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Resumes 81 - 90 of 216 |
Mooresville, NC
... Delivered governmental compliance updates to the GuidingStars.com site for FDA mandated nutrition changes saving 1000’s in potential fines. Lead all efforts for the re-platform and rewrite of the internal GuidingStars.com program on the Azure Cloud. ...
- 2019 Jun 17
Charlotte, NC
... o Strict adherence to regulated environment like FDA guidelines and follow pharmaceutical industry wide best practices. Winning Contributions for project – Credit Insurance System for Pricing – CUNA Mutua Group, Madison WI: oProject Lead / Manager ...
- 2019 Mar 22
Charlotte, NC
... Environment) DMS Client : Baxter, Bangalore, India Employer : Wipro Technologies, Bangalore, India Duration : Jun 2013 – Jan 2014 Description: BaxEDGE is a new solution for managing global content for electronic/paper submission to FDA, EMEA etc... ...
- 2019 Jan 03
Fort Mill, SC, 29708
... Working knowledge and practical experience with cGMP, GDP, GLP and FDA regulations in a chemistry laboratory environment. Familiar with quality systems [i.e. Laboratory Investigation Reports (LIR), Corrective and Preventive Actions (CAPA), ...
- 2018 Dec 05
Charlotte, NC
... CAREER EXPERIENCE ClinLab Staffing Agency Contract FDA Quality Control Analyst Client: Greiner Bio-One - medical device mftg. Jan 2018- July 2018 Quality Control Analyst for medical device manufacturer, monitoring all FDA audit compliances. ...
- 2018 Nov 27
Charlotte, NC
... US FDA audit was successfully completed twice without any observation from the inspection and packing department. Similarly, TGA audit was also concluded without any observations at Mylan Laboratories Limited. Successful implementation of ...
- 2018 Nov 19
Charlotte, NC
... CMMI course certificate FDA Quality Assurance Seminars and certifications AAMI Verification and Validation Seminars and certifications Quality Assurance Institute – C.S.T.E. Certified Software Test Engineer Continua Health Alliance (medical device ...
- 2018 Sep 21
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
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
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