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Regulatory Affairs Medical Devices Jobs in Bayern

1 - 9 von 9
1 - 9 von 9
Suchergebnisse - Regulatory Affairs Medical Devices Jobs in Bayern
OmniVision GmbH-Puchheim-stepstone.de-
affiliated with a corporate group. Our product portfolio includes pharmaceuticals, medical devices, and dietary supplements. Due to our strong growth, we are looking for a dedicated and motivated Manager Regulatory Affairs (m/f/d) to join our headquarters...
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OmniVision GmbH-Puchheim-
ophthalmological companies not affiliated with a corporate group. Our product portfolio includes pharmaceuticals, medical devices, and dietary supplements. /n Due to our strong growth, we are looking for a dedicated and motivated /n Manager Regulatory Affairs...
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Abbott Laboratories-München-jobs.abbott-
and modules, focused on CE and FDA regulatory pathways for medical device software  •  Contribute to key regulatory areas such as technical documentation, clinical evaluation, and safety reports  •  Lead risk management activities throughout the product lifecycle...
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OmniVision GmbH-Puchheim-joblookup.com-
ophthalmological companies not affiliated with a corporate group. Our product portfolio includes pharmaceuticals, medical devices, and dietary supplements. xdhcjke Lesen Sie weiter, um sich ein umfassendes Bild von dieser Stelle zu machen und zu erfahren...
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PAUL HARTMANN AG-Heidenheim-
and go-to-market strategies  •  Maintain the current portfolio  •  Collaborate with R&D, Market Access, Regulatory Affairs and commercial teams worldwide  •  Manage international cross-functional projects and stakeholder networks  •  Deliver product and portfolio...
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OmniVision GmbH-Puchheim-my-perfect-job.de-
affiliated with a corporate group. Our product portfolio includes pharmaceuticals, medical devices, and dietary supplements. Due to our strong growth, we are looking for a dedicated and motivated Manager Regulatory Affairs (m/f/d) to join our headquarters...
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Roche-Penzberg-roche.com-
professional experience in Regulatory Affairs, R&D, or Clinical Development within the IVD, medical device, or biopharmaceutical industries (typically 5–8 years depending on degree level).  •  Regulatory Expertise: In-depth knowledge of international laws...
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München-medpace.com-
Clinical Safety Coordinators on safety reporting responsibilities  •  Coordinate safety responsibilities for aggregate reporting purposes (e.g., ensure timely data entry, tracking of pending cases, collaborate with Medical Monitor and Regulatory Affairs...
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Roche-Penzberg-roche.com-
experience in Regulatory, R&D, Quality, Operations or Clinical  •  Technical understanding of medical devices or IVDs  •  Knowledge in international laws and regulations for development, manufacturing and registration of IVDs especially in EU, US and China...
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