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Resumes 11 - 20 of 585 |
Fremont, CA
... •Familiarity with FDA QSR and ISO 13485 medical device regulations. •Strong Experience in Mobile Testing with brew, symbian,, Android winmo . •Knowledgeable in testing mobile applications on Brew Simulator, Emulator, Android ADB Log Cat and device ...
- Aug 23
San Jose, CA
... Develop surgery kits adhering to imperative FDA guidelines and within constraints of demanding time. Negotiate and support logistics costs meant for 3rd party logistics providers assisting yearly budget goals. Ensure to process orders and on-time ...
- Aug 19
Sunnyvale, CA
... Meter design was submitted as part of a 510(k) submission (FDA’s pre- market notification) in June 2011. • Previous battery contacts were difficult to assemble into the device, and were prone to yield after drop. Performed mechanical redesign of ...
- Aug 08
San Jose, CA
... ● Managed the certification program in compliance with FDA and USDA regulations, saving the company 30% in costs within a year by optimizing processes. Vendor Management Program (Del Monte Foods Inc.) Managed the ingredient approval and vendor ...
- Jul 23
Fremont, CA
... products (Lingo Mobile Health care App) validating and meeting compliance with regulatory and corporate requirements (Such FDA standards, 510K approval ) Review requirement and ensure Tested requirement met FDA standards & work directly with SWQA ...
- Jul 17
San Jose, CA
... Supported ISO 13485-2003, cGMP and QSR 21CFR820.50 and FDA audits ERP experience with Oracle and MS Dynamics Great Plains. Experience of start-up environment, low volume high mix as well as high volume production Deep understanding of manufacturing ...
- Jul 16
Fremont, CA, 94536
... Service Optimization Laboratory Management Lean-6 Sigma Manufacturing Continuous Improvement Regulatory Compliance FDA, ISO 9001, 13485 In-Vitro Diagnostic & Med Device Manufacturing Strategies EMD Electronics – Merck KGaA, Santa Clara, CA ...
- Jul 10
San Jose, CA
... Database Management Continuous Improvements Accountability & Efficiency Customer & Stakeholder Engagements Problem Resolution FDA & ISO Regulations Teamwork & Cooperation Product Quality & Deliverables E-Procurement Commodity Trends Global Supply ...
- Jul 09
San Jose, CA
... 1.Coordinating and scheduling software releases from internal engineering to production systems recording change execution to comply with SOX, FDA, CLIA (Clinical Laboratory Improvement Amendments) and other auditing requirements. 2.Proposing and ...
- Jun 29
Pleasanton, CA, 94566
... Knowledgeable in various import/export/VAT, project management, logistics, & regulatory disciplines related to logistics &shipping processes of medical devices related to FDA, GMP, SOP, ISO 9001 & ISO 13485. Seeking to leverage diverse experience to ...
- Jun 27