|
Resume alert |
Resumes 91 - 100 of 179 |
Tampa, FL
... Responsible for conducting and/or participating in regulatory Audits by FDA, MHRA, Turkish Authority, ANVISA, Corporate and customer cGMP Audits, as well as, PAI Regulatory Inspections. Effective communicator and mentor. Customer and results ...
- 2017 Jul 30
Tampa, FL
... Review files and documents prior to distribution to FDA Inspectors; Developed and maintained complex project files pertaining to raw material batch records; prepared travel arrangements and agendas; coordinated staff & unit head meetings; prepared ...
- 2017 Jul 08
Clearwater, FL
... Producing detailed drawings necessary to fabricate fixturing and components as per FDA, ISO and B&L. COBHAM (Conax Florida Corp), Saint Petersburg, Florida 2008 – 2012 Conax, an Aerospace and Defense product supplier; have been producing leading ...
- 2017 Jun 21
Saint Petersburg, FL
... •Solely and successfully moved the client request center from the client location to an HP facility, after it was initially thought it would not work, due FDA Regulations and initial lack of security. Netting a reduced operations cost. Personnel ...
- 2017 May 20
Saint Petersburg, FL
... I am very familiar with all DEA, GMP and FDA regulations. I have been awarded many special recognition letters and awards from upper management for my innovations to improve production. WORK EXPERIENCE Catalent Pharma Solutions, St Petersburg, ...
- 2017 May 04
Largo, FL
... settingsSign out Production job in Largo, FL - April 2017 Posted date: Apr 21 cstconnection jobs Summary: press, fda, gmp, packing, packaging, machines, mechanical, electrical, material, manufacturing Your Email: acz0cl@r.postjobfree.com ...
- 2017 Apr 27
Tampa, FL
... 08/07 to 01/08 IBM, RTP, North Carolina (Consultant through CDI) Lead Java Developer Responsible for Java programming and debugging SCORE web application, a workflow approval processing software for the FDA, using Java, Rational Application ...
- 2017 Apr 25
Clearwater, FL, 33763
... Qualifications Summary Industry experience: Medical Device, Aerospace (Space Shuttle), Military, Manufacturing Functional leadership and management accountabilities: •Worked on FDA QSR (21CFR 820/210/211) & ISO 13485 Quality. •Key interface for, DOD ...
- 2017 Apr 12
Tampa, FL
... Analytical~ Negotiation ~ Critical Thinking~ Communication & presentation skills ~ Documentation OTHER SKILLS SDLC, ITIL, SOX, FISMA, PCI, ISO, HIPAA, FDA, EU, CDISC, Scrum, Six Sigma. AWARDS Awarded 7 times for innovative ideas and stellar job.
- 2017 Mar 30
Clearwater, FL
... Aided in FDA remediation. Lead Root Cause Analysis, initiated and lead product improvement project to eliminate the number one cause of customer complaints with negative pressure device. Process Engineer, 2007-2013 Led and supported multiple ...
- 2017 Feb 02