Übersicht
Principal Regulatory Affairs specialist with strong SaMD (IEC 62304), Class II and III Medical Device experience interested in working for an early stage start-up creating pioneering life saving technologies are encouraged to apply.
A) Here are some of the things you'll be doing:
- Drafting and executing FDA submissions for medical devices (including Class III) and devices incorporating hardware and software.
- Working with external regulatory consultants to implement regulatory strategy.
B) You will be rewarded with:
- A competitive compensation package
- A very competitive equity package
- Generous benefits
