jobid=A.0.0503
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About the Company
A Notified Body in the Netherlands is rapidly expanding their Audit teams due to a large project acquisition. This Notified Body has numerous subsidiaries across Europe and offers world-renowned, fully funded training programs to attain all necessary Certificates.
Key Responsibilities
- Conduct customer audits in accordance with EU requirements and designations
- Create customer evaluation forms and audit reports
- Engage in customer interaction and business development
- Stay up-to-date with current MDD/MDR 2017/745 or IVDR 2017/746 requirements
- Perform conformity assessments of MDR/IVDR for medical devices
- Manage customer complaints
Qualifications
- Successfully completed a Scientific or Engineering degree (BSc/MSc)
- At least 4 years of experience within the Medical Device Industry, with preferred Notified Body experience
- Over 2 years in Research & Development, Quality, or Regulatory roles for Active and/or Non-Active devices
- Knowledge of MDR (2017/745) systems and implementation
- Experience with internal/external audits (preferred)
- Fluent in English and professionally proficient in Dutch
- Excellent verbal and communication skills
Additional Benefits
- Work for a leading Notified Body
- Access to excellent, fully funded training programs
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