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Online Resumes with "equipment qualification"
Seeking Pharmaceutical QA Position - - Full Time or Consulting Position SR. PHARMACEUTICAL QUALITY SYSTEMS AND VALIDATION PROFESSIONAL with a broad knowledge of regulatory compliance and quality control and assurance expertise in cGMP manufacturing, operations, regulatory, supply chain management, and validation as applied to aseptic parental pharmaceutical products, tablets, APIs, and medical devices. My experience in...
Tags for this Online Resume: North Carolina, South Carolina, Florida, Texas, Missouri, Chicago, Atlanta, Associate Director of Quality Assurance, Quality Assurance Manager, Sr. Compliance QA Manager, Associate Director of Validation, Validation Director, CAPA Management, Supplier QA Manager, Director of Supplier Assurance, CMO QA Manager, Pharmaceutical QA Manager, Medical Device QA Manager, Corporate QA Auditor, CAPA Manager, API Manufacturer, Sterile Fill Pharmaceutical Manufacturer, Medical Device Manufacturer, Sr. Quality Engineer, Oklahoma, Illinois, Milwaukee WI, Validation Manager, Internal QA Auditor
Seeking an engineering position in the San Diego area where my six years of management and engineering experience with new product development, process and equipment qualification, and operations management can be fully utilized. I am a team leader and team player with the ability to demonstrate these skills in any environment.
I want to find a company where I can spend many years being part of the organization growth and expansion.
Professional with exemplary record in providing Packaging Lines/Process Systems in support of new product presentations and product launches, and improving packaging line and process system efficiencies utilizing Six Sigma Lean Manufacturing concepts. As an astute and organized problem-solver creating solutions and bringing together various groups to have a common consensus and agreement.
PROFESSIONAL SUMMARY Skilled engineering professional with over thirty years of structural and mechanical engineering, nuclear power and commercial design experience. Broad technical expertise in structural mechanics, seismic design and analysis, seismic equipment qualification (SEQ) as well as in design and evaluation of pressure vessels, piping and pipe supports. In-depth knowledge of industry codes and standards, includi...
Tags for this Online Resume: Pipe Support, Power (Os Enhancemnt Tool, Consulting, Engineering, analysis and design, Mechanical Engineering, Support, Technical Support, Structural Engineering, AISC, ASME
CNC Machinist Work well with others and alone. Supervisory experience, motivated and a lot of experience in the machining industry. JOB HISTORY/DUTIES CNC Specialist Orluck Industries, Elk River, MN ELK RIVER, MN Start Date: 05/2010 End Date: 02/2015 Set-up and operate the various pieces of CNC equipment available. Effectively operate a variety of vertical and horizontal machining centers and turning centers. Orluck Industr...
SUMMARY: * More than 21 years of excellent experience in Medical Device & Pharmaceutical companies in the area of Process engineering, process Validations, Equipments Qualifications (IQ/OQ/PQ), Process Development Cleaning Validations, New Product Developments, Product and process Technology transfer, Troubleshooting Processes, and in Medical Devices, Product Testing. * Extensive experience in Quality assurances: Auditing, ...
I as exceptionally good at building new product production (electronic manufacturing) from the ground up. Equipment selection, characterization and qualification. Process development, qualification, all the way to manufacturing qualification , training , and production.
Tags for this Online Resume: Process engineerinjg, SPC, Equipment Qualification, Process Qualifcation, SMT, Flip chip, Manufacturing qualification, Semiconductor MEMS, Assembly Line, Lasers, Information Technology, Electronics, Wire Bond, Cu Au Al, Packaging, Failure Analysis, Motorola, Test, Engineering, Flip Chip (FC), Manufacturing, 12 Volt, Audio
WORK EXPERIENCE SUMMARY Lead Electrical Engineer At Shearon Harris Nuclear Plant (Duke Energy), I was the lead electrical engineer for developing FLEX strategy and provide generate electrical design and testing document to meet NRC requirements. This project was successfully completed on May 31st of 2015. Procedure Writter Developed Fire protection procedures at plant Vogtle 08/2012 - 12/2012 QA manager Tri-En Corporation a...
ACCOMPLISHMENTS * Accounting Skills: I can operate computers programmed with accounting software to record, store, and analyze information. * Accounting Reviews: I can conduct detailed technical and analytical review of federal/state corporate, partnership and S corporation tax returns, provisions, and quarterly estimates prepared by associates. * Auditing: I have experience with Financial Statements audits, reviews, compil...
Project Oriented Professional with 25 years' experience in hardware/software design test and release to manufacturing. Call Center Sales Client Sales Kaizen Value-Stream Mapping 5S Environment Lean Six Sigma Continuous Improvement. AREAS OF EXPERTISE * Project Management - PMP Certified * Project Management -Instructor * SCRUM Master & Developer * SCRUM - Instructor * Risk Management - Instructor * Lean Six Sigma * Green Be...
QA Manufacturing Compliance Lead Lead QA Validation Remediation - Comprehensive Product and Process gap assessments of HVAC, Utility Maintenance programs, product Scale-up through commercial validation, packaging and manufacturing process failures, and customer complaints for Prescription, OTC & DEA products. Conduct review of CMO validation change control and QC OOS/OOT reports and write annual Product Review for all produ...
Tags for this Online Resume: Training, Project Management, Distribution, Management, Risk Management, CFR Part 11, Design Specification, pharmaceutical, protocol, Leadership, Staff development, cleaning validation, process validation, computerized systems validation, Program Management, QC testing, Chemist, CAPA, NCR, Customer Complaints, Supplier Quality, commissioning, equipment qualification, equipment purchase, Change control, Auditing, Medical Devices class I, II and III, Pharmaceutical development DOE, Pharmaceutical Clinical Scale-up, Mfg./Pkg. Management, ISO13485, Technical Reporting, FDA site QA contact