Latest Medical Device Regulatory Affairs jobs in Santa Clara, CA

20 Medical Device Regulatory Affairs Jobs in Santa Clara, CA

Regulatory Affairs Specialist 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 9 days ago
Regulatory Affairs Specialist 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 18 days ago
Medical Device Quality Engineer I 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 Yesterday
Associate Quality Engineer Bayside Solutions - Santa Clara, CA, United States in conjunction with Regulatory Affairs. Investigate and review medical device complaints to help identify root causes, solutions, and trends. Perform risk assessments. Write protocols and reports for activities 25 days ago
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Senior Regulatory Affairs Specialist - Vascular (on-site) Abbott Laboratories - Santa Clara, California industry. Certification is a plus (such as RAC from the Regulatory Affairs Professionals Society.) * Participants who complete a short wellness assessment qualify for FREE coverage in our HIP PPO medical 6 days ago
Regulatory Specialist II The Fountain Group LLC - Santa Clara, California for the position are as follows: Pay: $60-56 Experience: 2-5 years regulatory experience and/or 2 years relevant industrial experience typically with a quality, product-development/support, or scientific affairs 25 days ago
Regulatory Affairs (HCLA49) 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 More than 30 days ago
Sr Quality Manager, BioProcess Equipment and Automation Thermo Fisher Scientific - Santa Clara, CA of bioprocessing technology and capabilities, pharmaceutical production, pharmaceutical new product or medical device introductions Knowledge of project-based manufacturing processes including capital 25 days ago
IT Project Manager (HCLA54) HCL America, Inc. - Santa Clara, CA, US to finalize product requirement gaps with respect to new Medical Device Regulations (MDR). Develop remediation plans. Roll out project strategy and schedules through a formal kickoff meeting. Initiate process More than 30 days ago
Regulatory Affairs Manager EPM Scientific - San Jose, CA, United States Title: Regulatory Affairs Manager Location: San Jose, CA Base Salary: $140,000-$190,000 About: Currently working with a medical device company dedicated to developing and commercializing breakthrough 23 days ago

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