Mark Steckel Email & Phone Number
VP Global Regulatory Affiars @ MedAlliance Swiss Medical Technology
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Mark Steckel Location
- Glasgow, GB
Mark Steckel Work
- now
- 2020 - now VP Global Regulatory Affiars @
- 2018 - 2020 VP R and D RA QA @
- 2012 - 2018 Vice President of R and D, Clinical Affairs and Regulatory Affairs @ Vascutek Ltd, a TERUMO Company
- 2010 - 2012 R and D Director @
- 2008 - 2010 Director of DREAMS (Drug Eluting Absorbable Metal Stent) Development @
- 2005 - 2008 Chief Technology Officer, VP R and D, Clinical and Regulatory @
- 2001 - 2006 Senior Research Fellow @
- 1988 - 2001 Director R and D @
Mark Steckel Education
- Massachusetts Institute of Technology
Master’s Degree (Materials Science and Engineering)
1984 - 1987 - Drexel University
Mark Steckel Skills
- Medical Devices
- Biomedical Engineering
- Design Control
- R&D
- FDA
- Biomaterials
- Drug Delivery
- Biotechnology
- Catheters
- Validation
- Clinical Trials
- Materials Science
- Clinical Research
- Interventional Cardiology
- ISO 13485
- Commercialization
- Start-ups
- Stents
- Regulatory Submissions
- Market Development
- ISO 14971
- V&V
- Product Development
- Cross-functional Team Leadership
- Product Launch
- Life Sciences
- Clinical Development
- Quality System
- Cross Functional Team Leadership
- Science
- Business Strategy
- Strategy
- Marketing
- Start Ups
Mark Steckel Summary
- Mark Steckel, based in Glasgow, GB, is currently a VP Global Regulatory Affiars at MedAlliance Swiss Medical Technology. Mark Steckel brings experience from previous roles at Lumenology Ltd, MedAlliance Swiss Medical Technology, Vascutek Ltd, a TERUMO Company and Biosensors International Group, Ltd. Mark Steckel holds a 1984 - 1987 Master’s Degree in Materials Science and Engineering @ Massachusetts Institute of Technology. With a robust skill set that includes Medical Devices, Biomedical Engineering, Design Control, R&D, FDA and more. Mark Steckel has 3 emails on RocketReach.
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