Medical Device Regulatory Affairs Jobs in Santa Clara, CA
GForce Life Sciences - Santa Clara, CA, United States
of regulatory strategy and priorities in conjunction with management, peers, and commercial, and affiliate personnel in the medical device industry. Key Responsibilities: Duties: Assist in the definition
from: linkedin.com - 6 days ago
GForce Life Sciences - Santa Clara, CA, United States
Regulatory Affairs Specialist II – Santa Clara, CA Must be able to work on a W2 Job Summary We're looking for a Regulatory Specialist with 2-5 years of experience in the medical device industry
from: linkedin.com - 22 days ago
Placement Services USA, Inc. - Santa Clara, CA, US
and regulatory teams to implement design documents and labeling updates. Work with labeling function for the labeling artwork, translations, and release. Work with Global Medical Affairs to develop clinical
from: jobvertise.com - 10 days ago
Anatomage, Inc. - Santa Clara, California
We Look For Experience with Medical Device Software and Hardware Experience with QMS/eQMS Knowledge of ISO 13485 / MDSAP Global regulatory affairs experience (FDA, MDD/CE/MDR, UKCA, etc.) Document Control
Register your RESUMEfrom: resume-library.com - 14 days ago
Johnson and Johnson - Santa Clara, CA
and partnership with R&D, Global Strategic Marketing, Regulatory Affairs, Clinical Engineering, Supply Chain, Quality and Finance. The role also requires strong technical expertise in Class II, III medical device
from: Johnson and Johnson (+1 source) - 10 days ago
Thermo Fisher Scientific - Santa Clara, California, United States of America
Competency of bioprocessing technology and capabilities, pharmaceutical production, pharmaceutical new product or medical device introductions Knowledge of project-based manufacturing processes including
from: jobs.thermofisher.com - 17 days ago
HCL America, Inc. - Santa Clara, CA, US
Location: Santa Clara, CA and various unanticipated locations throughout the U.S. Job Title: Lead Regulatory Affairs (HCLA49) Multiple positions available Job Description: Provide regulatory
from: jobvertise.com - More than 30 days ago
Sunnyvale, CA
, and groundbreaking devices like Fire tablets, Fire TV and Echo Frames. Working as part of the Medical Devices Operational Compliance Team (MD-OCC), the Sr. Regulatory Affairs Specialist will be working to build best
from: Pharmadiversityjobboard.com - 27 days ago
Octave - Menlo Park, CA, United States
opportunities for differentiation and growth within the medical device and diagnostics landscape. Cross-Functional Collaboration: Work closely with sales, product development, regulatory affairs, finance, partner
from: linkedin.com - 8 days ago
Providence Medical Technology, Inc. - Pleasanton, CA, United States
and competitive analysis to identify trends, gaps, and opportunities in the spine medical device sector. Assist in developing and implementing strategic product plans and roadmaps to address market needs. Product
from: linkedin.com - 25 days ago
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