SIFo Medical provides hands-on support for MedTech companies in Quality & Supplier Management. What you'll get: A solid Quality Management System that is audit-proof ✅- We validate your Processes, Test Methods, Packaging- Handle your Product Development / Design Control & Risk ManagementSuppliers who comply with MDR & FDA requirements ✅- Supplier Selection (Sourcing MDR-compliant materials)- Supplier Audits- Supplier DevelopmentAfter working with SIFo… Show more SIFo Medical provides hands-on support for MedTech companies in Quality & Supplier Management. What you'll get: A solid Quality Management System that is audit-proof ✅- We validate your Processes, Test Methods, Packaging- Handle your Product Development / Design Control & Risk ManagementSuppliers who comply with MDR & FDA requirements ✅- Supplier Selection (Sourcing MDR-compliant materials)- Supplier Audits- Supplier DevelopmentAfter working with SIFo Medical you will have✅ a MDR-compliant Supply Chain✅ complete technical documentation✅ efficient manufacturing processes✅ significantly reduced complaint rates➡️ For more information, visit www.sifo-medical.com Show less

External Lecturer for:✅ Process Validation✅ Test Method Validation✅ Statistics in the Medical Device Industry➡️ For the latest training schedule, visit: https://www.tuvsud.com/de-de/store/akademie/seminare-technik/medizintechnik

Rethinking medicine.AVIMEDO is an online medical consultation service based in Austria. With AVIMEDO we provide a tool that makes it easy for patients to make a doctor's appointment quickly and without long waiting times. 🩺 Recognized specialists from Austria will be happy to advise you on your way to optimal health. 🚨 If you suffer from chronic or acute pain and want to quickly make a doctor's appointment via video call, go to:➡️ www.avimedo.com

Yes, I've been on the user side of medical devices too! This valuable experience lets me keep the big picture in mind in my daily work as a consultant.

In control of nonconforming product, complaint handling and CAPA; Carrying out root cause analysis; Driving effective corrective and preventive actions; Qualifying new suppliers; Performing internal and external audits etc.

In control of medical device development from design input to first customer delivery;Performing and coordinating relevant design phases; Transferring design into production; Designing production lines with state-of-the-art lean approaches; Performing PPAP (e.g. gage R&R, process characterization, validation and capability analysis, first article inspection etc.); Qualifying new suppliers; Performing internal and external audits etc.

Engineer responsible for the design of new sub-assemblies for semiconductor packaging machinery from concept phase, design, bill of materials, drawings