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Online Resumes with "NCMR"
Corporate or mid-size companies requiring an experimented Quality Profesional with very good knowledge in ISO standards and very good background evaluating & auditing suppliers to validate process and/or DOE.
• More than 15 years of engineering experience in Manufacturing & Quality Eng. dealing with computers, semiconductor, Class I & II medical devices, process & product development. • Provided documents for Build Tree, Process Flow, DMR, DHR, SOP, MPI’s for medical and electro mechanical devices using MS Word, MS Visio, Solid Works, and Adobe Photo Shop. • Qualified in using hand & power tools & electronic test equipment (e.g....
Seeking a position in Industrial, Manufacturing, and/or Mechanical Engineering that utilizes my education, knowledge and experiences specifically in the fields of Engineering, Mechanical Design, Manufacturing, Quality Control and Quality Assurance.
ACCOMPLISHMENTS Provided 80% improvement of QA review of new / revised: Engineering Drawings, Inspection Checklists, First Article Inspections, and NCMR dispositions at bioMerieux. Improved Marlo Coil's "On Time Delivery" of Shipments by 20%, reduced "Dock to Stock" cycle time in Receiving from 25 days to 3 days, & upgraded multiple department processes. Performed Cross-Facility audits of Business Mgt. Systems @ 9 DRS plant...
Tags for this Online Resume: Internal Audits, Supplier Audits, Quality Assurance, ASQ Certifications in Auditing, Engineering & Management, Interfacing with Regulatory Agencies and Customers, ISO 9001 Implemenation, Quality Catalyst, Management, Manufacturing / Assembly, Quality Management, Documenting Processes, Engineering Changes, Dispositioning Nonconformances, Contract Review
Summary: Bringing excellent experiences from 25 years of working as Development Engineering NPI Engineer, Manufacturing NPI Engineering, System Test Engineer/ Manufacturing Product Engineer, Quality Engineer, Supplier Quality Engineer and NPI Pilot Line Supervisor in Semiconductor Capital Equipment: * Project managed the transfer of prototype products (R&D) from concept to full production via build verification in NPI Pilot...
I am Yashica, working as a Regulatory Affairs Specialist and open for new job opportunities. I possess Masters Degree in Regulatory Affairs and have a working experience of Two Years (Plus a research Experience in Regulatory and Clinical area for two years). I am able to work in a Matrix and fast paced environment where one needs to prioritize the tasks and complete in a timely manner. I have handled projects independen...
languages. Responsible for written investigation of Non-Conforming Products (NCMR) and coordinated with Quality Management, Production, and Research & Development Engineers on implementation of corrective and preventive actions. Responsibilities included daily update of NCMR using Excel Spread Sheets, weekly inspection production areas, and verification personnel compliance with current operational procedures. Responsible f...
Summary of Qualifications Manufacturing engineering, experienced in both Research and Development (R&D) and operations. Generated Protocols and reports documenting validation of manufacturing equipment and processes to satisfy both FDA and CE requirements (e.g., IQ, OQ, PQ, ). Participated on a R&D team that brought new products to market from concept to finished goods. Conceptualized automation of a syringe manufacturing l...
Self-motivated and analytical Quality Professional with 20+ years of exceptional expertise in successfully managing quality and engineering operations, driving process improvement effects, and implementing policies within diverse and dynamic environments.