Job Description
Job Summary:
- Regulatory affairs role (for this project, looking for someone with at least 5 years direct relevant PMA experience).
- Hands-on experience with authoring, drafting and submitting all modules for a medical device (IVD) PMA – experience with tissues is desired.
- Demonstrated experience working cross functionally (to gather information and collaborate on submission documents).
Additional Job Details:
- Hands-on experience with authoring, drafting and submitting all modules for a medical device (In Vitro Diagnostics) PMA – experience with tissues is desired.