Internal auditor Jobs in Bochum
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Internal auditor • bochum
- Gesponsert
Medical Auditor
Strativ GroupEssen, DE- Gesponsert
Senior Auditor (m / w / divers)
thyssenkrupp AGEssenAuditor : in / Produktmanager : in ISO 19443 (QMS in Nuklear-Branche) (m / w / d) - Projektmanagement, IT
TÜV NORD GROUPEssen, DEFlex Quality Auditor with Dutch (m / f / d)
TELUS InternationalEssen, DEAI Quality Auditor with Turkish
TELUS DigitalEssen, North-Rhine-Westphalia, Germany- Gesponsert
Wirtschaftsprüfer / Executive Auditor (m / w / d) - Financial Services
Genoverband e.V.Nordrhein-Westfalen, GermanySenior Auditor Trading (m / f / t) & Commercial Audits
RWE AGEssen, NW, DE, 45141Quality Auditor with Hebrew (m / f / d)
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ArcadisEssen, Nordrhein-Westfalen, Germany- Gesponsert
IT Auditor •in ISMS zur Weiterqualifizierung als Lead Auditor •in
TÜV SÜD AGEssen, DE- Gesponsert
Internal Sales Mitarbeiter (m / w / d)
gym80 International GmbHGelsenkirchen, Nordrhein-Westfalen, GermanyAuditor •in TISAX (w / m / d)
TÜV RheinlandEssen- Gesponsert
Quality Auditor
Life Science PeopleEssen, DE- Gesponsert
Auditor zur Qualifikation als Lead Auditor mit Schwerpunkt Informationssicherheit ISO IEC 27001 / TISAX (w / m / d) - IT-Security, Ingenieur
TÜV SÜDEssen, GermanySenior Consultant Cyber Security / IT Security (m / w / d)
carmasecEssen, DEInternal Audit Manager (m / w / d)
BrenntagEssen, Germany- Gesponsert
Auditor
SymBio.Essen, DEFachreferent Revision Technik / Bau m / w / d
tritec pro eine Marke der TriTec Hr GmbHEssen, Ruhr- Gesponsert
Deputy Specialist Manager : in im Bereich Automotive
TÜV NORD CERT GmbHEssen, Nordrhein-Westfalen, GermanyMedical Auditor
Strativ GroupEssen, 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.