Vakante Jobangebote finden Sie unter Projekte.
Senior Regulatory Affairs Specialist - $140,000 - South Bay
Eingestellt von Real Staffing Group aus Frankfurt am Main
Projektbeschreibung
The following responsibilities will be at the center of the job:
* Drive the process and submission of an IDE and a 510(K)
* Communicate regularly with the FDA
* Serve as regulatory affairs lead for key product development teams
* Keep senior management informed in the regulatory process and strategies
* Write, compile and submit regulatory documentation to global health agencies for approval/clearance
We are looking for candidates who:
* Have exceptional writing skills and attention to detail
* Have played a major role in leading a 510(K) clearance or IDE submission
* Have a bachelors degree
* Have a minimum of 3-5 years of regulatory affairs experience in the medical device industry
* If the candidate is more experienced and has managed others, s/he may come in at the manager level
* Have a passion for revolutionary technology
* Will embrace the company culture, spirit, and commitment
To find out more about Real please visit www.realstaffing.com
Projektdetails
-
Einsatzort:
San Jose, California, Vereinigte Staaten
-
Projektbeginn:
asap
-
Projektdauer:
Keine Angabe
- Vertragsart:
-
Berufserfahrung:
Keine Angabe
Geforderte Qualifikationen
-
Kategorie:
Sonstiges