Job Description

Work Flexibility: Hybrid

Senior Mechanical Design Engineer

Location: Stryker R&D Instruments Innovation Centre, Cork

Hybrid Working

News:

Plans Approved: €25.5m Stryker Innovation Centre Expansion | Carrigtwohill, Co. Cork. Big moves in Cork’s life sciences cluster — 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 Design 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 Design Engineer, you’ll partner across disciplines—Quality, Manufacturing, Regulatory, Clinical Sciences, Marketing, and Project Management—to drive success. Under minimal supervision, 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:

• 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

Minimum Qualifications (Required):

• Bachelor of Science in Engineering, Mechanical Engineering or BioMedical & 2+ 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

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Travel Percentage: 10%