Reto Pusterla Email & Phone Number
Head Regulatory Affairs @ BioHorizons Camlog Group Global
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Reto Pusterla Location
- Basel, BS, CH
Reto Pusterla Work
- 2014 -now Head Regulatory Affairs @
- 2014 -2014 Senior Project Manager Quality EMEA @
- 2013 -2013 Head Complaint Handling Unit International @
- 2006 -2013 Group Manager RA and Clinical Affairs Spine @
- 2006 -2013 Group Manager RA and CA Spine @
Reto Pusterla Education
- University of Applied Sciences and Arts Northwestern Switzerland FHNW
CAS (CARAQA)
2021-2021 - Biozentrum, University of Basel
Master of Science - MS (Cell/Cellular and Molecular Biology)
1993-1998
Reto Pusterla Skills
- Leadership
- Design Control
- Spine
- Surgical Instruments
- ISO 14971
- Biomaterials
- Complaint Management
- Biomedical Engineering
- Regulatory Affairs
- Process Improvement
- Medical Devices
- Quality Assurance
- Strategic Planning
- Compliance
- Quality System
- V&V
- Capital Equipment
- Regulatory Compliance
- Orthopedic
- Neurosurgery
- Regulatory Submissions
- Remediation
- Product Launch
- CAPA
- FDA
- Orthopedics
- Market Development
- ISO 13485
Reto Pusterla Summary
- Reto Pusterla, based in Basel, BS, CH, is currently a Head Regulatory Affairs at CAMLOG Biotechnologies AG. Reto Pusterla brings experience from previous roles at DePuy Synthes, Synthes GmbH and Synthes Spine. Reto Pusterla holds a 2021 - 2021 CAS in CARAQA @ University of Applied Sciences and Arts Northwestern Switzerland FHNW. With a robust skill set that includes Leadership, Design Control, Spine, Surgical Instruments, ISO 14971 and more.
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