03.04.24 | Vollzeit | Wien | JobLeads GmbH | € 100.000 - € 125.000 With the relevant GMP/GDP regulations - Oversee batch release duties and support to the Qualified Person (QP) and Responsible Person (RP) - Drive and oversee that deviations, CAPAs, CCs and other QMS activities are addressed in a GMP/GDP compliant and timely manner - Ensure quality issues are escalated
Später ansehen21.04.24 | Vollzeit | www.gerresheimer.comAnd modified medical devices in different markets. You manage technical guidance and training to the RA team and also cross-functional teams including training on procedures, FDA, MDR guidance documents, and international regulation. Your team take care of various regulatory documents e.g. such as Intended Use
Später ansehen20.04.24 | Vollzeit | Wien, Diesen | Condor Allgemeine Versicherungs AGInformation Security Manager Wien, Österreich Overview Radancy is looking for an Information Security Manager, EU with a deep security and compliance background to lead system development and process improvement efforts. As part of the Radancy’s Governance, Risk, and Compliance (‘GRC’) team
Später ansehen20.04.24 | Vollzeit | Wien | Condor Allgemeine Versicherungs AGInformation Security Manager Vienna, Austria Overview Radancy is looking for an Information Security Manager, EU with a deep security and compliance background to lead system development and process improvement efforts. As part of the Radancy’s Governance, Risk, and Compliance (‘GRC’) team
Später ansehen20.04.24 | Vollzeit | Capelle, Wien | Condor Allgemeine Versicherungs AGInformation Security Manager Capelle aan den IJssel, Netherlands Overview Radancy is looking for an Information Security Manager, EU with a deep security and compliance background to lead system development and process improvement efforts. As part of the Radancy’s Governance, Risk, and Compliance
Später ansehen19.04.24 | Vollzeit | jobs.bd.comYears relevant experience or a combination of equivalent education and relevant experience. Knowledge and Skills - Applied knowledge of the FDA medical device quality system regulations and international quality system standards/regulations (e.g. - 21 CFR Part 820, ISO 13485, ISO 14971, MDSAP, EU MDR
Später ansehen17.01.24 | Vollzeit | JobLeads GmbH | € 125.000 - € 150.000 International product registrations and export certifications as requested by clients and international regulatory agencies in the EU and in third countries. - You perform dossier and development gap analysis (drugs, food supplements) and maintain current technical files and declarations of conformity
Später ansehen29.03.24 | Vollzeit, Teilzeit | luxcara.comWill focus on the following areas - Implementation of ESG strategy aligned with SFDR and EU Taxonomy requirements. - Stay ahead of the latest developments in ESG regulations, guidelines, and best practices. - Conduct comprehensive ESG assessments of investment opportunities and provide insights to support
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