Senior Design Engineer R&D
Senior Design Engineer R&D
Stryker
Cork, Ireland
We are currently seeking a Senior Design Engineer located at our Global R&D Innovation Centre in Cork, Ireland, to work on the next generation of surgical devices.
What you will do:
As a Senior Design Engineer, you will work on the mechanical design for devices used by surgeons and surgical staff to allow them to plan and perform their procedures, and work in a multi-disciplinary group to deliver these devices from concept, through design and manufacturing development and launch them to market. You will design, develop, refine and evaluate mechanical components, assemblies or subsystems for mechanical and/or electro-mechanical medical devices and implants. You will execute product development projects, and work on technical aspects of product commercialization.
Who we want:
- Dedicated Achievers. Relentless about quality, people who thrive in a fast-paced environment and will stop at nothing to ensure a project is complete and meets regulations and expectations
- Motivated product launchers. Engineers who bring strategic direction and drive for execution to ensure products are developed and launched with precision
- Goal-oriented developers. Keeping the customer and requirements squarely in focus, people who deliver safe and robust solutions.
- User-focused creators. People who imagine with the user in mind, developing technology that helps change patients’ lives.
- Curious learners. People who seek out cutting-edge research and information to expand and enhance their ability to develop new ideas into reality.
Key Areas of Responsibility: 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.
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.
Preferred Qualifications: What you will need (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.
Preferred Skills/Engineering tools:
- Experience with ProEngineer or similar software is preferred.
Minimum Qualifications: What you will need (must have):
Education Requirements:
- Bachelor of Science in Engineering, Mechanical Engineering, BioMedical or Masters in related discipline & 2+ years of work experience.
