CREGG are now recruiting for a R&D Engineer II.
This is a fantastic opportunity to join a world leading Medical Device company in Co.
Galway working as an R&D Engineer, on the latest products and technologies with great career progression opportunities.
Job Purpose
Responsible for supporting commercialization of next-generation minimally invasive medical devices for the treatment of valvular heart disease.
The successful candidate will work as a member of a team within a dynamic New Product Development organization specialized in transcatheter heart valve system development.
Under limited supervision/guidance, compiles, analyzes, and reports operational, test, and research data to enable design intent to be maintained on commercialized products whilst also helping provide post-launch support by being a source of key product and clinical knowledge.
Key Responsibilities
Use of design change process to ensure proposed changes are systematically and thoroughly analyzed before beginning the change process.
Works cross-functionally with project management, quality, manufacturing, regulatory, clinical, and marketing to ensure project success.
Work collaboratively with manufacturing to reduce product costs through design improvements.
Works with other functions to understand feedback from the market, providing design knowledge input to understand device performance and anatomy interaction, look for opportunities for device improvement, and interact with physicians as necessary to optimize outcomes.
Interfaces with vendors and physicians where projects require.
Demonstrates design control knowledge through generation of high-quality deliverables.
Maintain product performance through Quality Investigations and ensuring rigorous support for design changes.
Works independently to plan and schedule own activities necessary to meet timelines.
Designs and coordinates standard engineering tests and experiments.
Designs, procures, and fabricates tooling and fixtures.
Performs troubleshooting on products/process problems as related to design, material, or process.
Summarizes, analyzes, and draws conclusions from test results.
Prepares standard reports/documentation to communicate results to the technical community.
Responsible for engineering documentation.
Invents/creates concepts and designs for new products/processes and submits idea disclosures.
May train and/or provide work direction to technicians and interns.
Maintains a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures.
Qualifications
HETAC Level 8 Degree in a relevant Technical Discipline, preferably Mechanical, Polymer, Materials, or Biomedical Engineering.
R&D/technical experience, preferably in the healthcare industry.
Excellent interpersonal and communication skills with proven leadership abilities.
Excellent analytical and problem-solving skills.
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