Corina Nicolae
Mechanical Project Manager @Xds Oxford
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WORK HISTORY
Mechanical Project Manager @Xds Oxford
Oxford, GB
I manage the design and delivery of bespoke beamline components for advanced research facilities. I lead projects from concept through to manufacture, combining mechanical design expertise with project management to ensure reliable, high-performance systems.
EDUCATION
Nicolae Balcescu National College
Mathematics and Computer Science
University of Southampton
MEng Mechanical Engineering / Biomedical Engineering, Mechanical Engineering
ABOUT CORINA NICOLAE
PRINCE2-certified Technical Project Manager and Mechanical Engineer with extensive experience developing complex electromechanical systems within the medical devices industry and ensuring compliance with key standards such as ISO 60601 and ISO 14971. I have contributed to large-scale New Product Introduction (NPI) programmes in medical robotics and bring hands-on expertise across a wide range of areas including product development, regulatory compliance, CE marking, design integration, design verification and validation, hardware and software integration, and system troubleshooting.I thrive in highly regulated environments, consistently delivering technically complex projects on time, within budget, and in full compliance with applicable standards. My experience allows me to bridge the gap between detailed engineering execution and structured programme delivery, supporting the development of innovative medical technologies from concept through to manufacturing readiness. Product Development & Systems Integration – Experience delivering complex electromechanical systems, coordinating multidisciplinary teams to ensure seamless integration of hardware, firmware, and software. Project & Agile Management – PRINCE2-certified Technical Project Manager experienced in Agile methodologies, sprint planning, and backlog management using JIRA. Currently preparing for PMP® certification. Regulatory & Compliance – Strong background working within regulated medical device environments, including CE marking, ISO 60601, ISO 14971, and MDR. Risk Management & Product Development – Experienced in driving structured risk management processes that ensure product safety, reliability, and regulatory compliance throughout the product lifecycle. Cross-Functional Programme Delivery – Experienced in coordinating engineering, quality, regulatory, and manufacturing teams to deliver complex medical device projects and support successful product development and introduction.
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