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
Austin Vita is acting as an Employment Agency in relation to this vacancy.
Austin Vita is committed to being an equal opportunities employer, and encourages applications from candidates regardless of sex, race, disability, age, sexual orientation, gender reassignment, religion or belief, marital status, or pregnancy and maternity status.
Due to the volume of applications received, we are unable to provide individual feedback to unsuccessful applicants.