PA Consulting seeks an experienced Medical Device Quality Specialist Consultant to support development and lifecycle management of medical devices, including SaMD and combination products. You will ensure regulatory compliance, robust quality systems, and post‑market vigilance while collaborating with multi‑disciplinary teams.
Ideal candidates bring extensive experience with ISO 13485, IEC 62304, and ISO 14971, plus strong supplier quality and document control skills.
#J-18808-Ljbffr
Medical Device Quality & Regulatory Consultant in London employer: PA Consulting
At PA Consulting, we pride ourselves on being an excellent employer that fosters a collaborative and innovative work culture. As a Data Architect, you will have the opportunity to lead transformative projects in a hybrid working environment, allowing for flexibility while engaging with clients and colleagues. We are committed to your professional growth, offering continuous learning opportunities and the chance to work on cutting-edge AI-driven data solutions that make a real impact.