Offer summary
Qualifications:
Master's degree in regulatory affairs or related field, Significant experience in Quality Regulatory Affairs, At least 3 years in medical device/pharmaceutical regulatory affairs, Fluency in English.
Key responsabilities:
- Proactively monitor global regulatory developments
- Assess impact of regulatory intelligence on strategies
- Communicate with internal and external stakeholders
- Collaborate with teams to shape policies
- Build relationships with stakeholders in regulatory affairs