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(Junior) Expert Biocompatibility(m/w/x)
Evaluating biocompatibility of medical devices and raw materials for kidney disease treatment at a medical product developer. Knowledge of ISO 10993, FDA CFR 820, and ISO 13485 for medical devices required. Standard work week.
Anforderungen
- Bachelor’s or master’s degree in scientific, engineering, or similar technical field
- 1 to 5 years of related working experience
- First experience in writing biocompatibility evaluations
- Knowledge of biocompatibility testing and evaluations of medical devices according to ISO 10993
- Application of Design Control and Risk Management, knowledge of FDA CFR 820, ISO 13485, and ISO 14971
- Knowledge of medical device risk management process and related regulations
- Experience with product or design and development or quality engineering of sterile disposables
- Ability to communicate technical information to non-technical audiences
- Familiarity with agile methodology
- First experience with ALM and PDM systems
- Familiarity with durables and disposables of medical devices
- Fluency in German and English, both written and spoken
- Willingness to travel on an average monthly cadence and to work in different time zones
Aufgaben
- Evaluate biocompatibility of medical devices
- Support safety and risk assessments based on raw materials
- Interpret and evaluate analytical and biological tests
- Assist in compiling biological safety assessments
- Derive biocompatibility strategy details
- Act as sponsor and monitor for biocompatibility studies
- Coordinate biocompatibility project support
- Align sampling and testing strategies
- Coordinate global laboratory partner alignment
- Manage biocompatibility files for assigned product groups
- Contribute to supplier agreements for biocompatibility
- Monitor regulation changes and ensure timely implementation
Berufserfahrung
- 1 - 5 Jahre
Ausbildung
- Bachelor-AbschlussODER
- Master-Abschluss
Sprachen
- Deutsch – verhandlungssicher
- Englisch – verhandlungssicher
Tools & Technologien
- ISO 10993
- FDA CFR 820
- ISO 13485
- ISO 14971
Benefits
Karriere- und Weiterentwicklung
- Individual career planning
Weiterbildungsangebote
- Professional development opportunities
Startup-Atmosphäre
- Innovative thinking culture
Lockere Unternehmenskultur
- Collegial culture
Noch nicht perfekt?
- Fresenius Medical Care D. GmbHVollzeitnur vor OrtBerufserfahrenSankt Wendel
- Fresenius Medical Care D. GmbH
Projektmanager - Qualitätssysteme(m/w/x)
Vollzeitnur vor OrtBerufserfahrenSankt Wendel - HYDAC
Mitarbeiter Tax Compliance(m/w/x)
Vollzeitnur vor OrtJuniorNeunkirchen - Fresenius Medical Care D. GmbH
Pharmaziepraktikum(m/w/x)
VollzeitPraktikumnur vor OrtSankt Wendel - Fresenius Medical Care
Apotheker im praktischen Jahr(m/w/x)
VollzeitPraktikumnur vor OrtSankt Wendel
(Junior) Expert Biocompatibility(m/w/x)
Evaluating biocompatibility of medical devices and raw materials for kidney disease treatment at a medical product developer. Knowledge of ISO 10993, FDA CFR 820, and ISO 13485 for medical devices required. Standard work week.
Anforderungen
- Bachelor’s or master’s degree in scientific, engineering, or similar technical field
- 1 to 5 years of related working experience
- First experience in writing biocompatibility evaluations
- Knowledge of biocompatibility testing and evaluations of medical devices according to ISO 10993
- Application of Design Control and Risk Management, knowledge of FDA CFR 820, ISO 13485, and ISO 14971
- Knowledge of medical device risk management process and related regulations
- Experience with product or design and development or quality engineering of sterile disposables
- Ability to communicate technical information to non-technical audiences
- Familiarity with agile methodology
- First experience with ALM and PDM systems
- Familiarity with durables and disposables of medical devices
- Fluency in German and English, both written and spoken
- Willingness to travel on an average monthly cadence and to work in different time zones
Aufgaben
- Evaluate biocompatibility of medical devices
- Support safety and risk assessments based on raw materials
- Interpret and evaluate analytical and biological tests
- Assist in compiling biological safety assessments
- Derive biocompatibility strategy details
- Act as sponsor and monitor for biocompatibility studies
- Coordinate biocompatibility project support
- Align sampling and testing strategies
- Coordinate global laboratory partner alignment
- Manage biocompatibility files for assigned product groups
- Contribute to supplier agreements for biocompatibility
- Monitor regulation changes and ensure timely implementation
Berufserfahrung
- 1 - 5 Jahre
Ausbildung
- Bachelor-AbschlussODER
- Master-Abschluss
Sprachen
- Deutsch – verhandlungssicher
- Englisch – verhandlungssicher
Tools & Technologien
- ISO 10993
- FDA CFR 820
- ISO 13485
- ISO 14971
Benefits
Karriere- und Weiterentwicklung
- Individual career planning
Weiterbildungsangebote
- Professional development opportunities
Startup-Atmosphäre
- Innovative thinking culture
Lockere Unternehmenskultur
- Collegial culture
Über das Unternehmen
Fresenius Medical Care D. GmbH
Branche
Healthcare
Beschreibung
The company is dedicated to improving the lives of patients with chronic kidney disease through innovative, high-quality products and treatments.
Noch nicht perfekt?
- Fresenius Medical Care D. GmbH
(Senior) Expert Biocompatibility(m/w/x)
Vollzeitnur vor OrtBerufserfahrenSankt Wendel - Fresenius Medical Care D. GmbH
Projektmanager - Qualitätssysteme(m/w/x)
Vollzeitnur vor OrtBerufserfahrenSankt Wendel - HYDAC
Mitarbeiter Tax Compliance(m/w/x)
Vollzeitnur vor OrtJuniorNeunkirchen - Fresenius Medical Care D. GmbH
Pharmaziepraktikum(m/w/x)
VollzeitPraktikumnur vor OrtSankt Wendel - Fresenius Medical Care
Apotheker im praktischen Jahr(m/w/x)
VollzeitPraktikumnur vor OrtSankt Wendel