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Resumes 81 - 90 of 240 |
Longmont, CO
... Core Competencies & Strengths: ISO 9000, QMP Solidworks, Matlab, Simulink FEA, ANSYS Solar / Electro-Mechanical Design Process Redesign & Improvement ASME XI, NFPA, and FDA experience LEAN, FMEA, Six Sigma, QA/QC Test Documentation PROFESSIONAL ...
- 2017 Jul 12
Louisville, CO
... with all applicable procedures, (Standard Operating Procedures) SOPs, cGMPs, company policies, health and safety requirements, procedures and corporate policies and any other quality or regulatory requirements (For example: FDA,NDLEA etc.). ...
- 2017 Jul 06
Denver, CO
... Advised the QA department on the clinical implications of all customer incidents and participated in responses to the customer and/or FDA and helped prepare HHE's for submission to FDA • Adjunct Professor for Pharmacy Law and Sterile Compounding and ...
- 2017 Jun 10
Littleton, CO
... Each design was created on an individual basis to patient’s unique anatomy according to FDA, EMA and ISO approved quality standards and built using SLA printers. Colorado School of Mines – Golden, CO 09/2015 – 05/2016 Engineer Worked as part of a ...
- 2017 May 31
Denver, CO
... Additional experiences: 4 years with commercial lending and banking software, 1 year writing marketing content for an FDA-regulated nutritional supplement, and 1 year documenting a remote medical epidemiology device and applications, SOPs, SOWs, and ...
- 2017 May 30
Denver, CO
... Post ASD Closure with Amplatzer and Helex Septal Occluder Devices A review of the literature to compare the presence of residual shunting following ASD closure with each of the two FDA-approved septal occluder devices, the Amplatzer and Helex. ...
- 2017 May 30
Denver, CO
... In-depth knowledge of FDA and HIPAA compliances Clinical Trials Excellent communication skills (verbal and oral) including platform-speaking skills Excellent prioritization and organizational skills 5 Analyzing financial information and proficiency ...
- 2017 May 03
Broomfield, CO, 80020
... Experience CAD Designer – Zimmer Biomet Spine (Contractor) – Broomfield, CO July 2016 – Present ●Updated engineering drawings of orthopedic implants and instrumentation to comply with FDA regulations. ●Gained strong experience in both modeling and ...
- 2017 Apr 11
Denver, CO
... Maintained Design History Record and Design Master Record documentation to be compliant with FDA regulations. - Testing: Tested DV, Biocompatibility, Sterilization, Validations, and DOE devices and materials. Testing consisted of tensile, ...
- 2017 Mar 28
Black Hawk, CO
... Manufacturing Concepts and Implementation Discrete / Repetitive Manufacturing CAPA resolution and Quality improvements Project Presentations Production Flows for GMP Protocols and FDA documentation Professional Experience Senior R & D Engineer Nov. ...
- 2017 Mar 14