",,"Times New Roman",,"Times New Roman",,"Times New Roman",,"Times New Roman",,"ul > li",,"true",,"ulli",,"Normal"]}">Work under general office environmental conditions li">Sitting for extended li">periods, li"> utilizes close visual acuity for working with computers, etc., li" data-ccp-parastyle-defn="{"ObjectId":"8d7a56e0-a7b7-54f4-afb6a82|1","ClassId":,"Properties":[,"Times New Roman",,"Times New Roman",,"Times New Roman",,"Times New Roman",,"Times New Roman",,"ul > li",,"true",,"ulli",,"Normal"]}">In line with local health and safety requirements, personal protective equipment may be required in areas associated with this position.
li">May require occasional travel.
Each employee must acknowledge and agree to comply with all written company policies, procedures, and standards, including without limitation the Employee Manual/Handbook (local, regional, and, if applicable, company-specific), Code of Conduct (Cook Medical and Cook Group), Electronic Information Policy, HIPAA regulations, and any Non-Competition and Confidentiality Agreement.
#LI-AK1 To be considered for this role you will be redirected to and must complete the application process on our careers page. xyswxtq
To start the process click the Continue to Application or Login/Register to apply button below.
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  • Limerick, Wexford, Ireland

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  • English
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