Jon Lang has extensive experience in medical device development and regulatory affairs. They began their career in 1997 as a Manufacturing Quality Control and Mixing Specialist at Chiron/Bayer Diagnostics, where they supported formulation and filling departments. Over the years, Jon held various roles including Manufacturing Engineering Supervisor and Regulatory Affairs Manager at Bionostics and Fresenius Medical Care North America, respectively. Currently, they serve as the Director of Regulatory Affairs for Patient Interface & Software at Philips. Jon is also pursuing a Medical Device Certificate in Regulatory Affairs at Worcester Polytechnic Institute.
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