Quality Engineer with mandatory experience in the medical devices domain responsible for planning and executing validation activities aligned with ISO 13485 and ISO 14971, overseeing daily project operations at the client location, and supporting R&D new product development, design change management, product lifecycle management, risk management, and design verification & validation activities.
Roles & Responsibilities:
Plan and execute validation activities in alignment with ISO 13485 and ISO 14971.
Manage and oversee daily operations and projects at the client location as the primary link between client and project team.
Lead and support design verification and validation activities, including test method development and execution.