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| Johnson & Johnson Family of Companies |
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PA |
11/19/2009
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| Principal Research Scientist (Data Warehouse Administrator) - Radnor |
| A minimum of a PhD is required with at least 5 years of experience. Knowledge of biology and/or clinical science in the therapeutic areas of interest (immunology, oncology, etc.) is required. Must have excellent communication skills, demonstrated leadership skills, and the ability to operate in matrixed and global environment. Technical expertise with bioinformatics and/or medical informatics applications is required. Must have experience with database development in commercial setting as well as experience with data mining algorithms and applying them to biological and/or clinical problems. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
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| Process Engineer/Scientist - Pharmaceutical Manufacturing Process Support |
| Basic Qualifications: Bachelor's degree in Chemical, BioChemical or Bioprocess Engineering with 7 years experience in a GMP Biopharmaceutical manufacturing or research and development environment OR Master's degree in Chemical, BioChemical or Bioprocess Engineering with 5 years experience in a GMP Biopharmaceutical manufacturing or research and development environment OR PhD in Chemical, BioChemical or Bioprocess Engineering Preferred Qualifications:Experience leading and developing people and teams Experience and expertise in protein purification or fermentation Project management experience Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. We offer an excellent salary and an industry-ranked benefits program, including tuition reimbursement, work-life balance initiatives and developmental programs at all levels. Merck's retirement package includes a pension plan and one of the best 401(k) plans in the nation. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # CHE002084. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Our work is someone's hope. Join us.Where patients come first - Merck Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
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| Sr. Engineer/Scientist - Manufacturing Process Technical Support |
| Minimum Qualifications: Bachelor's degree in Chemical, BioChemical or Bioprocess Engineering with 5 years experience in a GMP Biopharmaceutical manufacturing or research and development environment OR Master's degree in Chemical, BioChemical or Bioprocess Engineering with 2 years experience in a GMP Biopharmaceutical manufacturing or research and development environment Preferred Qualifications:Experience providing technical support of a GMP manufacturing process, specifically in protein purification and/or fermentation. Experience writing technical documentation: such as change controls, protocols, operating procedures. Experience with commissioning, qualification, and validation of biopharmaceutical equipment and processes. Demonstrated expertise in bioprocessing unit operations such as fermentation, chromatography, tangential flow filtration Demonstrated ability to lead a group of individuals in task oriented assignments such as technical investigations, root cause analysis, equipment installation Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. We offer an excellent salary and an industry-ranked benefits program, including tuition reimbursement, work-life balance initiatives and developmental programs at all levels. Merck's retirement package includes a pension plan and one of the best 401(k) plans in the nation. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # CHE002082. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Our work is someone's hope. Join us.Where patients come first - Merck Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Novartis Oncology |
na |
MA |
11/20/2009
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| Pathways Research Scientist (BS/MS) |
| ?BS or MS in Biochemistry, Molecular Biology, or Cell Biology, with 5+ years of laboratory research experience.
? Extensive experience with culturing various mammalian cell lines, utilizing both 2D and 3D culture systems, designing cell-based assays, generating stable cell lines, and executing small molecule screens with laboratory automation equipment.
? Experience with high content imaging and designing/executing high content imaging-based screens.
? Outstanding molecular biology techniques including complex DNA cloning, site-directed mutagenesis, and qPCR.
? Exceptional expertise in genetic screening with siRNA/shRNA/cDNA by conventional and viral transduction technologies.
? Proficient in various protein analysis techniques, including, but not limited to, ELISA assays, immunoprecipitations, and western blots.
?Excellent communication skills |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
11/19/2009
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| Scientist, Target Discovery -- Agensys, Santa Monica, CA |
| The successful candidate will have a PhD in molecular biology, biotechnology, biochemistry or related discipline with minimum 5 years of relevant industry experience. Other required experience includes expertise in a broad range of molecular and cellular techniques surrounding aspects of microarray-based discovery, biomarker identification and target selection for product development. Experience with management of research associates and demonstrated leadership is preferred. Excellent verbal and communication skills, as well as the ability to work in a dynamic team environment are essential. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
11/19/2009
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| Scientist/Sr Scientist, Translational Research -- Agensys, Santa Monica, CA |
| Candidate consideration requires a Ph.D. in molecular and cellular biology or similar field with a minimum of 6 years of post-doctoral experience. Industrial experience in Oncology drug discovery and experience managing research associates is highly preferred. Successful candidates will have strong written and oral communication skills, be self-motivated, demonstrate leadership and possess an exemplary record of research, as evidenced by publications and patents. Developmental opportunities include leading projects for therapeutic antibody discovery, building new technology platforms, and team leadership. |
| Vertex Pharmaceuticals |
San Diego |
CA |
11/19/2009
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| Research Scientist I (Medicinal Chemistry) |
| Minimum Requirements
? Ph. D. in organic synthesis with 0-3 years of productive, relevant post-doctoral experience or
? MS in organic synthesis with 3+ years of productive pharmaceutical experience or
? BS in organic chemistry with 6+ years of productive pharmaceutical experience
Vertex Pharmaceuticals |
| Novartis Oncology |
na |
MA |
11/20/2009
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| Histotechnology Research Scientist (BS/MS) |
| The ideal candidate will have a BS or MS degree in a biological or chemical science discipline plus at least 4 years of histology experience. Strong organizational skills, self-motivation, attention to detail, flexibility, proactive willingness and desire to engage in the laboratory workflow, and an ability to contribute to a team environment are essential. Candidates should have experience working in a fast-paced, high volume, high productivity and quality environment, in either an industry or clinical laboratory. Experience and proficiency with immunohistochemistry methodology and image analysis is strongly preferred. Prior experience in cell biology and/or molecular biology techniques is preferred. |
 AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
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| Senior Scientist - Neuroscience Biology |
·PhD plus minimum 2 years of post-doctoral research experience, demonstrated ability to implement independent research as evidenced by a strong publication record related to the desired core discipline.
Preferred Background:
·Behavioral Neuroscience or comparable discipline.
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| Novartis Oncology |
na |
MA |
11/20/2009
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| Group Head, Biochemical & Organ Toxicology (Cambridge) |
| We are seeking an experienced scientist and manager to lead a Biochemical & Organ Toxicology group within Investigative Toxicology (Preclinical Safety, Translational Sciences) based in Cambridge, MA. Investigative Toxicology is using non-clinical innovative investigations to discover the mechanisms of target organ toxicity and to prevent and solve pre-clinical and clinical drug safety issues. The candidate will be responsible for the design and set-up of new experimental facilities for 3 laboratories, and the management of staff therein. The candidate will also be responsible for subsequent development, implementation and management of experimental studies. The primary deliverable of these laboratories (Endocrine & Repro-toxicology, Protein & Mitochondrial Toxicology and Biochemical & Cellular Toxicology) will be to facilitate the early identification and characterisation of toxicities during preclinical phases of drug development with a particular focus on Novartis Institute for Biomedical Research (NIBR) disease areas, expertise and technologies in Cambridge. In addition, the candidate will also work closely with Preclinical Safety Project Team Representatives to help assess potential safety liabilities associated with novel drugs and their target(s). The candidate will report to the Global Head of Biochemical and Organ Toxicology and will interact closely with colleagues in other groups as a member of cross-functional and multi-disciplinary teams (including global Investigative Toxicology & Preclinical Safety departments, NIBR and external collaborators). |
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