Company Pension

Health Insurance

Education Reimbursement

Corporate Events

Personal Development

• Leads the design and development of complex medical devices from concept through to design freeze
• Solves high-level engineering challenges using advanced materials knowledge, precision manufacturing methods, and data-driven decision making
• Acts as a subject matter expert in catheter systems, extrusion-based assemblies, and biomaterials, influencing design direction and technical standards
• Develops and executes verification and validation protocols (IQ/OQ/PQ), ensuring compliance with ISO 13485 and FDA 21 CFR Part 820
• Manages cross-functional technical projects, balancing design intent, manufacturability, and regulatory requirements
• Leads FMEA, risk analysis, and root cause investigations to ensure robust design and process outcomes
• Provides technical mentoring and reviews for junior engineers and project teams, helping to build capability and ensure knowledge transfer
• Drives innovation by exploring emerging technologies, novel components, and automation opportunities
• Develops and maintains detailed documentation including DHFs, BOMs, drawings, and test reports in compliance with QMS requirements
• Engages directly with customers to understand application needs, presenting technical solutions and leading design iterations

• Third-level qualification in Engineering or Science, preferably Mechanical or Biomedical; minimum Bachelor’s degree in Science, Technology, Engineering, or a related discipline (Mechanical, Manufacturing, Automation, or equivalent).
• Proven design capability with CAD systems, ideally Solid Edge.
• Senior-level candidates should have a minimum of 4 years’ relevant experience.
• Excellent interpersonal and communication skills, with the ability to collaborate effectively across teams