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Resumes 61 - 70 of 203 |
Vista, CA
SUMMARY OF QUALIFICATIONS Medical devices, R&D, PLCs RF, AC/DC motor drives Manufacturing, sustaining FDA, IEC, ISO, GMP, JCAHO, FEMA Electromechanical drawing, design Verification/validation, IQ/PQ/OQ Written/verbal skills, meet deadlines Hands-on ...
- 2017 Sep 16
San Marcos, CA
... Performing duties in compliance with applicable FDA and state regulations as well as standards including, but not limited to, ISO 13485. Document internal audits and other quality assurance activities. Approval status updating the Engineering Change ...
- 2017 Aug 26
Vista, CA
... workforce while improving organization performance during the CTI (Clinical Transformation Initiative) according to FDA regulations Elicited and wrote software requirements and specifications for Rx and Dx medical devices and tracked changes ...
- 2017 Jul 14
Carlsbad, CA, 92009
... Select and order parts with EMI radiation and FDA safety regulation consideration. Build and document cables and assemblies for production. Collateral duties include: Maintain hazard materials log (MSDS), perform PMS, and maintain calibration on in ...
- 2017 Jul 11
Temecula, CA
... DMAIC, DFMEA, PFMEA, Value Stream Mapping (VSM), Design of Experiments (DOE), MSA (Gauge R&R), SPC, PCA, 8D, Work Instructions, FDA, CAPA • SAS-JMP, PLC programming, SolidWorks, Auto CAD, MS Access & Visio, SQL, VBA, MS Office • ERP Implementation, ...
- 2017 Jul 09
Carlsbad, CA
... 12/07) Senior Project Manager/ PMO Group Ballantyne - Global Recruiters Facilitated Program management of several related projects and enhancements, utilize ECM/ DCM Documentum, Oracle and Regulatory Intelligence on new FDA regulation initiatives. ...
- 2017 Jun 28
Temecula, CA
... Supervised a five-person crew to develop and validate the Xience V particulate test when FDA rejected the filing data for particulates. The first particulate validation report written by our team was accepted by the FDA, which expedite Xience-V ...
- 2017 Apr 11
Oceanside, CA
... pricing, brand management, market strategy Continuous improvement / lean manufacturing lead Regulatory and compliance (FDA, EPA, OSHA), medical drugs and devices Budgeting (capital, business and operations) cost control while supporting growth ...
- 2017 Mar 09
Vista, CA
... SAP, E2, Bill of Material (BOM), Microsoft Office, Microsoft Project, EPDM • Process ISO 9001, ISO 14001, ISO13485, FDA Regulation, Lean Manufacturing, 6S Kazien • Standards: GD&T/ASME Y14.5, UL, Panasonic Safety Standards, NFPA, OSHA, Six ...
- 2017 Mar 02
Carlsbad, CA
... Working knowledge of the FDA Quality System Regulation and the Medical Device Directive. Project documentation and validation. ATA Real State & Construction, Los Angeles, USA Jun 2005- Jan 2006 Software Developer/System Analyst Web site analysis and ...
- 2017 Feb 17