Senior Mechanical Engineer

Stryker Group; Cork; Hybrid; EUR 50,000 - 70,000; Full time

Job summary

A leading medical technology company is looking for a Senior Engineer to join its Neurosurgical team in Cork. This hybrid role offers a unique opportunity to work on innovative medical devices impacting patient care. The ideal candidate will have a Bachelor's degree in Engineering, at least 2 years of relevant experience, and strong mechanical engineering skills.

Qualifications

• Bachelor's degree in Engineering or related field.
• 2+ years of work experience.
• Strong understanding of mechanical engineering practices.

Responsibilities

• Research, design, and develop medical device components.
• Collaborate with various teams to ensure project success.
• Create and refine engineering documentation for compliance.

Skills

Mechanical Engineering

Biomedical Engineering

GD&T Knowledge

CAE Tools

Education

Bachelor of Science in Engineering

Job description

Permanent hybrid role based in the Innovation Centre, Carrigtwohill, Cork

Who we want:
We are seeking a passionate and driven Senior Engineer to join our Neurosurgical team. This is a unique opportunity to work at the intersection of advanced medical technology and work on patient impacting technology.

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