Bioprocess Engineering specialist — medical device design & regulatory strategy (mdr/fda)
9 years delivering medical device design and regulatory strategy (mdr/fda) work for medical devices and manufacturing clients. I work to IEC 60601-1 and ISO 10993, deliver in COMSOL and 3-matic, and hand over a complete, checked document set with a clear design basis so your reviewer or authority can follow every assumption.
Matched on discipline, software overlap and industry experience.
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