Product Development Engineer

JR United Kingdom; City of Edinburgh; On-site; GBP 50,000 - 70,000; Full time

Job summary

A leading MedTech company seeks an experienced engineer to lead post-design product development for invasive vascular and surgical care, ensuring patient safety and optimal product outcomes. The role involves overseeing the full product lifecycle and requires strong expertise in ISO 13485, usability engineering, and risk management.

Qualifications

• 5+ years in medical device R&D or development, focusing on post-design activities.
• Strong experience with ISO 13485 and full DHF responsibilities.
• Solid understanding of V&V processes and human factors.

Responsibilities

• Lead post-design development including usability and risk analysis.
• Drive design verification and validation, and manage transfer to manufacture.
• Define and maintain BoMs, materials, and support design for manufacture.

Skills

Usability Engineering

Risk Management

Design Verification

Validation Processes

Education

Engineering or Scientific Degree

Job description

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Cure Talent are delighted to be partnering with an innovative MedTech company dedicated to transforming patient safety, monitoring and outcomes in invasive vascular and surgical care.

We’re seeking an experienced engineer with deep working knowledge of ISO 13485 and proven capability across the post-design, full product lifecycle. You’ll be the technical lead, taking products from design through to successful manufacture and market release, managing all critical phases: Usability, Risk, V&V, Documentation, and Transfer to Manufacture.

Key Responsibilities Include:

• Leading post-design development across usability, human factors, and risk analysis incl. FMEA
• Driving design verification and validation, planning and executing V&V strategies
• Managing smooth transfer to manufacture and serving as liaison with CMOs
• Defining and maintaining BoMs, materials, and supporting design for manufacture principles

What We’re Looking For:

• 5+ years in medical device R&D or development, with ownership of post-design activities and an engineering or scientific degree
• Strong experience working under ISO 13485, with full DHF and regulatory documentation responsibility
• Skilled in usability engineering, human factors, and risk management e.g. FMEA
• Solid understanding of V&V processes and manufacturing transfer

If you’re eager to be at the forefront of medical device development and work with a company that prioritizes patient outcomes, we’d love to hear from you!