Required Qualifications:
- Bachelor's degree required.
- 1–3 years of relevant experience.
- Medical Device Reporting (MDR) experience.
- Complaint handling experience.
- Knowledge of regulatory compliance.
- Strong analytical and critical thinking skills.
- Excellent organizational and time management skills.
- Strong written communication.
- Attention to detail.
- Ability to manage multiple priorities.
- Medical device industry experience.
Preferred Qualifications:
- Clinical background (RN or Healthcare Professional).
- Biomedical Engineering background.
- Experience in a regulated environment.
- Knowledge of quality systems.
- Experience with adverse event reporting.
- Cross-functional collaboration experience.