Medical Device Regulatory Affairs Jobs in San Diego, CA

Top Quality Recruitment (TQR) - San Diego, CA, United States

Affairs and/or a science-related field (Required). Master’s degree desired. RAPs RAC strongly preferred Minimum of 10 years of Regulatory Affairs experience within FDA-regulated medical device/technology

from: linkedin.com - 3 days ago

Cypress HCM - San Diego, CA, United States

Regulatory Affairs Specialist The Regulatory Affairs Specialist IV will coordinate the accumulation of technical information and prepare submissions for in vitro diagnostic and medical device

from: linkedin.com - 10 days ago

LanceSoft Inc - San Diego, California

regulatory affairs staff, R&D staff and outside suppliers as required to help define product testing requirements and coordinate with the project team to provide CPDT deliverables. -Serve as Sponsor

from: resume-library.com - 13 days ago

Amerit Consulting - San Diego, CA, United States

, clinical, regulatory, medical affairs, quality, manufacturing, etc. Experience with medical device design control processes and creating and maintaining design control documentation.

from: linkedin.com - 10 days ago

Adecco Permanent Recruitment - San Diego, CA, United States

/MDR requirements. • Represents Regulatory Affairs and Quality team in yearly audits for quality and regulatory documentation including Technical Documentation. • Contributes to Regulatory projects

from: linkedin.com - 4 days ago

Saviance Technologies - San Diego, California

and assessment of compliance. Collaborate with CPDT SMEs, Client project teams, business unit regulatory affairs staff, R&D staff and outside suppliers as required to help define product testing requirements

from: resume-library.com - 13 days ago

Armonica Technologies. Inc. - San Diego, CA, United States

of medical device/diagnostics product development under the QSR process. Understanding of micro/ nanofluidics for manipulation and delivery of long-strand DNA. Deep knowledge of physical and optical phenomena

from: linkedin.com - 11 days ago

Net2Source Inc. - San Diego, CA, United States

regulatory requirements; including review of literature and assessment of compliance. Collaborate with CPDT SMEs, client's project teams, business unit regulatory affairs staff, R&D staff and outside suppliers

from: linkedin.com (+1 source) - 14 days ago

LanceSoft Inc - San Diego, California

to manage multiple projects of varying scopes in parallel • Ability to work leading or as part of a cross-functional team with members from marketing, sales, clinical, regulatory, medical affairs, quality

from: resume-library.com - 25 days ago

Philips - San Diego, CA, US

assignments with minimal supervision. You have a bachelor's degree or equivalent preferably in regulatory affairs or science-related field or equivalent experience in the medical device industry

from: jobvertise.com - More than 30 days ago