Offer summary
Qualifications:
Bachelor's degree in Science or Engineering, Five years experience with medical devices, Strong understanding of Safety and EMC Standards, Good understanding of ISO standards, Knowledge of global medical device regulations.
Key responsabilities:
- Provide regulatory support for product life cycle.
- Lead teams on regulatory submissions and compliance.
- Identify risks and develop mitigation strategies.
- Ensure timely review of labeling and claims.
- Drive continuous improvement initiatives.