Regulatory Affairs Medical Devices Jobs in Rheinland-Pfalz
1 - 14 von 14
Suchergebnisse - Regulatory Affairs Medical Devices Jobs in Rheinland-Pfalz
Lohmann GmbH & Co. KG-Neuwied
m/w/d) mit zusätzlicher Weiterbildung als Regulatory Affairs Manager oder vergleichbare Qualifikation
• Kenntnisse und Erfahrung im Umgang mit den gängigen Normen (EN ISO 13485, DIN EN ISO 14971,…).
• Mind. 5 Jahre Berufserfahrung im Bereich Regulatory Affairs
• Erste...
stepstone.de -
SCHOTT AG-Bad Kreuznach
preferred
• 5-10 years of professional experience in regulatory affairs or medical devices, with a focus on interfaces with quality management
• Profound knowledge of the regulatory framework for parenteral packaging, combination products, and medical...
SCC Scientific Consulting Company GmbH-Bad Kreuznach
Our passion: managing registration and approval procedures for agrochemicals and biorationals, chemicals, biocides as well as pharmaceuticals and medical devices. Our goal: to grow even further and to open up new areas of business in an international...
appcast.io -
SCHOTT AG-Mainz
preferred
• 5-10 years of professional experience in regulatory affairs or medical devices, with a focus on interfaces with quality management
• Profound knowledge of the regulatory framework for parenteral packaging, combination products, and medical...
SCHOTT AG-Ingelheim am Rhein
preferred
• 5-10 years of professional experience in regulatory affairs or medical devices, with a focus on interfaces with quality management
• Profound knowledge of the regulatory framework for parenteral packaging, combination products, and medical...
Lohmann GmbH & Co. KG-Neuwied
und Lieferantenaudits
• Mitarbeit bei Produktentwicklungsprojekten, insbesondere bei Aufbau und Erstellung der Inhalte und Struktur der technischen Dokumentation, insbesondere der Risikoma-nagement-Akte (DIN EN ISO 14971)
• Enge Zusammenarbeit mit Regulatory Affairs...
stepstone.de -
SCHOTT AG-Ingelheim am Rhein
preferred
• 5-10 years of professional experience in regulatory affairs or medical devices, with a focus on interfaces with quality management
• Profound knowledge of the regulatory framework for parenteral packaging, combination products, and medical...
SCHOTT AG-Rheinland-Pfalz
preferred
• 5-10 years of professional experience in regulatory affairs or medical devices, with a focus on interfaces with quality management
• Profound knowledge of the regulatory framework for parenteral packaging, combination products, and medical...
SCHOTT AG-Mainz
preferred
• 5-10 years of professional experience in regulatory affairs or medical devices, with a focus on interfaces with quality management
• Profound knowledge of the regulatory framework for parenteral packaging, combination products, and medical...
AbbVie-Ludwigshafen am Rhein
improvement
• Represent the PDS&T group in cross functional business teams including Operations, Planning, Purchasing, Quality, Process Sciences, Regulatory Affairs, and Marketing to design, select, develop, test, and commercialize new packaging components...
surfingwave.app -
SCHOTT AG-Ingelheim am Rhein
preferred
• 5-10 years of professional experience in regulatory affairs or medical devices, with a focus on interfaces with quality management
• Profound knowledge of the regulatory framework for parenteral packaging, combination products, and medical...
SCHOTT AG-Bingen am Rhein
preferred
• 5-10 years of professional experience in regulatory affairs or medical devices, with a focus on interfaces with quality management
• Profound knowledge of the regulatory framework for parenteral packaging, combination products, and medical...
SCHOTT AG-Mainz
preferred
• 5-10 years of professional experience in regulatory affairs or medical devices, with a focus on interfaces with quality management
• Profound knowledge of the regulatory framework for parenteral packaging, combination products, and medical...
SCHOTT AG-Bad Kreuznach
preferred
• 5-10 years of professional experience in regulatory affairs or medical devices, with a focus on interfaces with quality management
• Profound knowledge of the regulatory framework for parenteral packaging, combination products, and medical...
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