| Resume alert | Resumes 11 - 20 of 574 |
Quality Systems Biomedical Engineering
Milpitas, CA
... • Experimented and contributed with writing a document on biomedical product requirement specification in accordance with FDA regulations, standards, and the Code of Federal Regulations (CFR). • Evaluated and analyzed information obtained from FDA ... - Mar 17
... • Experimented and contributed with writing a document on biomedical product requirement specification in accordance with FDA regulations, standards, and the Code of Federal Regulations (CFR). • Evaluated and analyzed information obtained from FDA ... - Mar 17
Desktop Support Administrator, IT Support Specialist, Tech Support
Pleasanton, CA
... Worked closely with the Quality and Regulatory team, during the FDA audit. Monitored and maintained Help Desk tickets in the Remedy system. Imaged and deployed refurbished PC and mobile device hardware Setting up workstations Manage MS TEAMS ... - Mar 13
... Worked closely with the Quality and Regulatory team, during the FDA audit. Monitored and maintained Help Desk tickets in the Remedy system. Imaged and deployed refurbished PC and mobile device hardware Setting up workstations Manage MS TEAMS ... - Mar 13
Front End Field Engineering
Sunnyvale, CA
... Audio, video, digital conferencing, networks field system engineering Automotive safety and reliability standards, ISO 26262, FDA, IEC 61508 Creative thinking, agile and lean mindset, elegant works, fast learner, efficient communication and teamwork ... - Mar 10
... Audio, video, digital conferencing, networks field system engineering Automotive safety and reliability standards, ISO 26262, FDA, IEC 61508 Creative thinking, agile and lean mindset, elegant works, fast learner, efficient communication and teamwork ... - Mar 10
Scrum Master Program Manager
Redwood City, CA
... Managed developers around the globe to design, develop and deliver new software platforms following FDA guidelines. Led re-branding of department. Developed roadmaps and coordinated development activities for multiple GxP systems, (Quality Assurance ... - Mar 07
... Managed developers around the globe to design, develop and deliver new software platforms following FDA guidelines. Led re-branding of department. Developed roadmaps and coordinated development activities for multiple GxP systems, (Quality Assurance ... - Mar 07
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
Clinical Pharmacology Research
Morgan Hill, CA
... Reviewed FDA, EMA/CPMP, PMDA pre submissions and answered queries from referees for resubmissions. Clinical/Medical Project Director - Recognized leader in full-cycle project management with keen ability to consistently improve project efficiency, ... - Feb 12
... Reviewed FDA, EMA/CPMP, PMDA pre submissions and answered queries from referees for resubmissions. Clinical/Medical Project Director - Recognized leader in full-cycle project management with keen ability to consistently improve project efficiency, ... - Feb 12
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