Offer summary
Qualifications:
BS Degree in Sciences or equivalent, 5+ years of regulatory experience., Knowledge of global IVD regulations., Preferred: Master’s degree or Ph.D., Experience with FDA and EU IVDR..Key responsabilities:
- Lead preparation of submissions for approvals.
- Serve as regulatory lead on project teams.
- Represent Precision in agency meetings.
- Design strategies for regulatory clearance.
- Review development protocols and company documents.