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R&D Engineer

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Veryan Medical

2mo ago

  • Job
    Full-time
    Junior Level
  • Research & Development
    Engineering
  • Galway
  • Quick Apply

AI generated summary

  • You must have a degree in Engineering or related field, 1+ years in medical device R&D, knowledge of ISO13485/FDA standards, strong communication skills, and experience in design/testing.
  • You will design and develop products, conduct testing, ensure compliance with regulations, manage project documentation, and collaborate with QA and project teams while applying problem-solving techniques.

Requirements

  • Perform project tasks ensuring adherence to the company’s procedures which have been developed in compliance with ISO13485, the Medical Device Directives and FDA 21 CFR 820
  • To provide design, development and technical input to the Company’s development projects.
  • Packaging development, including design and testing required for new and existing products under development.
  • Test method Development, document, training, and validation.
  • Support the development of manufacturing processes using tools such as design for six sigma (DFSS) and design for manufacturing (DFM).
  • Summarise in vitro test data and communicate the results to project teams leaders and functional groups. Demonstrate a working knowledge of concepts & applications in mechanical and process engineering.
  • Using the principles of systematic problem solving, learn and execute analytical techniques such as DOE, Six sigma and statistics.
  • Work with the QA Department in developing test, verification and validation (including design review) procedures.
  • Manage and co-ordinate procedures, protocols, reports and purchases relevant to the R&D tasks assigned to you, keeping the R&D Project Manager updated.
  • Bachelor’s/Master’s degree in Engineering or local equivalent in a scientific discipline and/or appropriate experience.
  • Good communication and interpersonal skills.
  • Ability to prioritise project tasks and meet deadlines.
  • Minimum of one year experience working as an R&D Engineer in the medical device industry.
  • Good knowledge of biomechanics and mechanical analysis & design.
  • Strong communication skills both written and verbal.

Responsibilities

  • Perform project tasks ensuring adherence to the company’s procedures which have been developed in compliance with ISO13485, the Medical Device Directives and FDA 21 CFR 820
  • To provide design, development and technical input to the Company’s development projects.
  • Packaging development, including design and testing required for new and existing products under development.
  • Test method Development, document, training, and validation.
  • Support the development of manufacturing processes using tools such as design for six sigma (DFSS) and design for manufacturing (DFM).
  • Summarise in vitro test data and communicate the results to project teams leaders and functional groups. Demonstrate a working knowledge of concepts & applications in mechanical and process engineering.
  • Using the principles of systematic problem solving, learn and execute analytical techniques such as DOE, Six sigma and statistics.
  • Work with the QA Department in developing test, verification and validation (including design review) procedures.
  • Manage and co-ordinate procedures, protocols, reports and purchases relevant to the R&D tasks assigned to you, keeping the R&D Project Manager updated.
  • Other duties as required by the Company.

FAQs

What is the job title for this position?

The job title is R&D Engineer.

Where is the job located?

The job is located in Galway and offers a hybrid working option.

What type of employment is offered for this position?

This position is full-time and permanent.

What qualifications are required for this role?

A Bachelor’s or Master’s degree in Engineering or a local equivalent in a scientific discipline is required, along with appropriate experience.

How much experience is needed to apply for this R&D Engineer role?

A minimum of one year of experience working as an R&D Engineer in the medical device industry is required.

What are the key responsibilities of the R&D Engineer?

Key responsibilities include providing design and technical input to development projects, packaging development, test method development, and supporting manufacturing process development among other tasks.

What skills are important for the R&D Engineer position?

Important skills include good knowledge of biomechanics and mechanical analysis, strong communication skills, and the ability to prioritize project tasks and meet deadlines.

What are some benefits of working with Veryan Medical?

Benefits include a competitive salary and bonus, pension scheme, private medical insurance, paid sick leave, annual leave, flexible working hours, and opportunities for further education and training.

What are the company values at Veryan Medical?

The company values are collaborative, innovative, empowering, patient-centric, and acting with integrity.

How does Veryan Medical handle applicant data?

Veryan Medical retains applicant details for the duration necessary to process applications, ensuring compliance with data protections under legal frameworks. Applicants have rights regarding their data which can be reviewed under their recruitment privacy notice.

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Veryan Medical

Science & Healthcare
Industry
51-200
Employees
2003
Founded Year

Mission & Purpose

Veryan has developed innovative technology to improve the performance of vascular stents by adopting the principle of biomimicry; developing structures that imitate those occurring naturally. Veryan’s vascular biomimetic stent technology involves adapting a straight stent design to a three-dimensional helical shape, which more closely mimics the natural geometry of the human vascular system. The BioMimics 3D stent belongs to a new generation of self-expanding stent design with advanced biomechanical and flow performance properties, creating the potential to transform the treatment of patients with symptomatic peripheral arterial disease of the lower limbs. This highly differentiated technology has been clinically proven in a multicentre, randomised clinical trial (the Mimics study) in superficial femoral and proximal popliteal (femoropopliteral) arteries of the leg and received CE Mark approval in November 2012. Veryan was formed in 2003 as the result of a technology spin out from Imperial College, London, UK. Veryan has designed, patented and developed a highly innovative three dimensional (3D) Nitinol (nickel-titanium alloy) stent technology – BioMimics 3D – based on the pioneering work by Professor Colin Caro (Emeritus Professor of Physiological Mechanics, Dept. of Bioengineering, Imperial College London) on the link between vessel geometry, blood flow mechanics and vascular disease.1 Veryan benefits from a highly experienced Board of Directors and the Company’s management team has built an outstanding development group, supported by a world class Scientific Advisory Board. The Company’s head office is in Horsham, West Sussex, UK, and the research and development facility is in Galway, Ireland.