REVA Medical
The Regulatory Affairs Specialist serves as a key regulatory expert for US, EU, and regional filings, providing strategic guidance on complex medical devices and post-market changes. This role involves preparing global regulatory submissions, leading interactions with government entities like the FDA, and ensuring compliance with international quality standards. The specialist collaborates with cross-functional teams to drive product development and resolve regulatory issues.
REVA Medical is a leader in bioresorbable polymer technologies for vascular applications, developing and selling implantable medical devices to restore patient health. The company's product portfolio includes the MOTIV Bioresorbable Scaffold for below-the-knee peripheral artery disease (CE Mark approved, FDA Breakthrough Technology), TyroSphere embolic microspheres for hypervascular tumors, and the Fantom Encore bioresorbable scaffold, all built on REVA's proprietary Tyrocore polymer. Headquartered in San Diego, CA, REVA Medical operates in the implantable medical device industry.
Headquarters
San Francisco, CA
Company Size
201-500 employees
Founded
2018
Industry
Technology
Glassdoor Rating
4.2 / 5
Sarah Johnson
Chief Executive Officer
Michael Chen
Chief Technology Officer
Emily Williams
VP of Engineering
David Rodriguez
VP of Product
Jessica Thompson
Chief Financial Officer
Andrew Park
VP of Sales
View leadership team, funding history,
and employee contacts for REVA Medical.
29% below the average for this role