Regulatory Affairs Medical Devices Jobs
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Suchergebnisse - Regulatory Affairs Medical Devices Jobs
PAUL HARTMANN AG-Heidenheim
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...
jobspreader.com -
Humedics GmbH-Berlin
hat.
Zur Verstärkung unseres Teams suchen wir für unsere Zentrale in Berlin
Product / Regulatory Affairs Manager Medical Devices
Werde Teil unseres dynamischen Teams und verhelfe uns dabei, LiMAx weiterzuentwickeln und in Zukunft noch mehr Patienten zu helfen...
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...
Isb Muenchen Immobilien-Münster
Regulatory Affairs, Beratung & Regulatory Affairs, Inspektion, Audit, Hygiene, Qualitätsmanagement / Berufserfahrung, Führungserfahrung
Senior Consultant Regulatory Affairs Pharma (m/w/d) (Münster / München)
Unternehmen/Hintergrund...
appcast.io -
PAUL HARTMANN AG-Heidenheim
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...
jobspreader.com -
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-Heidenheim
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...
jobspreader.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...
Olympus Europa SE & Co. KG-Hamburg
Your competencies include proficiency in MS Word, Excel and PowerPoint
• You have a strong interest in the medical device industry and regulatory affairs
• You have excellent organizational skills and attention to detail
• Good analytical and research...
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...
The Force-Berlin
something – and will give it to you in return.
A TYPICAL DAY TRIP FOR YOU:
• You reside as the interface between R&D, Regulatory Affairs, Marketing and Sales.
• You provide first-class vital Medical Information and compelling scientific dialogue to meet...
appcast.io -
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...
OLYMPUS EUROPA SE & CO. KG-Hamburg
Global Medical Content Manager Scientific Affairs Ecosystems (m/f/d)
• Functioning as medical-scientific subject matter expert and leading the scientific communication for the assigned digital area; liaising with internal cross-functional...
appcast.io -
OmniVision GmbH-Puchheim
portfolio includes pharmaceuticals, medical devices and nutritional supplements.
In the course of our strong growth . click apply for full job details...
PAUL HARTMANN AG-Heidenheim
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...
jobspreader.com -
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