Friday, April 27, 2012

Novo Goes on US Hiring Binge; Jazz Spends $650M Cash on EUSA - Apr. 27, 2012

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Top Stories 
•  Novo Nordisk A/S (NVO) Goes on US Hiring Binge More...
•  Jazz Pharmaceuticals, Inc. (JAZZ) Spends $650 Million Cash on EUSA Pharma More...
•  Ranbaxy Laboratories (RANBAXY.BO) Creates India's First New Drug More...
•  FDA Approves Novartis AG (NVS)'s Afinitor for Kidney Tumors More...
•  FDA Approves GlaxoSmithKline (GSK)'s Votrient® for Deadly Sarcomas More...
•  FDA Rejects Amgen (AMGN)'s Application for Xgeva More...
•  FDA Warns Not to Mix Merck & Co., Inc. (MRK) Hep C Drug With HIV Meds More...
•  Could Bristol-Myers Squibb Company (BMY) be a Target of Bribery? More...
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•  Nitric Oxide Supplementation Treats Common Metabolic Disease, American Journal of Human Genetics Reveals More...
•  Gene "Switch" Regenerates Damaged Heart Cells in Animal Study, Duke University Medical Center Reveals More...
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Top Jobs
Pharm Country (Somerville, New Jersey)

Heron Health
Director - Evidence, Pricing & Access
Ensuring that all projects are being conducted in an efficient manner and that quality and client satisfaction is maximized at all times, and that the direction of the project and quality of the deliverables meet both the project objectives and the client needs.

Biotech Beach (Santa Monica, California)

Astellas Pharma US
Environmental Health and Safety Officer
Will facilitate compliance with all applicable environmental, health, and safety principles, guidelines, and legal requirements; deliver, coordinate, and track lab safety training activities; create and maintain company safety practices and manuals; coordinate safety inspections and direct the EH&S program.

Rocky Bio (Salt Lake City, Utah)

Watson Pharmaceuticals, Inc.
Manager, Regulatory Affairs Proprietary
Under general direction, functions as primary regulatory contact with regulatory authorities for assigned products and projects. Manages preparation of regulatory submissions, briefing packages and presentations for regulatory agency meetings. Determines nature, scope and format of information to be generated in order to successfully: file and maintain INDs/CTAs; file regulatory dossiers; respond to health authority inquiries; maintain product registrations and obtain international market access.

BioMidwest (Chicago, Illinois)

Takeda Pharmaceuticals
Medical Director, Pharmacovigilance
Serves as the Global Safety Lead physician for complex, strategically important developmental programs especially those that are Phase III and IV programs. Responsible for the oversight of signal detection and risk management activities for designated global products. Ensures patient safety is adequately addressed in TGRD sponsored studies.

Genetown (Cambridge, Massachusetts)

AVEO Pharmaceuticals, Inc.
Scientist, Pharmacology
Will lead and participate in the evaluation of antibody drug candidates in relevant in vivo models of cancer including proof of concept, target validation, PK/PD relationships as well as efficacy.

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Pharm Country

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

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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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