Offer summary
Qualifications:
8-10 years in clinical research/QA, Bachelor’s degree in science or healthcare, Graduate or postgraduate degree preferred, Experience in CRO, pharmaceutical, medical devices, Supervisory experience preferred.Key responsabilities:
- Support audit program for compliance
- Conduct ICH/GCP quality reviews/audits
- Oversee Quality Management Systems and SOPs
- Mentor Quality Compliance team members
- Review documents for FDA submissions