 | | Friday, June 22, 2012 |  | | | |  |
Choose a CRO Partner Who Understands Your Unique Development World.
Whether you're investigating an apparatus, instrument, machine or other type of device, our Medical Device Business Unit knows your success hinges upon highly specialized regulatory, reimbursement programs, safety and marketing support. Operating on high-quality systems, we can prepare those key documents that will ultimately clear your product for marketplace entry.
Even after your commercial launch, we're here to help propel your device to that next level. From developing a reimbursement strategy to meeting post-marketing surveillance requirements, we offer the added value of a long-term relationship that endures throughout every phase of your device's lifecycle.
Visit Theorem to find out more. | 
More Top News | 
FIME 2012 International Medical Expo
August 8 - 10, 2012
Miami Beach Convention Center
Miami, Florida
Organized at Miami Beach Convention Center, Florida, USA, the FIME International Medical Expo (FIME) is one of the prioritized event for medical fraternity. It is 3 days which is aimed towards welcoming more than 29,000 visitors. Some of the exhibited items include branded drugs, blood bags, diagnostic equipments, gynecological equipments, needle holders, operating tables, oxygen products, surgical blades, refurbished medical equipments, incubators etc. The event emerges out as a fulcrum point and attracting worldwide buyers, sellers, retailers, wholesalers etc. | | 
The Master of Science (MS) in Medical Product Development Management (MPDM) at San Jose State University is a comprehensive, master's degree program and can be completed in either 2 or 3 years. The emphasis of the program is on the management of products undergoing clinical research and clinical development, i.e. clinical trial stages I, II, III and IV or other testing as required by the Federal Food and Drug Administration (FDA) or international regulatory authorities.
The curriculum includes customized courses from the Colleges of Science and Business, and was designed in consultation with biomedical industry employers in the greater San Francisco Bay area. The MPDM program continues to have interaction with the industry and provides expert industry speakers in the classroom, in order to present the latest advancements to students.
For more information, please visit: http://www.medproddev.sjsu.edu/. | | 
More Featured News |  • Pharm Country (King of Prussia, Pennsylvania)
Tunnell Consulting
Manufacturing Process Engineer
Responsible for incorporating robust and sustainable facility custodial maintenance solutions (Plant infrastructure cleaning & sanitization) that will improve the compliance profile at the Lancaster site. This individual will evaluate the current custodial processes (cleaning chemicals and procedures) and optimize them accordingly.
• Biotech Bay (Santa Clara, California)
Abbott
Software Engineer / Senior Software Engineer
Develop UI Software for a medical device, participate in Software/ UI design activities.Write Specifications and design documents, unit tests. Participate in formal design reviews. Assist Software test team in developing Test cases and test plan.
• Genetown (Ipswich, Massachusetts)
New England Biolabs, Inc.
Quality Engineer
Reporting to the Director of Quality Management Systems, the Quality Engineer will be responsible for the routine execution and support of New England Biolabs Quality Management Systems ("QMS"), as well as, leading Quality and Operations System optimization efforts for the whole NEB community. Advanced level applications of Operational Excellence (OPEX) concepts, tools and techniques is required, in addition to, an excellent understanding of ISO 13485 and ISO 9001 Quality System compliance requirements.
• Biotech Beach (Corona, California)
Watson Pharmaceuticals, Inc.
Quality Assurance Engineer Principal
Will lead the Quality Engineering Group supporting the Quality Control Laboratories. Under limited supervision, analyzes quality issues in laboratories, and resolves complex work process and Laboratory issues. Provides support to Director in project coordination, problem solving, and designing process improvement solutions.
• Bio NC (Clayton, North Carolina)
Hospira, Inc.
Continuous Validation Engineer
Responsible for compilation and statistical assessment of in-process and final product data. The individual will also be responsible for coordinating and performing risk assessments. This individual will communicate and interact with all levels of the site and corporate hierarchy.
• Get Noticed! Add your resume to the BioSpace Career Center!
• See more than 5,000 job postings in the BioSpace Career Center! | | 
Job seekers can spend days with HR representatives and Hiring Managers from top biotech, pharma, medical device and diagnostics companies in various regions across the U.S.
Candidates with a 4-year degree in the life sciences and a minimum of 2-years of industry related experience are invited to attend. (Equivalent work experience may be considered in lieu of a four-year college degree. PhD and Postdoc candidates welcome.)
Exhibiting companies are recruiting for positions in areas such as: QA/QC, clinical research, engineering, manufacturing, biostatistics, clinical data management, chemistry, regulatory affairs, and research.
Job seekers may register here.
More information about BioSpace's Career Fairs
BioSpace White Paper
Biotech Career Fairs For Job Seekers 101: Control Your Experience
By June Salvati, BioSpace Director of Events and Corporate Services | | 
The Respiratory Diagnostic Devices Market Outlook to 2016
• Discover the epidemiology of key respiratory disorders with this report's forecasts through to 2016.
• Analyze the key challenges facing companies in the respiratory diagnostics devices and discover the responses to them from the leading players.
• Discover the key types and differentiating features of the most important respiratory diagnostic devices.
Click Here for More Information | |
Building Novel Applications with Pipeline Pilot to Drive Next Generation Sequencing
This case study shows how scientists are streamlining the process of analyses of DNA sequence information. Enabled by new DNA sequencing technologies, many more scientists and informaticians are interrogating larger and more complex data set.
Request Now! | 
LifeScan, Inc.
1000 Gibraltar Drive
Milpitas, California 95035 U.S.A.
Phone: 408-263-9618
LifeScan, Inc., a member of the Johnson & Johnson Family of Companies, is a global leader in blood glucose monitoring systems for home and hospital use. LifeScan has been committed to improving the quality of life for people with diabetes for over 20 years.
More Company Profiles | |   | FREE Subscription to Medical Design Briefs
Medical Design Briefs features exclusive coverage of the latest medical and bio-medical innovations from NASA, its industry partners, and other major players in medical R&D worldwide. |
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