As a Consultant Medical Devices, you will focus on developing, implementing, and improving quality systems within the medical device industry. You will support clients in meeting standards such as ISO 13485, ISO 9001, ISO 14971, and the current medical device legislation (MDR/IVDR).
Requirements
- Familiarity with ISO 13485 and possibly also with ISO 9001, ISO 14971, MDR, and/or IVDR.
- Experience in evaluating, setting up, and optimizing processes and procedures.
- Knowledge of risk management and guiding and/or preparing technical and process documentation.
- Analytical, result-oriented, and pragmatic with strong communication skills.
- Ability to switch between English and Dutch in writing and speech.
Benefits
- Salary between €3,500 - €4,500 on a full-time basis
- Lease car or mobility allowance
- Training and certification opportunities
- Pension scheme
- Smartphone and laptop
- 28 vacation days
- Home working allowance
- Disability insurance