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Fishers, IN
... *FDA Medical Device Manufacturing environment. *Scheduling shift production.*Good Manufacturing Practices(GMP). *Good Documentation Practices(GDP).*Standard Operating Procedures(SOP). *AS-400.*Forklift certified. *Monitoring employee attendance (ADP ...
- 2016 Dec 15
Fishers, IN
... from around the globe -Enforce contracts that have been signed previously with a company that was bought by Eli Lilly -Prepare for FDA and other global agency inspections in keeping with the inspection readiness protocols -Define Lilly business ...
- 2016 Oct 14
Indianapolis, IN, 46237
... Wrote reports per FDA regulations. Education BA English, Butler University (2006) Active Certifications and Affiliations Licensed Esthetician, Empire Beauty (2010) PMP, Project Management Institute (2015) Training Managing Multiple Projects, IUPUI ...
- 2016 Aug 19
Indianapolis, IN
... ISO 13485 and FDA Regulated Office Administrator/Benefits Administrator 9/2008-2/2009 My Health Care Manager, LLC Coordinated all HR functions with PEO – Professional Staff Management. Established office systems and procedures to streamline office ...
- 2016 Aug 10
Indianapolis, IN
... Familiar with FDA Good Manufacturing Practices (GMPs), Good Laboratory Practices (GLPs), and Good Clinical Practices (GCPs) regulations, Part 11 Electronic Records, Electronic Signatures requirements, ICH guidelines. Extensive experience with ...
- 2016 Apr 28
Indianapolis, IN
... I have also been present and directly answered questions for internal and external client audits, including an FDA inspection. I have been able to prove and stand behind Covance standards through documentation as I was also a Quality Assurance ...
- 2016 Apr 12
Indianapolis, IN
... of hearing loss 31 TIA safety information 35 Safety information 37 FDA Consumer Update 40 Nine Driver Safety Tips 44 Consumer Information on SAR46 STANDARD LIMITED WARRANTY50 2 A Message from Coolpad Thank you for purchasing your ROGUE mobile phone! ...
- 2016 Apr 03
Indianapolis, IN
... Regulatory Environments: FDA, DCMA, NRC (materials), FAA, FCC, and Insurance. SW / Systems / Business Requirements: evaluate, elicit, and engineer with / without use cases Storyboard in Use Cases Traceability of requirements, design, test artifacts ...
- 2016 Mar 01
Carmel, IN
... FDA Audits Education: BS, Educational Technology, Indiana State University Career History Warehouse/Distribution Center Manager, Grote Industries, April 2015 to December 2015 Supervise the receiving, shipping and picking operation of midsize ...
- 2016 Feb 22
Indianapolis, IN
... , Indianapolis, IN Sep 2003 - Sep 2004 Contract Senior Project Manager Engagement at Roche Diagnostics Corporation responsible for managing several simultaneous quality control, FDA Part 11, validation, and manufacturing custom software projects. ...
- 2015 Dec 16