| Tuesday, December 13, 2011 | | | | |
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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.
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PolyMedix, Inc. Vice President Regulatory Affairs Will report to the CEO and will supervise the planning and coordination of clear and effective regulatory submissions and ensure that the regulatory strategy meets the development requirements for our products.
• Biotech Beach (Santa Monica, California)
Astellas Pharma US Research Associate/Senior Research Associate: Antibody Drug Discovery Responsible for in vitro target validation activities and monoclonal antibody (MAb) screening. The primary function of this position is to assist in antibody drug conjugate discovery efforts. Characterization and functional validation of therapeutic MAbs in a variety of cancer relevant cell-based in vitro assays will be a major emphasis.
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Baxter International, Inc. Senior Director, Regulatory Affairs Guides, directs and coordinates the strategic planning of the Regulatory Affairs advertising and promotion function. Applies strategic direction, critical review skills and creative solutions to diverse promotional scenarios.
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Seattle Genetics, Inc. Process Sciences Project Manager Responsible for project management of the CMC portion of our clinical development programs. The job includes serving as the project manager for the CMC subteams involved with our clinical development programs, management of the Technical Development Committee which oversees all of the CMC subteams, and providing management assistance with our yearly and long-range planning budget cycles.
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Watson Pharmaceuticals, Inc. Manufacturing Engineer I Under general supervision, assists in troubleshooting the manufacturing and packaging areas. Provides technical support to all departments in the areas of equipment operation and process improvements.
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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.
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