medical devices in both the U.S. and Europe, support of international product registrations and related regulatory affairs...Responsibilities: This position is responsible for the preparation of regulatory submissions required to market...
Responsibilities: Responsibilities include developing regulatory strategies, reviewing design input/output... documentation, identification of applicable standards and guidance documents, performing regulatory assessments to determine the...
years’ experience working with Class II, Class III medical devices and/or biologics/drugs. Regulatory Affairs Certification... Specialist –Business Partnerships will work on-site out of our Alameda, CA location in the Diabetes Care Division. We’re focused...