Design Quality Engineer: Medical Devices & Risk Management
Listed on 2026-10-18
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Engineering
Quality Engineering, Biomedical Engineer, Medical Device Industry
Actalent is seeking a Design Quality Engineer to lead ISO-based risk management for medical devices across the lifecycle. The role collaborates with R&D, Regulatory Affairs, Manufacturing, and Quality Systems to ensure design controls align with QSR/21 CFR 820.30 and to maintain robust risk documentation.
Based in Fremont, CA, this contract position offers exposure to hazard analysis, FMEA, and post-market surveillance, with opportunities to mentor teams and drive continuous improvement in risk
This is an excellent role to take on the Design Quality Engineer:
Medical Devices & Risk Management role at Actalent.
Full responsibilities and requirements are described in the listing above.
Learn more about the Design Quality Engineer:
Medical Devices & Risk Management role in the description above.
We appreciate your interest in this position.
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