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Senior Clinical R&D Engineer

  • Salary: £60000 - £70000 per annum per year
  • Job Type:Permanent

Posted 21 days ago

  • Sector: Medical Technology
  • Contact: Benji Delaney
  • Contact Email: b.delaney@sciproglobal.com
  • Expiry Date: 08 February 2023
  • Job Ref: 208354_1673274712

I have partnered with an industry leading Medical Device company on their search for a Senior Clinical R&D Engineer and think, with your experience, you would be an excellent fit!

Location: Dublin, Ireland

This role offers you the opportunity to play a pivotal role within the R&D Team, focusing on the development of a Best-In-Class minimally invasive structural heart device; within an award winning and European and US VC backed Medical Device Company.

Responsibilities:
* Responsible for screening of patients as part of the DUO device clinical studies
* Using knowledge of the device, right heart anatomy, physiology and pathology, process patient echocardiography exams and CT scans using DICOM and CT analysis software (Mimics) to make recommendations for patient inclusion in clinical studies
* Complete analysis of patient follow up data and summarise this into reports on product performance, safety and efficacy.
* Make recommendations on design iterations and updates for existing and future designs using knowledge developed from patient screening and follow up, as well as anatomical analysis of patient CTs.
* Working with a cross functional team, develop and maintain physician training and educational materials.
* Provide hands on case support in the form of delivery of training materials to physicians, preparation of the device in the cath lab and physician proctoring during cases.
* Provide R&D expertise to lead investigations into procedural complaints as they may arise.
* Using the knowledge and insight gained from the clinical environment, develop test methods for product evaluation and validation. Develop and execute test method validations.
* Provide technical and project leadership for R&D activities as required.
* Leverage and liaise with external resources to achieve project goals.
* Lead user related risk management activities and act as subject matter expert for inputs to other risk management efforts as it pertains to the device design and clinical use.
* Ensure quality in the product's design for durability, usability, reliability, functionality, marketability, and manufacturability

If you would like to hear more about this role, contact me on:
02039295872
b.delaney@sciproglobal.com