Passionate about regulatory affairs? Join us as a Regulatory Affairs specialist. You'll shape compliance for IVD products and research items, support documentation creation, and drive regulatory success.
Your Role:
- Implement vital regulatory standards.
- Craft compliant technical documents.
- Aid in performance evaluation documentation.
- Support clinical studies records.
- Ensure label and marketing compliance.
- Contribute to new approval dossiers.
What You Offer:
- Regulatory insights for IVD and research.
- Strong documentation skills.
- Detail-oriented approach.
- Collaborative mindset.
