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Corporate auditor Jobs in Düsseldorf
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Corporate auditor • dusseldorf
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Medical Auditor
Strativ GroupDüsseldorf, DENight Auditor (m / w / d)
25hours Hotel Köln The CircleKöln, Germany- Gesponsert
Experienced IT-Auditor (m / w / d)
MediaMarktSaturnDüsseldorf(Senior) Executive Corporate Communications (mensch)
Omnicom Media GroupDüsseldorf, Nordrhein-Westfalen, DeutschlandPraktikum / Praktikant - Corporate Finance / M&A
Corporate Finance Mittelstandsberatung GmbH (CF-MB)Düsseldorf, North Rhine-Westphalia, GermanyCorporate Controller wmd
Deutsche GlasfaserDüsseldorf, North Rhine-Westphalia, GermanyNight Auditor (m / w / d)
The Deutz Tribute Portfolio by MarriottKöln, GermanyNight Auditor / Nachtportier (m / w / d)
Mercure Hotel Köln City FriesenstraßeKöln, GermanyPraktikum Corporate Identity & Design
Lidl Stiftung & Co KGDüsseldorf, DE- Gesponsert
Quality Auditor
Life Science PeopleDüsseldorf, DE- Gesponsert
Energiebeauftragter / Interner Auditor (m / w / d)
Kloeckner Metals Germany GmbHDüsseldorf, DEAuditor Actuarial (m / w / d)
ERGO Group AGDüsseldorf, NW, DE- Gesponsert
Auditor
SymBio.Düsseldorf, DE- Gesponsert
Corporate Associate
Goodman MassonDüsseldorf, Germany- Gesponsert
Environment, Health and Safety Manager
Yanfeng USA Automotive Trim Systems Inc.Neuss, North Rhine-Westphalia, GermanyAssistant Auditor (m / w / d)
KBHT Kalus + Hilger PartG mbBNeuss, Nordrhein-Westfalen, Deutschland- Gesponsert
Auditor zur Qualifikation als Lead Auditor mit Schwerpunkt Informationssicherheit ISO IEC 27001 / TISAX (w / m / d)
TÜV SÜD AGDüsseldorf, DECorporate German Trainer
goFLUENTDüsseldorf, DE(Junior) IT-Auditor (m / w / d)
Flossbach von Storch SEKöln, GermanyMedical Auditor
Strativ GroupDüsseldorf, 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.