Lubomír Šviantek Email
Global Regulatory Affairs Medical Device Project Manager @ Bausch Health Companies Inc.
Lubomír Šviantek's Location
Prague, Czechia
Lubomír Šviantek's Work
- Global Regulatory Affairs Medical Device Project Manager @ Bausch Health Companies Inc.
- Regulatory Affairs Medical Device Manager EMEA @ Bausch Health Companies Inc.
- Regulatory Affairs Medical Device Manager EMEA @ Valeant Pharmaceuticals
- Regulatory Affairs Medical Device Specialist EMEA @ Valeant Pharmaceuticals
- Technical Operation and Product Support Manager @ 贝克曼库尔特商贸(中国)有限公司
- Technical Operation and Technical Support Manager @ 贝克曼库尔特商贸(中国)有限公司
- Development Scientist @ 贝克曼库尔特商贸(中国)有限公司
Lubomír Šviantek's Education
- Charles University in Prague, Faculty of Science
Mgr. (Clinical and toxicological analysis)
2003 - 2008
Lubomír Šviantek's Skills
- Medical Device Directive
- Medical Device Product Development
- Management
- ISO 13485
- Product Knowledge
- 21 CFR Part 820
- Quality
- Medical Devices
- Ivdd
- Immunoassays
Lubomír Šviantek's Summary
Lubomír Šviantek, based in Prague, Czechia, is currently a Global Regulatory Affairs Medical Device Project Manager at Bausch Health Companies Inc., bringing experience from previous roles at Bausch Health Companies Inc., Valeant Pharmaceuticals and Immunotech Prague ltd (a Beckman Coulter company). Lubomír Šviantek holds a 2003 - 2008 Mgr. in Clinical and toxicological analysis @ Charles University in Prague, Faculty of Science. With a robust skill set that includes Medical Device Directive, Medical Device Product Development, Management, ISO 13485, Product Knowledge and more, Lubomír Šviantek contributes valuable insights to the industry. Lubomír Šviantek has 1 email on RocketReach.
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