Gisbert Ranzinger
About Gisbert Ranzinger
Gisbert Ranzinger is the Director of Regulatory Affairs and Quality Assurance at Teleflex Medical's Kernen facilities, with over 18 years of experience in the company and extensive expertise in the medical device industry.
Current Position at Teleflex Medical
Gisbert Ranzinger serves as the Director of Regulatory Affairs and Quality Assurance (RA/QA) at Teleflex Medical, overseeing the Kernen facilities. In this role, he is responsible for ensuring compliance with regulatory standards and maintaining high levels of quality assurance within the organization. His extensive experience in RA/QA makes him a key figure in the company's operations.
Previous Roles at Teleflex
Before becoming the Director QU/RA at the Kernen facilities, Gisbert Ranzinger held the position of Director RA/QA at Teleflex. Over his 18-year tenure with the company, he has contributed significantly to the regulatory and quality assurance frameworks within the medical device sector. His long-standing association with Teleflex highlights his expertise and dedication to the field.
Educational Background
Gisbert Ranzinger studied at Ludwig-Maximilians Universität München, also known as the University of Munich, where he completed a Staatsexamen und Facharzt HNO and achieved a degree in Human Medizin. His studies spanned seven years, from 1971 to 1978. This extensive educational background has provided him with a strong foundation in medical science and regulation.
Experience in Regulatory Affairs and Quality Assurance
With over 18 years of experience at Teleflex Medical, Gisbert Ranzinger has amassed extensive expertise in regulatory affairs and quality assurance, especially within the medical device industry. His work ensures that the company's products meet stringent regulatory standards and maintain high-quality levels, contributing to the reliability and safety of Teleflex's offerings.
Contributions to European Operations
Based in Stuttgart, Germany, Gisbert Ranzinger plays a pivotal role in supporting Teleflex Medical's European operations. His regulatory affairs and quality assurance expertise are integral to maintaining compliance with European medical device regulations, thereby supporting the company's strategic initiatives and operational goals in Europe.