Medical Device Regulatory Associate Jobs
Fujifilm - Boston, Massachusetts
. Performs other duties as assigned by the Area Service Manager. Comply with all applicable U.S. Food and Drug Administration (U.S. FDA) medical device regulatory requirements, applicable ISO 13485 standard
Register your RESUMEfrom: resume-library.com (+1 source) - 3 days ago
Abbott Laboratories - Philadelphia, Pennsylvania
of Ethics and Compliance Quality, Regulatory and others Responsible for exhibiting professional behavior with both internal/external business associates that reflects positively on the company
Register your RESUMEfrom: resume-library.com - 5 days ago
Boston Scientific - Arden Hills, MN, US
, supervisors, and engineers to support manufacturing, new product development, post-market investigations, and Quality Systems for capital equipment and other medical device electronic assemblies. Key tasks
from: Boston Scientific - 21 days ago
Allergan Aesthetics - Irvine, California
in partnership with key medical functional teams; the Associate Director / Director will assist in the development and implementation of comprehensive medical strategies for specific medical devices / products
Register your RESUMEfrom: resume-library.com - 13 days ago
Unisys Corporation - Thousand Oaks, California
Understanding business needs and developing novel yet practical solutions to meet those needs Experience with combination products and device regulatory requirements and medical device development and engineering
Register your RESUMEfrom: resume-library.com - 20 days ago
FUJIFILM Holdings America Corporation - Atlanta, GA
as assigned. Comply with all applicable U.S. Food and Drug Administration (U.S. FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements and all other applicable laws, regulations
from: careerbuilder.com - 4 days ago
Saatchi & Saatchi Wellness - New York County, New York
Job Description The Associate Director, Regulatory Operations is responsible for ensuring regulatory submissions follow the protocols established by our pharmaceutical and medical/surgical device
Register your RESUMEfrom: resume-library.com - 22 days ago
Jobot - Needham, MA (+6 locations)
the biotechnology, pharmaceutical, or medical device industry. Proven experience in clinical trials, including site monitoring, study maintenance, and report writing. Familiarity with regulatory guidelines $120,000 - $130,000/Year
from: careerbuilder.com - 20 days ago
ProClinical - Philadelphia, PA
Associate Director of Regulatory Affairs - Permanent - Onsite Proclinical Staffing is seeking an Associate Director of Regulatory Affairs to join a top medical program. This is a permanent role
from: careerbuilder.com - 11 days ago
Volt - Little Canada, MN
globally based on the spinoff strategy. This is a first shift position. As a Regulatory Affairs Specialist you will be: Redlining medical device labeling based on global requirements per label checklist $39.00 - $39.69/Hour
from: careerbuilder.com - 11 days ago
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