| Tuesday, May 01, 2012 | | | | |
Laboratory & Pharmaceutical Equipment: Surplus to Ongoing Operations of Sanofi-Aventis!
Please click here for more information. | More Top News | Please Join Aptuit at their Medicines Research Centre in Verona Italy
Drug Discovery and Development is an expensive and high-risk business that can take 10 years from inception to the commercialization of a new drug. Often associated with high attrition rates, it is driven by medical need, disease prevalence and likelihood of success. Drug Development has traditionally been a long and extensive process designed for a staged assessment of the safety, efficacy and manufacture of a drug candidate. On May 16, 2012, Aptuit will welcome nine distinguished representatives from academia and industry to speak at this FREE symposium where they will cover and discuss aspects and strategies to reduce risk, costs and timelines from Candidate Selection to Phase II Clinical Trials.
For a full description of this event, and to register, please go to: www.aptuit.com/verona/paradigms/introduction.aspx. | | More Featured News | SafeBridge Consultants, Inc. announces two Potent Compound Safety Training offerings (may be taken separately or consecutively)
The SafeBridge original Potent Compound Safety "Boot Camp"® (Boot Camp I) is a comprehensive two-day course in pharmaceutical potent compound safety focused on training EH&S and related professionals in critical technical concepts and proactive safety programs in pharmaceutical industrial hygiene, occupational and environmental toxicology, analytical chemistry, and risk communication.
The SafeBridge Advanced Concepts to Support Drug Development of Potent Compounds from R&D through Manufacturing (Boot Camp II) is a one-day advanced course focused on case studies and problem-solving to address potent compound safety issues in discovery, development, contract manufacturing and commercialization.
COURSE SEATING IS LIMITED AND USUALLY SELLS OUT!
San Diego, CA Boot Camp I May 15-16, 2012 Boot Camp II May 17, 2012
Contact: Susan Custer: susan.custer@safebridge.com or 650-961-4820 x 231 or www.safebridge.com. | | Drug Delivery Partnership Strategies
• Learn from interviews with senior drug delivery partnering executives. • Develop effective partnering strategies based on case studies and analysis of market data. • Unlock therapeutic value of new biopharmaceutical developments by strategic collaborations for innovative drug delivery technologies.
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! | • Biotech Beach (Irvine, California)
Aviir, Inc. Research Scientist Will play a key role in the program initiation, downstream development, optimization and implementation of new process in key technical areas, including sample preparation and analysis (qPCR & sequencing). This position will work closely with Clinical Operations groups in supporting the transfer of new technologies to the production environment and ensuring their successful deployment.
• Pharm Country (Farmingdale, New York)
Astellas Pharma US Research Quality Assistant Director Work with internal research stakeholders across multiple geographical locations to ensure adoption of and compliance with corporate policies on quality assurance for research studies. Ensure that studies are conducted and the data collected in compliance with approved protocols, appropriate corporate guidelines, internal work procedures and industry regulations and standards.
• BIoMidwest (Gurnee, Illinois)
Watson Pharmaceuticals, Inc. Material Handler I Under close supervision, performs duties necessary for compliant receipt, storage and customer order processing of finished goods, raw materials, supplies and completing inspections and packaging of customer orders prior to shipping, including controlled substances.
• Genetown (Cambridge, Massachusetts)
Vertex Technical Operations Manager Will partner with late-stage product development teams in order to ensure that process and product development activities result in commercially relevant processes with robust design space features.
• Rocky Bio (Tucson, Arizona)
Ventana Medical Systems, Inc. Director, Regulatory Affairs Responsible for leading the day-to-day activities of Regulatory Affairs with specific emphasis on global regulatory submission strategy, regulatory submissions, and interaction with global regulatory authorities related to companion diagnostic projects.
Get Noticed! Add your resume to the BioSpace Career Center! See more than 5,000 job postings in the BioSpace Career Center! | |
Pharm Country Career Fair
Job seekers can spend a day with HR representatives and Hiring Managers from top biotech, pharma, medical device and diagnostics companies in the tri-state area.
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.
• Pharm Country Career Fair, King Of Prussia, PA May 1, 2012 • BioNC Career Fair, Durham, NC May 2, 2012 • Biotech Bay Career Fair, Burlingame, CA May 29, 2012
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 | | Coldstream Laboratories Inc. 1500 Bull Lea Road, Suite 250 Lexington, Kentucky 40511 U.S.A. Phone: 859-257-6600 Fax: 859-323-5985
At Coldstream Laboratories Inc. (CLI), we're seasoned at turning pharmaceutical development ideas into safe, pure, and effective clinical pharmaceutical dosage forms. Since 1986, we have completed more than 200 formulation development projects that led to clinical trials providing us extensive clinical manufacturing experience with both commercial product development and grant-funded projects from such sources as the National Institutes of Health.
More Company Profiles | | | FREE Subscription to Pharmaceutical Executive
Pharmaceutical Executive is a publication designed to meet the diverse management and marketing needs of professionals in the pharmaceutical industry worldwide. Editorial provides useful information on marketing, sales and promotion, as well as legal and regulatory issues. |
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BioSpace.com - Life. Science. Community. | | • BioSpace is a registered trademark of BioSpace, Inc. • Please distribute this e-cast freely. • Credit any excerpts as follows: Copyright 2012 BioSpace http://www.biospace.com • While BioSpace and its agents used their best efforts in collecting and preparing the information published herein, we do not assume, and hereby disclaim, any liability for any loss or damage caused by errors or omissions, whether such errors or omissions resulted from negligence, accident or other causes. | | | | | | |
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