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Resume alert |
Resumes 21 - 30 of 575 |
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
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
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
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
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
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
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
San Jose, CA
... (GMP/ISO/FDA/USDA/REACH/RoHS/EU compliant) o Quality Management, Audit, Compliance, Qualification standards and implementation o Maintenance process and implementation standards of excellence (PM, Upgrade, Installation, Logistics). o Contract ...
- Jan 19
Menlo Park, CA, 94025
... 60950, as well as FDA regulations (21CFR820), ISO 13485, and the 510(K) clearance process. Skilled in managing projects, with excellent communication and interpersonal abilities. Highly self-motivated and dedicated to ensuring the safety and ...
- Jan 18
Cupertino, CA
... Designed and automated the MAUDE process for RPMS team which performs monthly review of device related complaints from FDA and tracks it in SQL database. Created a master data for all complaints related to Intuitive’s products and managed this data ...
- Jan 18