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Quality Engineer Chemical Engineering

Georgetown, KY
... Meyer Page 2 monograph, FDA and source specifications. Investigate root causes for defects in finished goods and consult with vendors on relevant technical issues. Conduct inspection of equipment at the beginning of each day to assure machinery is ... - Dec 10

Project Manager Clinical Research

Jacksonville, FL
... meetings with major sponsors discussing topics such as queries, data, & audits Led team meetings for each service which included trainings, compliance with FDA, GCP and QA regulations Planning, Management and execution of biosimilar programs. ... - Dec 10

Information Architect, Software Architect, Program Manager, AI/BI/CI

United States
... Industry Regulatory Compliancy • Consulting Competencies • Strategic Pricing • Solution Sales • Solution Implementation Methodology • FDA Information Systems Assurance • Diploma in Health Services Candidate Manager of Transformational/Translational ... - Dec 09

Quality Training

Hebron, IL
... Reported directly to Quality Manger Medplast Quality Control Specialist August 2016 to October 2016 Responsible for all ISO and FDA compliances throughout company Edited and re-wrote policies and procedures Responsible for all CAPAs RMAs and ... - Dec 09

Manager Customer Service

Los Angeles, CA
... Documentation Management Complies with Business Practices and Procedures Compliance with CBP and PGA Laws and Regulations, FDA, EPA Customs Records Management Communications with Government Agencies Assigned to Several Major Accounts John Davis ... - Dec 09

Ophthalmic Technician

Clark, NJ
... New York, NY 10/1998 to 09/2000 New York Presbyterian Hospital, New York, NY Ophthalmic Technician, Performs preliminary eye exams on patients in her private practice on Park Avenue and managed an FDA clinical trial for hyperopic in the hospital. ... - Dec 08

Quality Engineer

New Haven, CT
... I have developed the ability to handle multiple tasks simultaneously and ensure all aspects of quality and manufacturing procedures under FDA regulations, SOP’s & GMP’s are carried out professionally and effectively to produce a successful outcome. ... - Dec 07

Medical Device Clinical Research

Richmond Hill, ON, Canada
... Sought for strong ability to cross-function as a team member, leader, problem solver and relationship building with working knowledge of cGMP, ICH GCP, FDA, ISO 13485 and OSHA regulatory guidelines. Excellent communicator with in depth knowledge of ... - Dec 07

Sas Data

United States
... Knowledge in preparing Integrated Summaries of Efficacy (ISE) and Integrated Summaries of Safety (ISS) reports for FDA submission. Thorough Knowledge and experience of Microsoft Office tools like MS Access, MS word, MS PowerPoint, MS Excel. Good ... - Dec 07

Safety Manager

Jonesboro, GA, 30236
... THORNTON LABORATORIES, Tampa, FL September 1989 – July 1994 Senior Analytical Chemist Performed analytical chemistry of environmental and industrial matrixes by official standard methods including EPA SW-846, AOAC, ACS, FDA, FPCA, TAPPI and others ... - Dec 07
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