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San Francisco, CA
... infusion rate •Reduced bill of materials to 30% under budget through negotiations with vendors •Gained knowledge of the FDA’s role in regulating and approving medical devices (PMA, 510k) Additional Projects: •Constructed a basic microscope to a ...
- 2018 Mar 19
San Francisco, CA
NUPUR PRABHU ac3vfp@r.postjobfree.com 443-***-**** San Francisco CA SKILLS ● Experienced in FDA audits,CAPA, Quality Metrics, Root cause analysis, deviation handling, hazard analysis,Validation ● Hands-on experience: HPLC, UPLC, Polarimeter, GC, ...
- 2018 Jan 01
San Francisco, CA
... •Clinical Research - (CRA, CRC, Consultant) – FDA Compliance/Quality, Systems/cGMP, GLP, GCP EDUCATION: • Clinical Trials Design & Management, SFSU 2007 • City College of San Francisco - Course: cGMP, GLP, GCP Spring 2004 • Completion of coursework ...
- 2017 Oct 19
San Francisco, CA
... Well trained in Good Clinical Practice (GCP), Good Manufacture Practice (GMP), Regulatory Compliance and FDA Guidelines. Excellent communication, leadership and collaboration skills. SAS Mainframe and SAS Programming Project Management and ...
- 2017 Aug 14
Santa Rosa, CA
... Commissioning Agents – Genentech Site, Vacaville, Ca 04/2009 - 08/2010 Process Equipment Commissioning Engr Interpret performance specifications for FDA & product/compound compliance. Process equipment validation testing, conformance & documentation ...
- 2017 Aug 06
San Francisco, CA, 94143
... Knowledge of US FDA regulation on drug development and health policy. 9. Computer skills: Microsoft Office, Corel Draw, Image J processing, Origin, ChemDraw, Igor and MDI-Jade. SELECTIVE RESEARCH PROJECTS: Postdoctoral researcher at University of ...
- 2017 May 24
San Francisco, CA
... Enhanced the mailing list generation system to improve performance Frank Fang – PL/SQL Developer Page 3 Enhanced the reporting module of FDA Approval Application, designed and developed a Windows auto release application for FDA Approval Application ...
- 2017 Mar 07
Richmond, CA
... Coordinate projects that are FDA regulated for software upgrades and software fixes. Using VPN for remote access, conducted customer hardware/software configuration on networking servers for hardware specifications. Created SOWs (Statement of Work), ...
- 2017 Mar 03
Santa Rosa, CA
... by the right personnel • Represented Manufacturing/Quality in presenting appropriate documentation/information during TUV and FDA audits following Current Good Manufacturing Practice standards • Develop testing protocol for PCBA Boards using company ...
- 2017 Feb 22
San Francisco, CA
... - Visualize results using R and/or Excel Present study findings to FDA clients, interpret study results and discuss future research directions Train junior analysts through performing code reviews, teaching SAS techniques and editing deliverables. ...
- 2017 Jan 12