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Senior Research and Development Engineer

Overview

The purpose of this role is to work as part of the Research and Development team in the design, development and taking to market of medical devices for the Cook Medical.

 

Reporting to: Team Lead, Research and Development / Manager, Research and Development  

 

 

Find out more about Cook Medical here

Responsibilities

  • Perform Duties of Senior Research and Development Engineer:
    • Design development
      • Prototyping and test method design.
      • Design and/or process evaluation, reviews, specifications, verification and validation, protocols and reports and transfer to production activities in a timely and effective manner.
    • Product and project risk analysis and risk management.
    • Develop prototypes which are consistent with the clinical and design requirements of the project.
    • Research new therapies and design solutions to develop and complement the existing product portfolio.
    • Introduce new equipment, materials and technologies.
    • Generation of Design History File documentation.
    • Support of regulatory submissions.
  • Work closely with Key Opinion Leaders (KOL’s), physicians and product managers to develop innovative medical devices to improve patient care.
  • Project lead for assigned Research and Development team/s including technical and project management leadership responsibly.
    • Lead technical development of projects.
    • Lead all key design decisions to ensure quality design selection.
    • Manage the activities of the project team and drive project tasks to ensure timely completion of project milestones and business metrics are achieved.
    • Work closely to build effective relationships with cross functional groups to achieve project and company goals.
    • Retrospective project reviews to understand lessons learned.
    • Manage device evaluations.
    • Compliance with Quality, Regulatory and company policies and systems.
  • Mentoring, coaching and development of team members if required.
    • Foster innovation and creativity within team and perform disclosure reviews.
  • Ensure compliance with Quality, Regulatory and company policies and systems.
  • Communications:
    • Regular communication to cross-functional teams, senior management and business unit leaders.
    • Project status communications and reporting.
  • Remain on the forefront of emerging industry practices.
  • Instrumental in driving and implementing change to improve departmental and company performance.
  • Educating oneself in the medical area for which the new devices are being developed in order to have an appreciation for what needs to be achieved with these products.
  • Support other cross functional groups to deliver company goals.
  • Act as a designee for the Manager, Research and Development or Team Lead, Research and Development.
  • Ensure that Cook’s Code of Conduct is considered in all business matters carried out on Cook’s behalf.

 

Qualifications

  • Bachelor’s degree required, preferably in engineering or a related field.
  • Minimum of 5 years’ relevant experience is required.
  • Experience in Product Development projects within Medical Device or regulated industry/adjacent experience.
  • Proven project/technical experience.
  • Project management methodology and skills.
  • Proven experience working closely with project managers.
  • Knowledge of medical device quality standards ISO13485/FDA practices, EUMDR, GMP and similar regulated industry standards.
  • Strong statistical understanding and experience e.g. DOE and/or Gage R&R. 
  • Strong technical writer.
  • Good working knowledge of Solidworks and/or Pro Engineer CAD.
  • Experience of medical device development from concept through to commercialisation.
  • Ability to effectively translate needs of clinicians and Strategic Business Unit into project inputs.
  • Willingness and availability to travel on company business.

 

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. 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 

 

#LI-Hybrid

##IrishJobs

Average salary estimate

$90000 / YEARLY (est.)
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$80000K
$100000K

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What You Should Know About Senior Research and Development Engineer, Cook Group

As a Senior Research and Development Engineer at Cook Medical in Limerick, you'll be an integral part of our dynamic R&D team, where innovation meets patient care. Your primary focus will be on designing, developing, and bringing to market cutting-edge medical devices. You'll dive into a variety of exciting responsibilities, including prototyping, test method design, and rigorous product evaluations. You're not just a facilitator; you're a project lead, guiding your team towards timely project milestones while ensuring every detail adheres to the highest standards of quality and regulatory compliance. Collaboration is key in your role: you'll interact with Key Opinion Leaders and medical professionals to understand their needs and translate them into practical design solutions. Your expertise in medical device development, especially in regulated industries, will come into play as you introduce new technologies and materials that enhance our product portfolio. With your strong technical skills, you'll generate thorough documentation for design processes and improve project efficiency. At Cook Medical, we value creativity and innovation, and your mentorship will help develop team members' skills, ensuring we continuously push the boundaries of what's possible. Limerick is not just where you work; it's a vibrant hub for our R&D efforts, giving you the chance to make a real impact on healthcare systems worldwide. Join us in turning ideas into reality and improving patient lives through technology you help create.

Frequently Asked Questions (FAQs) for Senior Research and Development Engineer Role at Cook Group
What are the main responsibilities of a Senior Research and Development Engineer at Cook Medical?

The Senior Research and Development Engineer at Cook Medical is responsible for a range of tasks including designing and developing innovative medical devices, conducting prototyping and testing, managing project timelines, and ensuring compliance with quality standards. This role also involves collaborating with medical professionals to align product features with clinical needs, leading project teams, and generating documentation critical for regulatory submissions.

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What qualifications do I need to become a Senior Research and Development Engineer at Cook Medical?

To qualify for the Senior Research and Development Engineer position at Cook Medical, candidates should have a Bachelor's degree in engineering or a related field, along with a minimum of five years of relevant experience in product development within the medical device sector. Familiarity with project management methodologies, ISO standards, and medical device quality practices is also essential for success in this role.

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How does Cook Medical ensure the quality of its medical devices in the R&D process?

Cook Medical places a strong emphasis on quality during the R&D process through rigorous evaluations, risk management analysis, and adherence to regulatory standards like ISO13485 and FDA practices. The Senior Research and Development Engineer is responsible for leading risk assessments, ensuring that the design and development processes meet strict quality criteria before moving devices to production.

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What kind of technologies and materials will I be working with at Cook Medical?

As a Senior Research and Development Engineer at Cook Medical, you will be introduced to a variety of cutting-edge technologies and materials that are used in the development of medical devices. This includes working with advanced materials suited for medical applications and utilizing innovative technologies that enhance the efficacy and safety of our products.

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Why is collaboration important for a Senior Research and Development Engineer at Cook Medical in Limerick?

Collaboration is crucial for a Senior Research and Development Engineer at Cook Medical as it fosters the exchange of ideas between engineering teams and healthcare professionals. This collaborative environment allows engineers to incorporate clinical insights into product design, ensuring that the devices developed truly meet the needs of patients and medical practitioners.

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Common Interview Questions for Senior Research and Development Engineer
Can you describe your experience with medical device development from concept to commercialization?

In addressing this question, it's essential to detail specific projects you've worked on, emphasizing your role throughout varying phases—from ideation through to market launch. Discuss how you addressed regulatory requirements and collaborated with cross-functional teams to ensure success.

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What methodologies do you use for risk management in product development?

Detailing a systematic approach to risk management is key in your response. Talk about specific tools like FMEA (Failure Mode and Effects Analysis) and how you incorporate risk assessments at different stages of product development to mitigate potential issues effectively.

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How do you ensure effective communication within cross-functional teams?

Highlight your strategies for maintaining clear and open channels of communication. Mention tools you utilize for collaboration and how regular updates and feedback loops contribute to project success, ensuring everyone is aligned with project goals.

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Describe a challenging project you led and how you managed it.

In your response, focus on a specific project that faced difficulties, discussing the challenges encountered, the strategies you employed to overcome them, and highlighting your leadership and problem-solving skills that ensured project delivery.

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What techniques do you use for prototype development and testing?

Discuss the importance of both rapid prototyping and rigorous testing protocols. Share any specific technologies or software you use, and how you gather feedback to refine prototypes in alignment with clinical requirements.

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How do you incorporate feedback from Key Opinion Leaders into your product designs?

Emphasize the importance of active listening and constructive dialogue. Explain how you gather insights from KOLs, integrate their feedback into the design process, and the impact this collaboration has on product efficacy and market acceptance.

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What statistical methods are you familiar with regarding medical device development?

Talk about your experience with various statistical methods such as Design of Experiments (DOE) and Gage Repeatability and Reproducibility (Gage R&R). Explain how these methodologies help in validating product designs and ensuring consistency in quality.

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How do you stay updated with emerging technologies in the medical device industry?

Discuss your commitment to continuous learning through industry conferences, workshops, and relevant literature. Mention specific sources or networks you engage with to gain insights on technological advancements impacting medical devices.

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Have you ever faced a compliance issue in a project? How did you handle it?

Describe a specific instance where compliance was challenged, detailing how you identified the issue, the steps you took to address it, and the outcomes that resulted from your intervention.

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What role does documentation play in your project management process?

Explain the critical nature of documentation in ensuring transparency and regulatory compliance. Discuss how you maintain detailed records throughout the development process and how this documentation supports both product development and compliance.

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DATE POSTED
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