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Resume alert |
Resumes 91 - 100 of 216 |
Charlotte, NC
... * Performed technical and GMP gap assessment of quality system against ISO 13485 standards and FDA 21 CFR Part 820 requirements and developed/ revised/ enhanced procedures in preparation for pending ISO audit and planned product transfer to a ...
- 2017 Dec 13
Rock Hill, SC
... and seminars Serve as a liaison between DHEC and the community Responsible for reading and re-reading Regulations 61-25 and FDA Food Code Taken at least 20 FDA ORA-U online classes (Required 5-10 per year) Winn Dixie Rock Hill, SC Customer Service ...
- 2017 Oct 08
Charlotte, NC
... FDA Responses-Complete response letters, problems encountered during drug manufacture, safety, efficacy, bioequivalence, stability, quality of final product, labeling. Research experience Duke University medical research scientist, carrying out ...
- 2017 Oct 05
Gastonia, NC
... Dispense and removal of hazardous materials per safety and FDA protocols. Certified and trained 12 new employees at 5 stations for the new production line in Ireland. Superior Automotive, Morgan Hill, Ca 2011-2013 Office Manager and Bookkeeper. ...
- 2017 Aug 21
Charlotte, NC
... Controls, Risk Management, CAPA, Post-market Surveillance, Writing Validation Protocols- IQ/OQ/PQ/ SOP’s, Process Validation, Master Validation Plans, Pro-E, Remediation, PFMEA, 21 CFR Part 820 - Quality System Regulation (QSR), FDA and Gage R&R. ...
- 2017 Aug 14
Charlotte, NC
... and customers Recall Administrator, leading customer communication and collection of required documentation in collaboration with FDA requirements Microstrategy Super User, managing the integrity and reporting of data for Fresh Express Operations, ...
- 2017 Aug 08
Charlotte, NC
... Documented according to FDA standards. Manufactured device using circuitry analysis and Solidworks. Portable syringe pump, May 2016 – June 2016 Designed a portable insulin syringe pump using Solidworks and produced a functional syringe pump with a ...
- 2017 Aug 05
Charlotte, NC, 28269
... Tracking documents assist QA with preparation readiness ensuring we are in compliance for FDA visit. Travel arrangements, Concur expense reporting, schedule conference-call, conference rooms. Self-starter who meets project deadlines and requirements ...
- 2017 Mar 11
Charlotte, NC
... Application allowed FDA quick, flexible access when evaluating drug. 1988-1989 Allied Signal Assisted various groups in SQL specification and optimization; SQL*Forms instruction; taught SQL course to various divisions. Fortex Corporation 1986-1987 ...
- 2017 Feb 16
Charlotte, NC
... • Perform failure analysis on stress and strain testing of mechanism under simulation, which were cross-referenced with mathematical calculations • Established FDA 510k premarket allocation for class 2 medical device along with research of ISO ...
- 2017 Jan 23