Senior Staff Design Engineer, R&D
Stryker
Cork, Ireland
This role is true R&D where you as a Snr Staff Engineer will be part of a group that has complete design control for all extremities power tools. In Cork, the team own the strategy and the portfolio. The team meet with the surgeons and gain a lot of clinical exposure. You will work with a multi disciplinary team including software, electrical and mechanical.
Who we want:
Designs and develops mechanical component assemblies or subassemblies for mechanical and/or electromechanical medical devices.
What you will do:
Technical Responsibilities:
- Lead research, design, development, modification and evaluation of modules, assemblies, or subsystems;
- Apply and mentor others on advanced engineering theories, principles, and concepts;
- Translate user needs to design inputs/ specifications and produce complex system level designs independently;
- Conduct, design, and select advanced prototyping and testing;
- Lead and guide in correction of complex product design issues;
- Conduct technology exploration and influence application in the business;
- Develop invention disclosures, patents or trade secrets.
Business Responsibilities:
- Contribute to competitive and market strategy by demonstrating in-depth knowledge of the market, customer dynamics and competitive offerings;
- Apply strong understanding of clinical procedures to enhance product development;
- Contribute and execute customer facing activities like voice of customer and customer centric design in partnership with internal and external stakeholders;
- Demonstrate financial acumen.
Compliance:
- Mentor others as a business unit expert on the usage of industry standards, including design requirements and test strategies per applicable regulations;
- Lead others to create and refine engineering documentation, such as the Design History file and create more progressive technical content;
- Contribute to R&D procedures and development of industry standards working closely with cross-functional business units.
General Responsibilities:
- Work cooperatively with R&D, Quality, Manufacturing, Regulatory, Clinical, Marketing and Project Management to ensure project success;
- Identify and lead the creation of or improvements to procedures, policies, processes, systems, and technology required;
- Develop, Research, Prototype, leveraging multiple methodologies for evaluation;
- Contribute to complex product development through release and lead one technical area of expertise;
- Hold self and others accountable to deliver high quality results with passion, energy and drive to meet business priorities;
- Mentor, develop and inspire others in current and future roles;
- Collaborate and influence others on cross functional teams advancing partnerships to achieve business objectives.
Required Qualifications:
- Bachelor of Science in Engineering, Mechanical Engineering or BioMedical & 6+ years of mechanical design work experience.
Preferred Qualifications (Strongly desired):
Technical Skills:
- Experience in developing and optimizing complex designs for mechanical/electro-mechanical assemblies incorporating DFM principles;
- Experience in creating engineering drawings, models, applying GD&T and CAE tools to optimize the design;
- In-depth knowledge of materials, manufacturing and processing methods and technologies to support complex product development;
- Ability to communicate complex plans and technical information to team members.
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