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Greenville, SC
CAMERON SCOTT SCHNABEL *** * ****** ****** *** **02, Greenville, SC 29601 610-***-**** • adfl5o@r.postjobfree.com Biomedical Engineer TECHNICAL SKILLS SolidWorks (Certified) Design Research and Development Prototyping Patent Searching FDA Regulatory ...
- 2020 Aug 26
Greenville, SC
... Directed efforts to be compliant with FDA regulations regarding employee competency & training, recordkeeping & training effectiveness. Implemented Pay for Performance (PP) plan for Liquid and Nicogen manufacturing operations. BRM, Corporation ...
- 2020 Aug 02
Greenville, SC
... Spearheaded FDA 510K Submission and 510K Exemption for non-wireless version of medical device. Member of management team that sold company in March 2019 Trans-Radial Solutions (2014-2016) Sales Director/Legal Consultant Dealt directly with lead ...
- 2019 Dec 14
Taylors, SC
... * Real time PCR detection of HPV 16.18.31.6,11 particles from Lavage samples * Completed 12000 patients samples study from worldwide for safety, efficacy study * Ensure all clinical sample test records and documents completion for FDA inspection * ...
- 2019 Nov 16
Simpsonville, SC, 29680
... Departmental budgeting The Blood Connection ● Piedmont, SC ● January 2008-Aug 2013 Blood Collection and Pharmaceutical Manufacturing Manager, Quality Operations External Inspection Coordination/Hostess (FDA/CBER, AABB, DHEC). Personnel selection and ...
- 2019 Jul 25
Simpsonville, SC
... of all new product, • updating quality documents, SPC, • deviant material and disposition of inventory, • regular FDA inspections, and maintaining GMP Education College courses in Business Management Ethic courses, Calibration, Kizan, PPAP ...
- 2019 Jul 22
Mauldin, SC
... for business improvement and process analysis, primary contact for task groups and launch of quality measures & training, FDA Approval Submittals Six Sigma, Stephen Covey Training Change Management: Creation and implementation of change control ...
- 2018 Nov 08
Greenville, SC
... Equipment and Process Validation, Problem Solving/RCA based on PDCA and DMAIC methodology, Experienced in FDA, TüV and LRQA Audits, Ergonomic and Safety assessment, Continuous Improvement, Lay Out, Workstations and Production Systems design. ...
- 2018 Jan 19
Easley, SC
... Supplier Quality Engineer for High Voltage Capacitor Manufacturing Value Streams •Simplified & Implemented Quality Policies to better comply with QSR, FDA & ISO regulations •Process Validation, Equipment Verification, Facilities Systems Validation, ...
- 2018 Jan 14
Fountain Inn, SC
... B Regulations trained auditor Lotus 1-2-3 LIMS Minitab MS Word Suites FDA/AIG AIAG, Standards training Trainer/ Facilitator for Continuous Improvement projects Quality Alert’s/8D’s Reporting Warranty Reporting Certified Star Leader and Human Factors ...
- 2017 Jun 19