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FDA resumes in Castro Valley, CA

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Resume alert Resumes 31 - 40 of 827

Product Manager

Fremont, CA
... • Followed FDA validation guidelines to implement the QSSDV process that improve the quality metrics by 25%. • Formulated Checklists, Engineering practices, Test policies, and workflow processes to implement Verification and Validation methodologies ... - Feb 18

ML Engineer, AI Engineer, Research Engineer

Oakland, CA
... As a Software Verification Tester, I performed 100+ software verification protocols and detailed data analysis to provide data for FDA premarket approval submission and enable use of Class II endometrial ablation device in the clinic. Worked cross ... - Feb 17

Change Management Quality Assurance

San Francisco, CA, 94114
... Extensive experience with managing effective Electronic Quality Management System (eQMS) fulfilling responsibilities based on Quality System Regulation (QSR), ISO 13485:2016, ISO 9001:2015 and FDA Regulations within Medical Device and Pharmaceutical ... - Feb 09

Data Engineer

San Francisco, CA
... • Implemented a chatbot powered by OpenAI and trained on FDA drug data, shaped by insights from user surveys, to provide safe drug suggestions, boosting customer engagement. Graduate Assistant - School of Nursing, SFSU Sep 2023 – Present • ... - Feb 08

Project Management Master Data

Hayward, CA
... Experience in administrating data rules and applications governed under regulatory compliance such as HIPAA, ISO, FDA, SOX, ITAR, EAR, DFAR, and FAR regulations. PROFESSIONAL EXPERIENCE: Data Governance Lead Solo Workforce Consulting 6-2023 -10-2023 ... - Feb 08

Software Engineer C++

Santa Clara, CA, 95050
... • FDA Validation experience with Semiconductor, medical devices and pharmaceutical manufacturing. • Experienced with gas sampling inlets and measuring systems. • Embedded Systems Programming – 80x86 assembler, Forth, C, C++ and C#. • Programming ... - Feb 07

Inventory Control Supply Chain

Fremont, CA
... Expertise in FDA Rules: Manage GMP inventory throughout the SCM, ensure drug accountability Experience of a practical application of U.S and international medical device regulations (IDMRF), FDA, 21 CFR Part 820, ISO 13485, European Device ... - Jan 25

Quality Assurance Document Control

Oakland, CA
... *QI: Verify material's are labled according to build of materials and component formulation (FDA Approved). * Collect and delivery all product at the component level * Complete Documentaion of product that is placed into inventory for back-fill for ... - Jan 25

Supply Chain Vice President

Fremont, CA, 94536
... Adept in major FDA, DEA, EFSA and internal audits. An adroit leader, able to adequately manage the staff of 180+ people. Possess strong decision-making and problem-solving skills needed to identify cost-saving opportunities, lead time compliance, ... - Jan 22

Engineering Technician III

Hayward, CA
Arnold Blanco ad2wjc@r.postjobfree.com • 510-***-**** Senior Technician Technician with 20+ years’ experience in a manufacturing environment with 4 years in Quality Assurance and an extensive background in cGMP, FDA, ISO, Clean Room, and ITAR ... - Jan 18
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