Offer summary
Qualifications:
University Degree or advanced degree, Minimum 4 years relevant experience, ISO 13485 experience required, Experience with 21 CFR part 820/821 and EU 2017/745, Familiarity with CAPA, PFMEA and FMEA.
Key responsabilities:
- Coordinate and prepare regulatory submissions and document packages
- Recommend changes for compliance in labeling, manufacturing, and marketing
- Manage projects from design to implementation with minimal supervision
- Provide mentoring and training to lower level specialists
- Communicate effectively with internal and external stakeholders