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Internal auditor Jobs in Ludwigsburg
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Internal auditor • ludwigsburg
- Gesponsert
Medical Auditor
Strativ GroupStuttgart, DE- Gesponsert
IT Auditor (m / w / d)
MANN+HUMMEL GmbHLudwigsburgSenior IT Auditor (m / w / d)
SyntegonWaiblingen- Gesponsert
Senior Auditor Quality Assurance Manager (m / f / x)
SciProBaden-Württemberg, Germany, Germany- Gesponsert
Auditor
SymBio.Stuttgart, DE(Senior) Consultant Internal Auditor IT - Financial Services (w / m / d) - Consulting, IT-Security, Ingenieur
EY (Ernst & Young GmbH)Stuttgart, Germany- Neu!
Auditor •in Entsorgungswirtschaft (w / m / d)
TÜV Rheinland GroupStuttgart, Baden-Württemberg, DEAuditor - Internal Audits
Eberspächer GroupBaden-Württemberg, DE- Gesponsert
Quality Auditor
Life Science PeopleStuttgart, DEIT-Auditor (m / w / d) in Stuttgart
Grühn GmbHStuttgart, Baden-Württemberg, DE(Junior-) Auditor (m / w / d)
DEKRA Assurance Services GmbHStuttgart, DESenior Internal Auditor (m / w / d) Interne Revision
Alfred Kärcher SE & Co. KGWinnenden, DEAuditor / in ISO 9001, ISO 14001, ISO 27001 (Region Stuttgart, München) als Freelancer
DIQZ | Deutsches Institut für Qualität & Zertifizierung GmbHStuttgart, Baden-Württemberg, DEInitiativbewerbung - Internal Functions
LIGANOVAStuttgartIT Auditor (m / f / d)
MAHLEStuttgart, DE- Gesponsert
Junior Internal Auditor (m / w / d)
Dürr AGBietigheim-BissingenIT Auditor (m / w / d).
MANN+HUMMELLudwigsburgInformation Technology Governance Manager
Barclay SimpsonStuttgart, Baden-Württemberg, DEInternal Auditor / Revisor (m / w / d)
JYSKStuttgart, BW, DEMedical Auditor
Strativ GroupStuttgart, DEMedical Device Assessor (Germany – Remote)
50% Auditing | 50% Technical Documentation Reviews
Join a Growing German Notified Body
We are expanding our Medical Device team and seeking experienced professionals to join a German Notified Body in a fully remote capacity. This is a unique opportunity to be at the forefront of European medical device regulation, contributing both through onsite / remote audits and technical documentation reviews for CE certification under MDR 2017 / 745 .
This role offers an ideal balance between field-facing auditing and in-depth file assessments, suited to individuals who want to make a meaningful impact on patient safety and product compliance.
What You'll Do
- Conduct audits under ISO 13485 , MDR , and MDSAP , either remotely or on-site (limited travel)
- Review Technical Documentation for active and non-active medical devices in line with MDR Annex II and III
- Evaluate design dossiers, clinical evaluations, risk management, and sterilization processes
- Prepare detailed assessment reports and issue certification recommendations
- Collaborate with internal medical and regulatory teams on conformity assessments
- Support clients through the certification process with clear, structured feedback
- Maintain regulatory knowledge and participate in continuous internal training
What You’ll Bring
What’s Offered
Ready to join?
Apply with your CV in English and become part of a team ensuring medical devices meet the highest regulatory and safety standards.