ApplyBlast uses AI to match you with the right jobs, tailor your resume and cover letter, and apply automatically so you can land your dream job faster.
© All Rights Reserved. ApplyBlast.com
ApplyBlast uses AI to match you with the right jobs, tailor your resume and cover letter, and apply automatically so you can land your dream job faster.
© All Rights Reserved. ApplyBlast.com
GMED
The role involves managing a portfolio of in‑vitro diagnostic device manufacturers, overseeing the end‑to‑end certification process, ensuring compliance with IVDR and ISO 13485, and serving as the primary liaison between clients and GMED. The position requires coordinating CE marking and quality system certification activities, maintaining regulatory vigilance, and supporting commercial teams as needed.
GMED is a notified body and regulatory conformity partner specializing in certification, conformity assessment, auditing, and training for medical device manufacturers. The firm helps clients navigate regulatory requirements and international standards (including CE marking, ISO 13485 and EU MDR/IVDR pathways), performing assessments, technical reviews, and workshops to support market access. With an international footprint and dedicated regulatory expertise, GMED positions itself as a trusted advisor for health- and innovation-focused medical device companies.
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 GMED.
GMED didn’t post a salary, so this is our estimate from similar listings.
29% below the average for this role