Lead Auditor Medical Devices
vor 1 Woche
Your primary tasks will include: Planning and Conducting international Audits under ISO 13485, MDR and MDSAP Conducting Technical Documentation assessments per competence profile. Documenting Audit results per Accreditation / Designation requirements. Develop and support the company culture within the Audit department Responsible for reporting to the Audit Team Leader DNV is an Equal Opportunity Employer and gives consideration for employment to qualified applicants without regard to gender, religion, race, national or ethnic origin, cultural background, social group, disability, sexual orientation, gender identity, marital status, age or political opinion. Diversity is fundamental to our culture and we invite you to be part of this diversity. An academic degree in Engineering or any Natural ScienceAt least 4 years work experience in the design, manufacturing, testing or application of medical devicesKnowledge of quality management system certification and regulatory requirements for CE-markingGood communication skills (German and English)Ability to initiate and maintain cross-cultural collaboration"Please note that we cannot proceed to the interview stage without the following documents: Curriculum Vitae (CV); Cover- /Motivation Letter; University Diplomas & Transcripts; Reference Letter(s). All documents shall preferably be submitted in English. Please provide them at your earliest convenience to ensure a smooth and timely assessment process. Your cooperation in this matter is greatly appreciated.”
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Lead Auditor Medical Devices
Vor 2 Tagen
Hamburg, Hamburg, Deutschland DNV Vollzeit 60.000 € - 120.000 € pro JahrDescriptionYour primary tasks will include:Planning and Conducting international Audits under ISO 13485, MDR and MDSAPConducting Technical Documentation assessments per competence profile.Documenting Audit results per Accreditation / Designation requirements.Develop and support the company culture within the Audit departmentResponsible for reporting to the...
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Lead Auditor Medical Devices
Vor 2 Tagen
Hamburg, Deutschland DNV VollzeitYour primary tasks will include: - Planning and Conducting international Audits under ISO 13485, MDR and MDSAP - Conducting Technical Documentation assessments per competence profile. - Documenting Audit results per Accreditation / Designation requirements. - Develop and support the company culture within the Audit department - Responsible for reporting to...
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Auditor in Zur Qualifikation Als Lead Auditor in
vor 1 Woche
Hamburg, Deutschland TÜV SÜD Management Service GmbH VollzeitSeit 1866 gilt unsere Leidenschaft der Technik und der Sicherheit. Innovationen beeinflussen unser Leben in vielfältiger Weise. Für die Sicherheit von Menschen und der Gesellschaft setzen wir uns jeden Tag aufs Neue ein und schaffen Vertrauen in neue Technologien. Wir sind Teil des Fortschritts. Wir beraten, wir prüfen, wir zertifizieren. Wir handeln aus...
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Medical Affairs Lead
Vor 7 Tagen
Greater Hamburg Area, Deutschland seca – precision for health Vollzeit 80.000 € - 120.000 € pro JahrWe firmly believe that the safety and well-being of patients are the highest values when it comes to healthcare. Ensuring these begins with the smallest details – every gram, every millimeter, every decimal point, and every single heartbeat. When it comes to medical evaluations and decisions, there is no such thing as "approximately" or "roughly."That's...
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Intern Medical Devices
Vor 2 Tagen
Hamburg, Deutschland NSF International VollzeitNSF Prosystem is looking for a new intern to join their team. - Responsibilities: Creation, maintenance, and updating of technical documentation for national and international registration projects - Development and enhancement of quality management systems - Preparation of clinical evaluations - Intensive work with national and international regulations and...
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Hamburg, Deutschland D.Med Consulting GmbH VollzeitYour responsibilities: Conducting regulatory GAP analyses and overseeing the interpretation and integration of applicable global regulatory requirements for medical devices into internal processes Creating, reviewing, and maintaining high-quality technical documentation in compliance with MDR, IVDR, and other relevant standards Developing and managing market...
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Lead Auditor*in
vor 1 Tag
Hamburg, Deutschland SGS VollzeitStellenbeschreibungPlanung, Durchführung und Nachbereitung von externen Audits bei unseren KundenDokumentation im Rahmen der Akkreditierungsvorgaben und der SGS-internen Regularien sowie die Erstellung von Auditberichtengezielte Weiterentwicklung zum Lead Auditor*in in weiteren Standards für die weltweit marktführende...
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Lead Auditor In-vitro Diagnostics
Vor 7 Tagen
Hamburg, Hamburg, Deutschland DNV Vollzeit 60.000 € - 90.000 € pro JahrYour primary tasks will include:Planning and Conducting international Audits under ISO 13485, MDR or IVDR and MDSAPConducting Technical Documentation assessments per competence profile.Documenting Audit results per Accreditation / Designation requirements.Develop and support the company culture within the Audit departmentResponsible for reporting to the...
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Engineer, Product Applications
vor 1 Woche
Hamburg, Hamburg, Deutschland Analog Devices Vollzeit 65.000 € - 85.000 € pro JahrCome join Analog Devices (ADI) – a place where Innovation meets Impact. For more than 55 years, Analog Devices has been inventing new breakthrough technologies that transform lives. At ADI you will work alongside the brightest minds to collaborate on solving complex problems that matter from autonomous vehicles, drones and factories to augmented reality...
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Teamleiter Life Supporting Devices
Vor 7 Tagen
Hamburg, Deutschland Löwenstein Medical SE & Co. KG Vollzeit**Teamleiter Life Supporting Devices (m/w/d) Lifecycle Management Medizintechnik**: - Hamburg **Warum Löwenstein Medical Technology?**: **Neue Wege gehen.**Aber nie vergessen, wo man herkommt. Löwenstein Medical Technology ist ein mittelständisches Unternehmen unter dem Dach der international aufgestellten Löwenstein Gruppe. Als Kompetenzträger für...
