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3 Days Left Senior Mechanical Design Engineer
1 month ago
Location: Stryker R&D Instruments Innovation Centre in Cork
In this role as a Senior Mechanical Design Engineer, you will be part of a team working on the next generation of technologies needed to advance our Ear, Nose and Throat (ENT) product portfolio. You will be responsible for designing and developing these devices and working with colleagues to integrate these into the overall device architecture and the ecosystem of complementary devices.
You will be also responsible for the creation of system requirements/architecture specifications for new products. It is expected that you will become highly familiar with ENT surgical procedures as part of your role.
This role will work closely with technical, and business leads from multiple areas to progress fundamental research and product design concepts for ENT applications. This role will have the opportunity to partner closely with a global R&D team, multidisciplined clinical teams and marketing as we collectively advance ear, nose & throat and neurosurgery to transform the lives of patients.
Who we want:
This is an individual contributor role that requires the use of judgement in applying professional expertise and is expected to work independently with minimal supervision. This job requires practical experience and an understanding and application of procedures and concepts of own discipline. The job requires attention to detail in making evaluative judgements based on the analysis of factual information.
This role will suit:
- Curious learners. Engineers who seek out cutting-edge research and information to expand and enhance their ability to develop software.
- Collaborative partners. People who build and leverage cross-functional relationships to bring together ideas, information, use cases, and industry analyses to develop best practices.
- Solutions-oriented enthusiast. People who can come up with creative designs to solve complex engineering challenges.
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 product's intended use and clinical procedures
• Learn how the financial models are constructed
• 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 & a minimum 2 years of relevant work experience
Preferred Experience and Skills (Strongly desired):
Technical Skills:
• Working knowledge and understanding of mechanical engineering practices and design principles
• Proficient in 3D CAD (Solidworks, CREO or equivalent), 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
• Experience of the Medical Device Industry or other highly regulated industry
• Willingness to travel internationally for live surgery visits and global partner collaboration
• Self-starter with demonstrated efficient work methods, analytical & problem solving skills and ability to handle multiple tasks using independent judgement in a fast paced environment.
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