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Online Resumes with "Iso Compliance"
Extensive experience in Supervising the Receiving and Shipping operations for a Medical Devices division of Johnson & Johnson. Excellent background in Worldwide Transportation. In-depth knowledge of DOT, FDA, GMP and ISO Compliance. Skilled in coordinating distribution activity among multiple U.S. and International operations. Bi-lingual Spanish/English.
Provide leadership by example with communication and accountability for all levels with solid agressive objectives for all metrics with workplans and training of all personnel to ensure P&L objectives are achieved as well as ongoing growth with the business plan.
I have been an engineering assistant along with working with many levels of personnel from a CEO to maintenance. I have written standard operating procedures to maintaining patent files and correspondence. I have experience in leadership along with many computer skills. I am dedicated, hard working and very punctual, with many years of perfect attendance. I’m a friendly team player and take pride in my work and doing a job ...
A Senior Supervisory position with 13 years of experience utilizing my excellent LEAN, leadership, problem-solving and communication skills in the manufacturing, logistics, or service-related industries.
Tags for this Online Resume: Manufacturing Supervisor
I need to be on the move all the time, problem solving, managing outside vendors, scheduling work, talking to customers.
MIKE ANDERSEN, C.P.M 7746 105th Avenue (262) 697-1813 Pleasant Prairie, WI 53158 firstname.lastname@example.org CAREER PERSPECTIVE An accomplished C.P.M. and Global “Supply Chain” control manager having the ability to negotiate cost as well as analyze quality improvement projects; partnering with local to off shore sources; using FAR, FDA and ISO polices and procedures. I continue to utilize my extensive procurement backgr...
A position where my skills in production and people management are needed.
Focused, can-do professional leveraging education and experience to procure goods and services at best cost and shortest lead times without sacrificing quality. Consistently achieves on-time delivery through continuous supplier improvement initiatives in shorter setup times, smaller lot sizes, and conformance quality engineered into manufacturing process. Collaborates across the organization to consistently maintain supply ...
Useful & Effective Media: Technial Writer & Editor, Project Leaders, UI Architect for Print, On-line, & Web-based content
I am looking for a writing and/or editing role in which I can also use my project leadership and keen sense of useful web-based architecture skills.
Tags for this Online Resume: effective, persistent, smart, useful, clear, FrameMaker, Visio, MS Office, HTML, Photoshop, Dreamweaver, SalesLogix, Documentum, SAP, FileMaker Pro, FTPPro, Lotus Products, Acrobat
I am looking for a position in the medical device industry involving hardware or software verification and validation, quality engineering, documentation, design planning and control, FDA or ISO compliance.
Experienced Quality Manager with a proven record of developing the methodologies and tools to help companies manage organizational change, meet customer requirements and provide product excellence. Has extensive project team and department management experience in Quality Management and Regulatory Engineering, primarily for information systems, telecommunications and medical applications. Highly analytical, dynamic, resul...
Tags for this Online Resume: Program and Project Management, Business Analysis/Process and Data Analyst, Software Quality Assurance (SQA),, Requirements Management, Configuration Management, Defect Management, Quality Systems Development and Quality Management, Business Process Vision and Policies, Organizational Development and Re-engineering, Business Systems Requirements Specification, Course Development and Technical Training, Process and Training Documentation and Technical Writing, Product Design and Qualifications (power and packaging), Component Engineering (analog and materials), European and Asia Pacific business experience, Data Base Development and SQA, Use Case Modeling, Requirements and Defect Management, Issue Management, Document Management, KPI Definition, Analysis and Business Process Improvement, Use Cases Development, Test and Training, Internal Audit Planning, Implementation and Management, Hardware and Software PLC Management, Software Development Life Cycle (SDLC), Product Safety, EMC, EMI Environmental Management, Manufacturing, Customer and Field Support, Standards and Regulatory: UL, CSA, IEC, ISO, VDE, BSI, KEMA, FCC, FDA, PTT, BABT, OSHA, NEC, Sarbanes-Oxley (SarbOx/SOX), COBIT, Standards Making Committees: ECMA TC12, CBEMA ESC2, TIA, Process Frameworks: ISO 9000:2000 and TL 9000 (cGMP/QS9000 equivalent), CMMI, ITIL, SWBoK, PMBoK, RUP, and Sarbanes-Oxley compliance, Mass Quality Award/Baldridge Evaluation/Implementation, ODI and Rummler-Brache Process Improvement Methods, Metrics and Tools: TQM, SPC, TL9000 and GR-929 metrics implementations and Six Sigma tools and methodologies