Programmer: MedFocus
PROGRAMMER COMPANY INFO: MedFocus offers clinical research contract outsourcing and staffing specifically to the pharmaceutical, biotechnology and medical device industries. We specialize in the nationwide recruitment of clinical trials personnel. Our client has committed themselves to high standards of integrity in contributing to the best ... more
Type: Full Time Location: San Francisco, CA Country: United States Posted: 11/18/2009 1:13:05 AM
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PHARMACY TECHNICIAN - Training Available NOW: Medical Careers Online
Pharmacy Technician
Pharmacy Technician - Training Available Training ... more
Type: Full Time Location: Industry, CA Country: United States Posted: 11/18/2009 1:13:04 AM
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DIALYSIS TECHNICIAN - Training Available: Medical Careers Online
Dialysis Technician Dialysis Technician - Training Available Dialysis tech salaries range from $23,830 to $31,733, nationally, according ... more
Type: Full Time Location: Visalia, Country: United States Posted: 11/18/2009 1:13:03 AM
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The Business Of Marine Biotechnology
Responsibilities and Requirements : Candidates must have a PhD in a biotechnology-related area and are expected to conduct research in marine science laboratories at the University while pursuing a professional MBA degree in the University Cameron School of Business. The goal of this 35 month program is to produce individuals ... more
Type: Full Time/Contract Location: Wilmington , NC Country: United States Posted: 11/17/2009 2:26:47 AM
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Transactional Biotech/Life Sciences Attorney
Research Triangle Park office seeks a senior transactional biotech/life sciences attorney to work at partner-level and head the transactional life sciences practice. Substantial experience in the areas such as biotech and other pharmaceutical collaboration agreements, licensing, life sciences related M&A, corporate partnering, and pharmaceutical and medical device development essential.
... more
Type: Full Time/Contract Location: Research Triangle Park , NC Country: United States Posted: 11/17/2009 2:26:47 AM
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Transactional Biotech/life Sciences Attorney
Tysons Corner office seeks a senior transactional biotech/life sciences attorney to work at the partner level. Substantial experience in biotech and other pharmaceutical collaboration agreements, licensing, life sciences related M&A, corporate partnering, and pharmaceutical and medical device development required.
We?d love to speak to you about this position. ... more
Type: Full Time/Contract Location: Tysons Corner, VA Country: United States Posted: 11/17/2009 2:26:47 AM
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Biotech Partner
Los Angeles law firm seeking biotech partner must have a degree in Biology, Chemistry or similar field. Experience in biotech patent prosecution and counseling, and significant portable business required.
Here's a prestigious L.A.-area law firm with a strong emphasis on what is probably the most sought after practice of ... more
Type: Full Time/Contract Location: Los Angeles , CA Country: United States Posted: 11/17/2009 2:26:46 AM
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Biotech/Biochem Patent Agent
Washington, DC office seeks a biotech/biochem patent agent with 4 years of experience with the U.S. Patent and Trademark Office. A technical background in biotechnology and/or biochemistry is ideal. A Ph.D. in biotechnology, biochemistry or a related science is required. Law firm IP experience is a plus.
This firm ... more
Type: Full Time/Contract Location: Washington , DC Country: United States Posted: 11/17/2009 2:26:46 AM
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Biotech Patent Agent/Attorney
Portland office seeks a biotech patent agent or associate with 3+ years of experience in drafting biotechnology opinions and drafting and prosecuting biotechnology patent applications. An advanced degree in biotechnology, pharmacology, and/or life sciences is required. Must be registered to practice before the USPTO. Ideal candidates should have a Ph.D. ... more
Type: Full Time/Contract Location: Portland , OR Country: United States Posted: 11/17/2009 2:26:45 AM
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Safety Clinical Research Associate II
Responsibilities : Exciting opportunity with the world leader in Heart Valves to advance patient care through clinical research on our Transcatheter Heart Valve Program. As a Senior Safety CRA, you will be responsible for the following: - Adverse Event handling and reviewing, according to SOP, European and FDA regulatory requirements. ... more
Type: Full Time/Contract Location: Irvine , CA Country: United States Posted: 11/17/2009 2:26:36 AM
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Clinical Research Associate
Responsibilities and Requirements : Master's Degree in Clinical Psychology with five (5) years of clinical research experience OR a PhD in a related field required. Ability to function independently in a clinical research setting. Ability to handle multiple, time dependent tasks. Excellent clinical skills in working with families and children. ... more
Type: Full Time/Contract Location: Philadelphia , PA Country: United States Posted: 11/17/2009 2:26:35 AM
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Biostatistician
Responsibilities:A leading Fortune 500 Pharmaceutical client of ours has an immediate opening for a Biostatistician based in East Hanover, NJ Job Description : Works with senior biostatistics staff and clinical monitors on clinical development plans, the design and conduct of clinical studies and in the evaluation,the design and conduct of ... more
Type: Full Time/Contract Location: East Hanover , NJ Country: United States Posted: 11/17/2009 2:26:28 AM
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Productivity Engineer
Be part of an energetic team whose mission is to improve the productivity of R&D engineers and the technical teams who support them, accelerating the development of leading-edge instrument products within Agilent's Electronics Measurement Group. In your role you will focus on Printed Circuit Board (PCB) layout and post-processing. ... more
Type: Full Time/Contract Location: Santa Rosa, CA Country: United States Posted: 11/17/2009 2:23:01 AM
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Senior Analytical Chemist/Senior Scientist
This is an experienced laboratory position requiring demonstrated application of principles, theories and techniques of biotechnological analysis to solve specific biopharmaceutical/biologics drug development problems. The position requires independent thinking, technical expertise, ability to perform complex work, and potential supervisory responsibilities.
... more
Type: Full Time Location: West Chester, PA Country: United States Posted: 11/17/2009 2:17:44 AM
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Administrative Assistant
Overview :
This position is a temp to permanent hire.
Responsibilities :
Heavy calendar management, the coordination of both domestic and international travel arrangements, coordinating logistics for office visits, meetings and division functions and ... more
Type: Full Time/Contract Location: Redwood City, CA Country: United States Posted: 11/17/2009 2:17:35 AM
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Senior Director, General Accounting
This position will be required to provide sound leadership and direction to our Accounting organization. The successful candidate will be required to partner with our senior leadership team to develop and implement strategies within the organization. Key roles of this position will include, but not limited to, operational reporting, compliance, ... more
Type: Full Time Location: Morgantown, WV Country: United States Posted: 11/17/2009 2:17:27 AM
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Chemist
This challenging entry-level position will be responsible for performing pharmaceutical testing including, but not limited to, HPLC, GC, TLC, UV, dissolution and IR spectroscopy.
Duties may include but are not limited to:
Performance of testing for development, validation, scale-up and/or stability of pharmaceutical products
Critical ... more
Type: Full Time Location: Morgantown, WV Country: United States Posted: 11/17/2009 2:17:27 AM
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Sr. Automation Engineer
Our Client - Fortune 500 pharmaceutical co, with sales of $ 4+B and 12K+ people, needs a Senior Automation Engineer for their packaging operations at their Corp. HQ/plant location. ++ Salary + bonus with relocation.
... more
Type: Full Time/Contract Location: N/A, Country: United States Posted: 11/17/2009 2:16:37 AM
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Associate Regulatory Affairs Specialist
Associate Regulatory Affairs Specialist
Under general supervision of Regulatory Affairs Manager, this person will help prepare and maintain submissions to regulatory agencies and required compliance reports, such as Drug Master Files (DMF’s), Annual Updates and amendments to the DMF’s in compliance with ICH Q7A and 21 CFR 314. ... more
Type: Full Time/Contract Location: N/A, Country: United States Posted: 11/17/2009 2:16:35 AM
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Validation Specialist
Validation Specialist
This person is responsible for preparing and executing validation qualification protocols for cGMP products, processes, production and laboratory equipment in compliance with Q7A and writing final reports for executed validation protocols.
Duties Include:
Reviewing of equipment manuals/technical ... more
Type: Full Time/Contract Location: N/A, Country: United States Posted: 11/17/2009 2:16:32 AM
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