Human-Machine Interaction Engineering specialist — regulatory strategy (mdr/fda) & bioprocess equipment
16 years delivering regulatory strategy (mdr/fda) and bioprocess equipment work for pharmaceuticals and manufacturing clients. I work to IEC 62304 and ASTM F2129, deliver in Creo and Minitab, 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.
Medical Device Engineering specialist — medical device design & verification & validation
Bioinformatics Engineering specialist — risk management iso 14971 & bioprocess equipment
Ergonomics Engineering specialist — bioprocess equipment & medical device design
Biological Engineering specialist — biocompatibility & bioprocess equipment
