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Online Resumes with "Cfr Title"
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Research
To obtain a challenging position within the Pharmaceutical industry or medical devices industry that will allow me to use my experience to play a key role in Clinical Research studies and projects, and/or product development with medical devices.
Tags for this Online Resume:
Clinical Pathology, laboratory method development, IQ, OQ, PQ, instrumentation, validation of medical devices, Regulatory, GLP, GCP, IRB, TMF, Project Manager, Documentation Specialist, Scientist, Archives
Technical Writer / Tech Pubs Manager -- 15 years Experience -- SF Bay Area
Summary of Qualifications Manager and technical writer with more than 15 years experience in technical writing and editing originally in the field of training and instructional design, but recently in the financial, hi-tech, and utility industries creating standards, procedures, and other business documents. * BS, MBA, Certified Technical Writer * Familiar with Federal Regulations: CFR Title 49 (FRA), CFR Title 14 (FAA), CF...
Tags for this Online Resume:
Management, Documentation, Spreadsheet, Utilities, Publications, Training, Technical Writing, Transportation
Not Listed - 20 Years of Experience - Near 33010
Experience Summary: College Professor, Miami Dade College. Miami, Florida. Aviation Accident Investigator: United States, National Transportation Safety Board domestic and foreign investigations. Aviation: aircraft maintenance, safety, and manager. Mechanic to supervisor. United States Air Force military and civilian (Code of Federal Regulation {CFR}, Title 14, Part 91, 121, 129, 135, and 145) maintenance and aviation safet...
Tags for this Online Resume:
Power Plants, Management, Project Management, Project Manager, Airlines, Logistics, Procurement, Utilities, Engineering, Corrective Actions
Biological Technician - 3 Years of Experience - Near 94303
Summary: Experienced commissioning engineer with over 12 years of practical experience in biotech. Proficient with most equipment related to cell culture fermentation, and oral solid dose pharmaceutical manufacturing facilities. Very strong in GMP documentation FDA, ISO 9000, cGMP, CFR title 21 and DEA regulatory compliance. Familiar with LIMS, BMS, Trackwise, Faciliworks, Word, and Excel.
Tags for this Online Resume:
Documentation, Automation, Honeywell, Schematics, Pharmaceutical, Science, BMS, Compliance, Good Manufacturing Practices, ISO, Validation
Quality Control
SUMMARY OF QUALIFICATIONS Quality Systems - Quality Control /Quality Assurance Management of Analytical Laboratories/Quality Audits/Scientific Technical Services Liaison Highly motivated, key contributor in Quality Management and cGMP compliance with more than twenty five years of demonstrated growth and success in scientific applications with Contract Manufacturing Organizations in Quality, R&D and manufacturing. Recognize...
Tags for this Online Resume:
Analytical Chemistry, Chemistry, Manufacturing, Research and Development, Commercial Production, Compliance, Packaging, Pharmaceutical, Documentation, Quality, validation, Audits
Research
To obtain a challenging position within the Pharmaceutical industry or medical devices industry that will allow me to use my experience to play a key role in Clinical Research studies and projects, and/or product development with medical devices.
Tags for this Online Resume: Clinical Pathology, laboratory method development, IQ, OQ, PQ, instrumentation, validation of medical devices, Regulatory, GLP, GCP, IRB, TMF, Project Manager, Documentation Specialist, Scientist, Archives
