Mark Steckel

Vice President Regulatory at MedAlliance Swiss Medical Technology

Mark has more than 30 years of medical device experience, holding senior roles in Product Development, Regulatory and Clinical Research. He has in-depth experience bringing complex and novel Class III devices from concept through to commercialization including absorbable polymer implants and device-drug combination products. He was most recently VP R&D Clinical Regulatory for Terumo in Europe. Some of his previous positions include Senior Research Fellow in Drug Delivery at Boston Scientific, Director R&D at Biotronik, Chief Technology Officer at Capella, and Director R&D at JNJ Mitek.

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Previous companies

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Timeline

  • Vice President Regulatory

    Current role

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