DescriptionYour 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
ResponsibilitiesDNV 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.
Qualifications- An academic degree in Engineering or any Natural Science
- At least 4 years work experience in the design manufacturing testing or application of medical devices
- Knowledge of quality management system certification and regulatory requirements for CEmarking
- Good communication skills (German and English)
- Ability to initiate and maintain crosscultural 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.