Regulatory Affairs Medical Devices Jobs in Baden-Württemberg
1 - 15 von 20
Suchergebnisse - Regulatory Affairs Medical Devices Jobs in Baden-Württemberg
Neuroloop GmbH-Freiburg im Breisgau
a comparable qualification
• You have several years of relevant professional experience in the field of medical device regulation
• You have extensive knowledge of regulatory affairs with a focus on international product approvals
• You have in-depth...
stepstone.de -
PAUL HARTMANN AG-Herbrechtingen
Affairs role within an international company
• Qualification as PRRC according to MDR
• Comprehensive knowledge of the regulatory requirements of medical device (e.g. MDR, MDD, MPG/MPDG/MPSV, MEDDEV, EN ISO 13485, 21 CFR 820), as well as personal...
IVF Hartmann Holding AG-Heidenheim an der Brenz
in a Regulatory Affairs role within an international company.
• Qualification as PRRC according to MDR.
• Comprehensive knowledge of the regulatory requirements of medical devices (e.g., MDR, MDD, MPG/MPDG/MPSV, MEDDEV, EN ISO 13485, 21 CFR 820), as...
appcast.io -
PAUL HARTMANN AG-Herbrechtingen
Affairs role within an international company
• Qualification as PRRC according to MDR
• Comprehensive knowledge of the regulatory requirements of medical device (e.g. MDR, MDD, MPG/MPDG/MPSV, MEDDEV, EN ISO 13485, 21 CFR 820), as well as personal...
JOTEC GmbH-Hechingen
Competency to effectively manage and motivate teams to achieve corporate, departmental and program goals on time Efficiency in managing and motivating direct reports to maximize writers' contributions and career development Familiarity with medical devices...
PAUL HARTMANN AG-Herbrechtingen
Affairs role within an international company
• Qualification as PRRC according to MDR
• Comprehensive knowledge of the regulatory requirements of medical device (e.g. MDR, MDD, MPG/MPDG/MPSV, MEDDEV, EN ISO 13485, 21 CFR 820), as well as personal...
Philips International-Böblingen
the right fit if:
• PhD or Medical Degree preferred.
• 10+ years experience in medical/ clinical affairs within medical device/ biotech industry.
• 8+ years of experience leading people through transformation and change management.
• Deep knowledge of...
appcast.io -
Kopani Consulting GmbH-Karlsruhe
naturwissenschaftliches oder technisches Studium
• Grundkenntnisse im Qualitätsmanagement gemäß ISO 13485
• Berufserfahrung im Qualitätsmanagement oder Regulatory Affairs in der Medizintechnik
• Affinität zum digitalem Dokumentenmanagement und sicherer Umgang mit MS...
join.com -
HAPEKO Deutschland GmbH-Tuttlingen
innerhalb der Medizintechnik, bzw. produzierenden Medizinproduktunternehmen
• Gute Kenntnisse in der Anwendung und dem Umgang mit der ISO 13485
• Idealerweise Kenntnisse in den Regularien der Medical Device Regulation / MDR, Medizinprodukteverordnung (2017...
stepstone.de -
PAUL HARTMANN AG-Herbrechtingen
Affairs role within an international company
• Qualification as PRRC according to MDR
• Comprehensive knowledge of the regulatory requirements of medical device (e.g. MDR, MDD, MPG/MPDG/MPSV, MEDDEV, EN ISO 13485, 21 CFR 820), as well as personal...
JOTEC GmbH-Hechingen
Efficiency in managing and motivating direct reports to maximize writers' contributions and career development
• Familiarity with medical devices, MDD and MDR
• Accomplished use of MS Word, PowerPoint and Adobe Acrobat
• Proficiency in written and spoken...
finest-jobs.com -
PAUL HARTMANN AG-Herbrechtingen
Affairs role within an international company
• Qualification as PRRC according to MDR
• Comprehensive knowledge of the regulatory requirements of medical device (e.g. MDR, MDD, MPG/MPDG/MPSV, MEDDEV, EN ISO 13485, 21 CFR 820), as well as personal...
PAUL HARTMANN AG-Herbrechtingen
Affairs role within an international company
• Qualification as PRRC according to MDR
• Comprehensive knowledge of the regulatory requirements of medical device (e.g. MDR, MDD, MPG/MPDG/MPSV, MEDDEV, EN ISO 13485, 21 CFR 820), as well as personal...
PAUL HARTMANN AG-Herbrechtingen
Affairs role within an international company
• Qualification as PRRC according to MDR
• Comprehensive knowledge of the regulatory requirements of medical device (e.g. MDR, MDD, MPG/MPDG/MPSV, MEDDEV, EN ISO 13485, 21 CFR 820), as well as personal...
PAUL HARTMANN AG-Herbrechtingen
evaluation of product-related regulatory requirements
Qualification:
• University degree in science or technical sciences or an equivalent qualification
• Ideally initial professional experience in the medical device environment or another regulatory field...
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