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Clinical Research Manager

San Jose, CA
... Monitored clinical trial, ensuring subject safety, essential document collection, data and procedure review, and compliance with study protocol, FDA and HIPAA regulations, and ICH / GCP Guidelines. NAVAL MEDICAL CENTER, SAN DIEGO, San Diego, CA 2010 ... - Apr 23

Administrative Assistant Medical

Hemet, CA
... Auditor Purchasing MIDAS Quality Measures HEDIS (Healthcare Effectiveness Data and Information Set) Data Mining LEAN Trained FDA Knowledge PeopleSoft Epic (EMR) Press Ganey Education June 2010 Everest College - San Bernardino, CA Certification in ... - Apr 22

Document Control Manager

Hayward, CA, 94544
... MS Office Suite, Visio, QSR, GMP Quality Assurance/Control Standard Operating Procedures Strategic Planning & Analysis Training & Development MasterControl, Adobe Acrobat, Epicor FDA 21 CFR Part 820/Part 11 Professional Experience ALLERGAN INC. ... - Apr 22

Management Manager

Richmond, VA
... Ensured compliance with FDA, OSHA regulations for federal and state guidelines. Reviewed progress reports with staff and expedited corrective measures where needed. Procured raw materials and examined the quality of all finished and raw products. ... - Apr 21

Machine Operator Foreman

United States
... •Assure all GMP, ISO, FDA, and OSHA Policies and Procedures are met by self and supervised employees. •Maintain open dialogue with Maintenance Department to assure all routine, non-routine, and preventative maintenance is performed at ideal times to ... - Apr 20

Customer Service Sales

Kennesaw, GA
... gathering parts,, tools, and materials Responsible for assembling and packaging various Philips Respironics medical devices and subassemblies in an ISO 9001 and FDA regulated environment. Working knowledge of Demand Flow Technology (DFT) system to ... - Apr 20

Technical Operations Management and Program Systems Engineering

Marietta, PA, 17547
... Regulated environment compliance experience with FDA Medical Device, EPA Small Engine, and ITAR Programs Management Skills: Operations and Facility Development, Program Management, Risk Management, Requirements Management, Stage Gate PDP, Resource ... - Apr 20

Microsoft Office Raw Materials

Dover, NJ
... Reject all that does not pass my qualification Supplier complaints Customer complaints Label printing and working with USDA and FDA on label creation SOP maintenance and creation Experience with SQF, HAACP Personal Assistant (Sept 2016-Jan 2017) ... - Apr 20

Project Management

Mauldin, SC
... Supplementary Preliminary Engineering Assessment and Project Execution Plan, Root Cause Analysis, Risk Analysis, Summary Reports, Technical Offers, Functional Specifications, Technical Specifications, Client Summaries, FDA Approval Submittals; ... - Apr 20

validation engineer equipment validation

San Francisco, CA
... Thorough knowledge about pharmaceutical/medical device regulations like FDA 21 CFR Part 11, part 820 and on ISO 13485/Part 820 / ISO 14971 Expertise in various SDLC methodologies such as Agile, Scrum and Waterfall in creating various protocols for ... - Apr 20
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