Staff Mechanical Design Engineer, R&D
Staff Mechanical Design Engineer, R&D
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Job Description
Staff Mechanical Design Engineer R&D
Permanent Hybrid role based in the Innovation Centre Carrigtwohill
Role Summary:
Join our innovative team as a Mechanical Design Engineer (R&D) to spearhead the development of a ground-breaking medical device aimed at tackling blood loss during medical procedures. This role offers the unique opportunity to collaborate with electronic and software engineers to design and develop a commercial product that will elevate the standard of care for some of the most vulnerable patients. Engage directly with caregivers gather user feedback on prototypes and support clinical studies to refine your designs and contribute to safer surgical outcomes. Be a part of a mission-driven project that promises to make a significant impact on healthcare.
Who we want:
As a Staff Mechanical Design Engineer R&D you will perform a wide variety of technical work in planning design and implementation of mechanical design for medical devices used by surgeons and healthcare surgical staff to allow them to plan and perform their procedures. This role will be a key contributor to the mechanical design of embedded medical devices supporting our quantification of blood loss research.
What you will do:
Technical Responsibilities:
Under minimal supervision research design develop modify and verify components/modules for medical devices
Translate design inputs to engineering specifications and produce sub-system level designs
Develop and analyze solutions prototyping one or more options to provide proof of concept
Apply fundamental and some advanced concepts practices and procedures for problem solving
Business Responsibilities:
Demonstrate advanced understanding of customer needs and design inputs
Demonstrate proficiency with products intended use and clinical procedures
Learn how the financial models are constructed
Med Device Compliance:
Follow fundamental industry standards design requirements and test strategies which apply to regulatory requirements
Independently create or refine engineering documentation such as the Design History file
Follow R&D procedure like design controls and risk management per the Quality Management System
General Responsibilities:
Under minimal supervision work with R&D Quality Manufacturing Regulatory Clinical Marketing and Project Management to ensure project success
Quickly process and assimilate procedures policies processes systems and technology required
Work on complex problems applying advanced experience and learnings
Demonstrate ownership and prioritize work with minimal supervision
Works as key member of the team collaborating with others and solidifying relationships
Minimum Qualifications (Required):
Bachelor of Science in Engineering Mechanical Engineering or BioMedical & 4 years of work experience
Preferred Qualifications (Strongly desired):
Technical Skills:
Working knowledge and understanding of mechanical engineering practices and design principles
Technical ability to create engineering drawings and models applying GD&T and CAE tools
Demonstrated ability to apply knowledge of materials and manufacturing processes to product design
Ability to Communicate basic plans and technical information to team members
Required Experience:
Staff IC
Employment Type
Full-Time
