Are you located in Northern LA and looking to advance your regulatory career by working at one of the top class II and III medical device companies specializing in surgical and imaging devices?
If so I'm working on behalf of my client based near Redondo Beach that is urgently looking for a Regulatory Specialist with experience in domestic 510(k) submissions to help with submissions for their class II and III device products.
This role offers the following:
- A competitive base salary and fantastic benefits
- The ability to work on complex submissions for invasive class II and III medical devices
- Work cross functionally with R&D, QA, and senior management to resolve regulatory issues and develop regulatory strategy
Applicants must have:
-A minimum of 3 years of regulatory experience at medical device companies
-Prior experience working on domestic 510(k) submissions
If this seems like a great opportunity for you or someone in your network please reach out as I will be contacting top applicants.
Sthree US is acting as an Employment Agency in relation to this vacancy.