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Online Resumes with "SOP Writer"
Versatile and Innovative Quality Management professional skilled at seeing the “Big Picture” while still focusing on the details. Expertise in Streamlining Processes and Systems. Diligent and Motivated to improve processes and increase revenue. 20 year veteran with the same company with extensive background to share with a new Company
Compliance manager, compliance auditor and monitor, instructional designer, policy analyst, SOP writer, technical communicator, project manager, validation specialist, usability tester, and medical technologist. More than 15 years of practical knowledge and experience in biopharmaceutical industry, research and clinical laboratories, healthcare consulting, and pharmaceutical manufacturing.
Summary Accomplished QA Manager presently working in a quality-oriented environment within the Non-Profit arena. Formerly a Quality Engineer with the Department of Defense. A qualified individual with demonstrated experience and success in modern inspection techniques, project management, quality assurance sciences and quality control accompanied with hard work ethics and multitasking skills Focused and result driven profes...
Searching a position as senior/principal quality, manufacturing, R&D engineer focused in mitigation, remediation, redesign and process change for cost savings and product quality enhancement, CAPA initiation and execution, and new product development.
Ideal Companies: medical or Aerospace industries
Tags for this Online Resume: Manufacturing, Medical Devices, Product Development, Research and Development, R&D, IQ/OQ/PQ, Pfmea, Dfmea, Certified Quality Auditor, Six Sigma/ Lean Sigma Green Belt, Quality Foundation Deployment Green Belt, MiniTab, Managing Cross Functional Teams, Solid Works Design, Conceptual Design, New Product Development, Risk Analysis, Negotiations, Customer Relations, Value Engineering, Decrease Field Failure, Increase Customer Satisfaction, Report writing, Authoring and enhancing Standard Operating Procedure, ISO 13485, ISO 14971, ISO 60601-1, Authoring Quality Manual, Design Validation, Verification, Valves, Switches, Linkages and mechanism design and development, Complaint Handling