Offer summary
Qualifications:
Bachelor's in a scientific discipline preferred, 5+ years of Regulatory Affairs experience, Experience with complex medical devices, Knowledge of engineering and biology concepts, Familiarity with multiple regulatory frameworks.
Key responsabilities:
- Develop global regulatory strategies to support business
- Lead submissions to regulatory authorities
- Establish processes for meeting regulatory requirements
- Collaborate with teams for regulatory documentation
- Ensure regulatory strategy aligns with commercial goals