Regulatory Affairs Specialist
vor 1 Woche
Chameleon International Search Ltd is partnering with a leading Medical Device organisation to fill a critical role in their Regulatory Affairs and Quality Management team.
The company is a well-established international group with a strong presence in Europe and Asia, known for their innovative approach to product research and development and their entrepreneurial spirit.
This role will be responsible for overseeing the Quality Systems and Regulatory Affairs function for the company's German-based subsidiary, with a focus on:
- Ensuring compliance with legal and regulatory requirements for medical devices under the Medical Device Regulation (MDR)
- Developing and implementing effective quality management systems
- Collaborating with cross-functional teams to drive business growth and innovation
The ideal candidate will have:
- Experience in class 3 medical devices
- In-depth knowledge of MDR and related regulations
- Excellent English and German language skills
This is an exciting opportunity for a seasoned professional to join a dynamic team and contribute to the company's continued success.
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