Tuesday, March 27, 2012

Bausch & Lomb to Shell Out $500M for ISTA - Mar. 27, 2012

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Challenging Current Paradigms in Early Drug Development

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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.

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Don't Miss This

The Pharmaceutical Compliance Forum (PCF) International Pharmaceutical Compliance Congress, www.InternationalPharmaCongress.com, May 14-16, 2012, takes place at the Hilton Budapest in Budapest, Hungary and features tracks on EU, CEE, MEA, global compliance audits and monitoring, FCPA and global anticorruption, global transparency, discourse and aggregate spend and global compliance case studies.

For more information, please visit: http://internationalpharmacongress.com/.
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Event of the day

Value-driven Engineering: A National Conference on Medical Innovation and US Global Competitiveness
April 22-24, 2012
John S.Knight Center
77 E. Mill Street, Akron, Ohio
Event Website

Join us April 22-24, 2012 for the Value-driven Engineering National Conference on Medical Innovation for U.S. Global Competitiveness. Value-driven Engineering is a national effort launched in 2011 that actively engages our nation's thought leaders in various sectors to explore the promise of maintaining our country's competitiveness through a medical device development strategy that focuses on product design based on patient need, resource optimization and efficiency. During the conference attendees from industry, academia, government, and public and private sectors will focus on developing the Value-driven Engineering equation, analyzing the components necessary for Value-driven Engineering, exploring real-world examples of Value-driven principles and promoting public-private engagement of the Value-driven Engineering strategy. A Call for Case Studies has been released. 3-5 case studies will be awarded $1,000 and an opportunity to present at the conference. One of the finalists will also be awarded a grand prize $2,500 at the conference.

Learn more by visiting our website at www.abiakron.org/national-vde-conference-akron-ohio.
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Top Jobs
Genetown (Boston, Massachusetts)

Takeda Pharmaceuticals
Director/Sr. Director, Regional Search & Evaluation
Responsible for working closely with other relevant functions within the broader Takeda organization to (i) develop a BD strategy consistent with the core therapeutic area R&D and commercial strategies outside of oncology and vaccines (ii) identify and triage opportunities consistent with the agreed strategies and (iii) lead cross-functional due diligence teams to efficiently assess and prioritize in-licensing and alliance opportunities across the R&D pipeline.

BioMidwest (Chicago, Illinois)

Takeda Pharmaceuticals
Manager / Associate Director, Regulatory Strategy
Plans/manage/executes all regulatory activities of all levels of complexity for project of responsibility in development and/or supports regulatory activities for assigned marketed product of responsibility.

Genetown (Woburn, Massachusetts)

EMD Millipore
Research Scientist III
Will develop, transfer, and validate analytical methods to support Upstream Processing development projects such as chemically defined mammalian cell culture media. As such, the candidate will be expected to provide analytical leadership on project teams within the matrix organization and coordinate all analytical activities in support of product development.

Pharm Country (Parsippany, New Jersey)

Watson Pharmaceuticals, Inc.
Department Coordinator II
Maintains regulatory affairs objectives complementary to corporate policies and goals. Request documents and formats data from other departments in a comprehensive package as directed by supervisor for inclusion in submission. Supports maintenance of regulatory affairs information databases to track various statuses of projects. review.

Biotech Beach (La Jolla, California)

Pfizer, Inc.
Technical Associate/Specialist
Participate in routine handling, feeding, transportation, and care of laboratory animals including daily washing, cage change, cleaning, and transportation of animal cages. Ensure that normal housekeeping duties are performed and cleanliness is maintained in the animal work area.

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BioSpace Career Fairs

Biotech Beach

Biotech Beach 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 Southern California 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.

Biotech Beach Career Fair, La Jolla, CA April 17, 2012
BioCapital Career Fair, Bethesda, MD April 25, 2012
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

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Company of the day

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.

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