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Resumes 51 - 60 of 216 |
Rancho Trabuco, CA, 92688
... Irvine, California 2012 to Present Product Design and Development Engineer • Design and prototype sheet metal and plastic enclosures for medical imaging devices, image collectors/scaler and recorders under ISO 13845 and FDA standards. • New Product ...
- 2021 Mar 18
Riverside, CA
... Maintained company's compliance of FDA, USDA and SQF Quality Control Technician Sep – Dec 2012 HALIBURTON INTERNATIONAL FOOD. Ontario. Daily quality inspection of fresh, dried, pre-processed, IQF vegetables, and food ingredients. Executing daily ...
- 2021 Mar 02
Laguna Niguel, CA
... Analysis of test results and planning data driven strategies for optimization and development purposes Assisting in Patenting and FDA submissions (510K & Letter to File) Post-Doctoral Research Associate – Louisiana Tech University (Ruston, LA) Pool ...
- 2020 Nov 04
Riverside, CA
... containing an NFC reader to interface with product (blister pack) •Researched and developed an optimal business plan as well as implemented FDA medical device standards and cGMP regulations in the manufacturing plans and take-to-market strategies. ...
- 2020 Oct 08
Moreno Valley, CA
... Over 25 years working with medical devices in compliance with GMP, ISO 13485, 21 CFR Part 11 & Part 820, ISO 9000, and similar standards for FDA Compliance. Bilingual (English and Spanish). SPC Certificate SolidWorks Excel Word Power point Microsoft ...
- 2020 Jul 04
Mission Viejo, CA
... Worked in regulated industries: Automotive (AEC-Q100), Medical (ISO 13485 and FDA regulations). Experienced user of Altium, Matlab, C, C++, C#, ANSYS FEA, COMSOL FEA, EMPIRE FDTD, Python, Autocad, Solid Works, LabView, Orcad, Agile. SELECTED ...
- 2020 Jul 02
Mission Viejo, CA
... for Applied Medical, a medical device company under Technical Development and Engineering department, responsible in ensuring the Quality of the medical device product in a regulated industry: FDA Regulations and other Quality System Regulations. ...
- 2020 Jun 03
Mission Viejo, CA
... Significant pharmaceutical/medical device company experience including Quality management standards including general manufacturing practices, FDA Quality System Regulation, and ISO Standards performing accounting, payroll, and human resources. ...
- 2020 Jun 01
Murrieta, CA
... Strong understanding of FDA medical device requirements and Quality system standards. Exceptional communication and interpersonal talents backed by ability to concisely convey highly technical concepts to a wide variety of skill levels WORK ...
- 2020 Mar 28
Mission Viejo, CA
... solutions, following FDA procedures and protocol. Provided analysis of I.V. solutions and plastic containers. Prepared and released pilot plant I.V. solutions to plant filling line. Swedcast Corporation, Florence, Kentucky and Swedlow, Inc., Garden ...
- 2020 Mar 25