Senior Staff Mechanical Design Engineer

Location: Stryker R&D Instruments Innovation Centre, Cork

Hybrid Work

Division: Stryker IVS

News:

Plans Approved: €25.5m Stryker Innovation Centre Expansion | Carrigtwohill, Co. Cork. Stryker has received planning approval for a four-storey extension to its Innovation Centre in Carrigtwohill, marking another major step in its ongoing Irish expansion.

Who we want:
We’re looking for a Senior Staff Mechanical Engineer to join our dynamic team of innovators at our Innovation Centre in Cork. This hybrid role requires three days onsite, offering the perfect blend of collaboration and flexibility.

As a Senior Staff Design Engineer, you’ll partner across disciplines—Quality, Manufacturing, Regulatory, Clinical Sciences, Marketing, and Project Management—to drive success. You’ll have the chance to work on cutting-edge systems and play a pivotal role in designing and delivering next-generation interventional solutions that truly make a difference.

Learn more about our business here: Stryker IVS

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

Med Device 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

Minimum Qualifications (Required):

• Bachelor of Science in Engineering, Mechanical Engineering or BioMedical & 6+ years of 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

#IJ

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#materialanalysis

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#researchanddevelopment

Posted Date: 03/23/2026
This role will be posted for a minimum of 3 days.