Regulatory Affairs Medical Devices Jobs in Bayern
1 - 15 von 29
Suchergebnisse - Regulatory Affairs Medical Devices Jobs in Bayern
PAUL HARTMANN AG-Heidenheim
Ideally initial professional experience in the medical device environment or another regulatory field is a plus
• Knowledge and/or experience in the areas of medical devices, technical documentation and regulatory product documentation, conformity...
FotoFinder Systems GmbH-Bad Birnbach
Qualitätssicherung und Regulatory Affairs
• Erstellung, Pflege und Weiterentwicklung der Risikoanalysen (FMEA, Fault Tree Analysis)
• Sicherstellung der Einhaltung regulatorischer Anforderungen (MDR, ISO 13485) im Risikomanagementprozess
• Entwicklung...
stepstone.de -
PAUL HARTMANN AG-Heidenheim
Ideally initial professional experience in the medical device environment or another regulatory field is a plus
• Knowledge and/or experience in the areas of medical devices, technical documentation and regulatory product documentation, conformity...
MED-EL-Garmisch-Partenkirchen
discipline, with a health science or biomedical component e.g. HTA, public health, clinical research, regulatory affairs
• At least 2 years medical device or regulatory affairs work experience is strongly preferred, graduates with any biomedical related...
jobninja.com -
PAUL HARTMANN AG-Heidenheim
Ideally initial professional experience in the medical device environment or another regulatory field is a plus
• Knowledge and/or experience in the areas of medical devices, technical documentation and regulatory product documentation, conformity...
MED-EL-Rosenheim
discipline, with a health science or biomedical component e.g. HTA, public health, clinical research, regulatory affairs
• At least 2 years medical device or regulatory affairs work experience is strongly preferred, graduates with any biomedical related...
jobninja.com -
FSQ Functional Safety & Quality Experts GmbH-München
FSQ Experts make innovative technology safer!
FSQ Experts GmbH offers medical technology companies precise and pragmatic solutions to overcome know-how or resource bottlenecks in the areas of quality management, regulatory affairs or system...
join.com -
MED-EL-München
discipline, with a health science or biomedical component e.g. HTA, public health, clinical research, regulatory affairs
• At least 2 years medical device or regulatory affairs work experience is strongly preferred, graduates with any biomedical related...
jobninja.com -
PAUL HARTMANN AG-Heidenheim
Collaboration with other departments e. g. marketing, production, supply chain, regulatory affairs
• Supporting the wider company in the maintenance and updating of documentation in accordance with relevant requirements
• Ensuring product compliance to all...
mindmatch.ai -
ZEISS-München
and cross-location project team for software systems running on medical devices or medical software-only products, as advisor and supporter of the project manager and the project team
• Analyze and review the product documentation, as well as approve...
stepstone.de -
MED-EL-Kempten (Allgäu)
component e.g. HTA, public health, clinical research, regulatory affairs
• At least 2 years medical device or regulatory affairs work experience is strongly preferred, graduates with any biomedical related experience e.g. in pharmaceutical industries...
mindmatch.ai -
PAUL HARTMANN AG-Heidenheim
Ideally initial professional experience in the medical device environment or another regulatory field is a plus
• Knowledge and/or experience in the areas of medical devices, technical documentation and regulatory product documentation, conformity...
MED-EL-Kempten (Allgäu)
About MED-EL
MED-EL is a leading manufacturer of innovative medical devices for the treatment of various types and degrees of hearing loss. Our unique portfolio of implantable hearing solutions benefits thousands of individuals in more than 140...
mindmatch.ai -
PAUL HARTMANN AG-Heidenheim
Ideally initial professional experience in the medical device environment or another regulatory field is a plus
• Knowledge and/or experience in the areas of medical devices, technical documentation and regulatory product documentation, conformity...
MED-EL-Kempten
discipline, with a health science or biomedical component e.g. HTA, public health, clinical research, regulatory affairs
• At least 2 years medical device or regulatory affairs work experience is strongly preferred, graduates with any biomedical related...
jobninja.com -
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