| Resume alert | Resumes 81 - 90 of 209 |
Sales Software Developer
Charlotte, NC
... development, maintenance, and support of JD Edwards applications for manufacturing, distribution, inventory, and sales order modules for Greer Labs via a strict protocol upon verification of scripted testing and in accordance with FDA regulations. ... - 2018 Jul 25
... development, maintenance, and support of JD Edwards applications for manufacturing, distribution, inventory, and sales order modules for Greer Labs via a strict protocol upon verification of scripted testing and in accordance with FDA regulations. ... - 2018 Jul 25
Engineering Design
Mooresville, NC
... Design requirements covered the ASTM and FDA SOPs that would be followed, the general regulatory standards for an external aesthetic restoration prosthesis, and a class 1 device, the scope, general marketing information, user needs, engineering ... - 2018 Jun 20
... Design requirements covered the ASTM and FDA SOPs that would be followed, the general regulatory standards for an external aesthetic restoration prosthesis, and a class 1 device, the scope, general marketing information, user needs, engineering ... - 2018 Jun 20
Management Sales
Charlotte, NC
... Worked with the Quality Assurance group to ensure all systems, including Spectrographic, Chromatographic and Dissolution apparatus were within FDA compliance. Installed, validated, calibrated and operated two Zymark Tablet Processing Workstations ... - 2018 Jun 06
... Worked with the Quality Assurance group to ensure all systems, including Spectrographic, Chromatographic and Dissolution apparatus were within FDA compliance. Installed, validated, calibrated and operated two Zymark Tablet Processing Workstations ... - 2018 Jun 06
Manager Quality
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
... * 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
Environmental Health Safety and Compliance
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
... 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
Medical Assistant
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
... 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
Customer Service Engineering
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
... 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
Engineer Professional Experience
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
... 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
Sales Supply Chain S&OP Demand Planning
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
... 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
Manager Assistant
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
... 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