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Medical Technologist Data Entry

Zebulon, NC
... Review literature articles and process adverse event reports from literature per project and FDA guidelines. Maintain knowledge and understanding of PPD and client-provided SOPs and current FD regulations. Effectively communicate with project team ... - Jul 16

Medical Device Design

Edison, NJ
... Medical device Regulations: FDA 21CFR 820, ISO Standards EXPERIENCE Graduate Student- Cai Lab, Rutgers University Feb 2017 - Present Secondary Data analysis for Single Cell RNA sequencing. Identification of novel aberrant genes in heterogeneous mass ... - Jul 16

Engineer Manager

Highland Mills, NY
... Quality Assurance overseeing all FDA and ISO 13485 (Medical Device) compliance. Perform instrument calibration per ISO/ANSI/NIST or any government regulation requirements. Write all Standard Operation Procedure (SOP) used for Instrument Calibration, ... - Jul 16

Contract administrator

Alexandria, VA
... Monitored and reviewed department documents to insure DOT and FDA regulations were in compliance. Reviewed weekly work schedules of all departments to ensure their logistics needs were being met. Designed, reviewed and monitored vehicle maintenance ... - Jul 16

Manager Engineer

Minneapolis, MN
... Fully familiar with OSHA, EPA, FDA, ISO and related industry and government regulations. Recognized as keynote conference speaker and subject matter expert. Strong professional performance in general management, site inspections, root cause analysis ... - Jul 15

Supply Chain Manager

Menlo Park, CA
... Trend monthly activities, training completion, inventory/reconciliation exceptions, annual reconciliations, signature audit outcomes & FDA reporting across each sample program lifecycle. Monitored process health indicators to drive improvements ... - Jul 15

Quality Engineer Continuous Improvement

Scottsdale, AZ
... FDA GMP Médical Devise 21 CFR 820 Certification FDA GMP Pharmaceutical 21 CFR 210 - 211 Certification FDA HACCP Training FDA GLP 21 CFR 58 Certification 510K and 483 experience Supplier Development Programs/Launch for new product and APQP programs ... - Jul 15

Assistant Dental

Pleasant Grove, UT
... Prepped machines and food to comply with FDA regulations.. Maintained a clean and sanitary work environment. ᅳ Education Mountainland Technical College Certified Dental Assistant, Completion Currently attending school in order to graduate with a ... - Jul 14

Highly Experienced Project Manager with PMP since 2001

Austin, TX
... Led business separation testing for LMS system with interfaces to FDA regulated manufacturing Quality Systems. Project Manager separating global integrated PeopleSoft HR system between two rival companies. Separated Human Resources, Payroll, ... - Jul 14

Sales Representative Assistant

Los Angeles, CA
... Utilized GMP/GLP guidelines, evaluated and confirmed package insert claims for FDA approval Used CLIA guidelines and in-house protocols for testing Prepared reagents and maintained instruments Trained lab personnel Performed colorimetric bead/ ... - Jul 14
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