| Thursday, October 13, 2011 | | | | |
The Master of Science (MS) in Medical Product Development Management (MPDM) 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.
Please click here for more information. | 4 Common Mistakes That Sabotage Your Resume By Anish Majumdar, Certified Professional Resume Writer
Developing an effective resume can be a daunting task. How do you summarize the most relevant aspects of your career within 1-2 pages? Which details should be included and which saved for the interview? How do you know if your document is really working or getting rejected out-of-hand?
The following 4 "Resume Killers" are common mistakes I've encountered in working with clients as a Certified Professional Resume Writer. If your resume suffers from one of the following, I'd recommend a re-write before continuing with your job search: More...
More Features | | | • Biotech Bay (Novato, California)
BioMarin Pharmaceutical Inc. Senior Associate/Mananger, Regulatory Affairs CMC Improve your resume for this job, click here. Focuses on managing the regulatory CMC aspects of both BioMarin commercial and development projects domestically and internationally. The role requires numerous interactions with in-house CMC project teams, external partners, contract manufacturing organizations, and global health authorities to ensure rapid review and approval of the CMC portions of BioMarins marketing applications, supplements/ variations, clinical trial applications and other CMC-oriented filings
• Biotech Beach (San Diego, California)
Elevation Pharmaceuticals Research Associate Improve your resume for this job, click here. Responsible for assessing the performance characteristics of drug formulations with drug delivery device. He/she will make detailed observations, analyze data and interpret results with minimal guidance. The candidate will also document data in manner that can be used toward patent filing. He/she will prepare technical reports, summaries and quantitative analyses of assigned research projects.
• Pharm Country (Hawthorne, New York)
On Assignment Clinical Research Drug Safety Associate Improve your resume for this job, click here. Responsible for the collection, documentation and processing serious adverse events from clinical trials and all adverse events from post marketing spontaneous reports in accordance with Federal Regulations and the company's Standard Operating Procedures.
• Bio NC (Rocky Mount, North Carolina)
Hospira, Inc. Lead Auditor Improve your resume for this job, click here. The Lead Auditor coordinates, administers, and implements the quality systems audit program to assure the product is manufactured in compliance with established regulations and Hospira quality policies.
• BioMidwest (Deerfield, Illinois)
Baxter International, Inc. Senior Manager, BioScience Specialty Therapies/Corporate Development Improve your resume for this job, click here. Responsible for leading less complex business development opportunities through the deal phase. Manages the research and analysis of the business opportunities and assesses potential markets.
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• Get Noticed! Add your resume to the BioSpace Career Center! • See more than 5,000 job postings in the BioSpace Career Center!
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Bio NC 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 south east region.
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.
• Bio NC Career Fair, Durham, NC October 20, 2011 • BioCapital Beach Career Fair, Bethesda, MD November 1, 2011 • Genetown Career Fair, Cambridge, MA November 7, 2011
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 | Drug Discovery & Development
Drug Discovery & Development magazine delivers vital insight about the latest technologies and tools used to develop pharmaceutical products to key decision-makers
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