Design Quality Assurance Engineer

Updated: June 16, 2024 08:33 PM GMT

Sandoz UK & Ireland

Cambridge

Job Description

Your Key Responsibilities:

Your Responsibilities Include, But Not Limited To
• Prepare medical device and drug/device combination product design and development documentation and compilation of Design History Files and/or Technical Files in collaboration with multi-disciplinary project teams.
• Interface with Quality Assurance functions to ensure compliance with company QMS and international standards and regulations.
• Guide and/or support project teams through design assurance and compliance activities and ensure best practices.
• Participate in and/or lead design reviews.
• Reporting of technical complaints / adverse events / special case scenarios related to Sandoz products within 24 hours of receipt.

Essential Requirements

What you’ll bring to the role:
• Masters, PhD, or university degree in the field of engineering, Quality, life sciences, or other relevant subject
• Good working knowledge of medical device and drug-device combination product development... More Detail