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Resumes 11 - 20 of 662 |
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
Hayward, CA
... Department of Ag) SSOP (Standard Sanitation Operating Procedures) HACCP (Hazardous Analysis Critical Control Points) FDA (Food & Drug Administration) GMP (Good Manufacturing Practices) all safety policies and procedures and any other established ...
- Mar 16
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
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
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
San Bruno, CA, 94066
... South San Francisco, CA Labeling and Compliance Assistant in Regulatory Affairs, dealing directly with the FDA, JAMA, and the New England Medical Journal; and assisted with the Product Review Committee. Patent Litigation for the Legal Department: ...
- Mar 02
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
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
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
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