Medical Device QMS/Manufacturing Engineer — R&D to Production
Listed on 2026-10-06
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Engineering
Quality Engineering, Medical Device Industry, Biomedical Engineer, Manufacturing Engineer
Engineering Resource Group is seeking a Quality/Manufacturing Engineer to transfer medical device processes from R&D into production, ensuring QMS compliance and robust risk management. The role requires leading validations, PFMEA/DFMEA, CAPA and supplier oversight.
Responsibilities include IQ/OQ/PQ validations, supplier qualification and documentation such as DMR/DMR, with travel up to 10% and a potential for hybrid remote work. BS in Engineering and 5+ years in the field are expected.
We would love to welcome a new Medical Device QMS/Manufacturing Engineer — R&D to Production to our organisation in Princeton, NJ, United States.
We would love to welcome a new Medical Device QMS/Manufacturing Engineer — R&D to Production to our group in Princeton, NJ, United States.
For the Medical Device QMS/Manufacturing Engineer — R&D to Production position at Engineering Resource Group, we are reviewing applications now.
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