| Resume alert | Resumes 21 - 30 of 743 |
Supply Chain Management
San Jose, CA, 95127
... Built and loaded projected Growth plans and New Product Introduction cut-in forecasts for $1 billion+ business plans, including FDA and GMP Procedures, and Spares/Field Service coverage. Management of 8+ key customer accounts and over $300 million ... - Feb 22
... Built and loaded projected Growth plans and New Product Introduction cut-in forecasts for $1 billion+ business plans, including FDA and GMP Procedures, and Spares/Field Service coverage. Management of 8+ key customer accounts and over $300 million ... - Feb 22
Medical Device Quality Control
Hillside, CA, 95030
... orderly and thorough data collection ●Trained to follow Good Manufacturing Practices (GMP), ISO 13485:2016, ISO 9001:2008, FDA 21 CFR 820 ●Detail-oriented, self-motivated team player, and capable of training other associates ●Ability to quickly ... - Feb 19
... orderly and thorough data collection ●Trained to follow Good Manufacturing Practices (GMP), ISO 13485:2016, ISO 9001:2008, FDA 21 CFR 820 ●Detail-oriented, self-motivated team player, and capable of training other associates ●Ability to quickly ... - Feb 19
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
... • 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
... 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
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
... 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 Web Server
Sunnyvale, CA, 94086
... • Strong programming, development and scripting background • Experience with ISO and FDA standards qualification processes • Self motivated, hard worker, quicker learner, leader and team player Languages HTML, DHTML, CSS, JavaScript, AJAX, FLEX, XML ... - Feb 08
... • Strong programming, development and scripting background • Experience with ISO and FDA standards qualification processes • Self motivated, hard worker, quicker learner, leader and team player Languages HTML, DHTML, CSS, JavaScript, AJAX, FLEX, XML ... - 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
... • 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
Technical Writer Senior
San Jose, CA, 95113
... Also, ensure that documentation properly conforms to all applicable Philips, FDA, and international regulatory requirements. Experience Senior Technical Writer (Contract), Engineering Services June 2013-March 2014 Blue Coat Systems, Inc., Sunnyvale, ... - Feb 07
... Also, ensure that documentation properly conforms to all applicable Philips, FDA, and international regulatory requirements. Experience Senior Technical Writer (Contract), Engineering Services June 2013-March 2014 Blue Coat Systems, Inc., Sunnyvale, ... - Feb 07
Technical Writer Instructional Designer
Los Gatos, CA
... in consumer journalism, promotional, and feature writing for newspapers and magazines Technical Skills: Medical Devices/FDA UX/UI Documentation Enterprise Software Virtualization and SaaS Telecommunications SAP and EtQ Experience Semiconductor ... - Jan 28
... in consumer journalism, promotional, and feature writing for newspapers and magazines Technical Skills: Medical Devices/FDA UX/UI Documentation Enterprise Software Virtualization and SaaS Telecommunications SAP and EtQ Experience Semiconductor ... - Jan 28
Supply Chain Procurement Manager
San Jose, CA
... expired raw materials by 18% • Established local strategic sourcing options & negotiate favorable pricing, which meet FDA requirements • Communicated weekly presentations ensuring of material usage resulting in cost savings and reduced waste • ... - Jan 25
... expired raw materials by 18% • Established local strategic sourcing options & negotiate favorable pricing, which meet FDA requirements • Communicated weekly presentations ensuring of material usage resulting in cost savings and reduced waste • ... - Jan 25