http://www.newscientistjobs.com/jobsNew Scientist Jobshttp://www.newscientistjobs.com/jobs/job/lc-ms-product-manager-austria-austria-200643770.htmThu, 19 Nov 2009 11:44:01 +0000192104Superb opportunity for a high calibre, commercially astute scientist to “product manage” an enviable portfolio of state of the art LC/MS systems! Our client is seeking an exceptional individual with communication skills of the highest order – essential to transcend departmental boundaries. You will be responsible for accurate and up to date documentation covering sales strategies, product positioning, brochures with features/benefits and product lifecycle/future market trends. Apply now! http://www.newscientistjobs.com/jobs/job/natural-products-chemist-hertfordshire-200643630.htmThu, 19 Nov 2009 10:35:38 +0000191899You will be involved in implementing the R&D plan, designing and conducting high quality experimentation, interpreting results and contributing to the companies ideas to improve working practices and approaches. You will have a PhD or equivalent research and MUST HAVE experience of purifying and characterising natural products from bacteria, fungi or plant. You will work well in a team but also be able to take responsibility for own time management and work. Reed Specialist Recruitment Limited is an employment agency and employment business. http://www.newscientistjobs.com/jobs/job/locum-medical-scientist-biochemistry-republic-of-ireland-200642690.htmWed, 18 Nov 2009 14:18:28 +0000194350Locum Medical Scientist Biochemistry NEW ROLE JUST IN Locum Medical Scientist in Biochemistry for immediate start in busy Hospital laboratory. AMLS membership is essential. Garda clearance on file in the NRF will expedite the process significantly. Experience in a hospital biochemistry laboratory is essential as you will be required to move into the role immediately without training. For immediate consideration please apply online or contact Eamonn O'Raghallaigh on 01-6854848 http://www.newscientistjobs.com/jobs/job/team-manager-analytical-chemistry-materials-south-south-east-200639729.htmWed, 18 Nov 2009 09:06:11 +0000189229Team Manager (Analytical Chemistry/ Materials) c£25-30k South Ref: AF/015134 An experienced Team Manager in analytical chemistry (HPLC, LC/MS) with excellent people management skills is urgently required to manage an analytical team who provide a reliable testing service within R&D for a key organisation. As an analytical team manager will be responsible the management for a team who are preparing and analysing test samples using a variety of complex testing instrumentation (HPLC, GC, LC/MS/MS, ICP, GC-MS etc). You will have excellent problem solving skills to develop solutions and provide advice by applying your expertise to solve routine, non routine or novel analytical problems or challenges. Key Responsibilities • Uphold and carry out standard tests undertaken within the Materials Analysis team where there are well established and understood test methodologies. • Support the demands of the laboratory for high volume (all development products will require routine tests) and quick turnaround to produce accurate and timely results for the test requests submitted. • Develop weekly /daily activity (including testing, training, calibration, etc.) plans for team, ensuring that all appropriate options have been considered to meet customer requirements. • Implement talent management strategies to enhance the Team’s skill and flexibility to include: a) performance monitoring; b) multi-skilling; c) ‘specialist’ skills development; and seek opportunities to improve their effectiveness. • Ensure that all daily work routines are conducted in a safe manner, following defined test methods and ISO17025 protocols. Skills/ Qualifications/ Experience - Degree/ MSc/ PhD in Analytical Chemistry/ Materials background - Experience in a variety of complex instrumentation techniques HPLC, LCMSMS, GC, GC-MS, ICP etc - Relevant technical experience resulting in a thorough understanding of supervision in a high volume/quick turnaround ‘routine’ laboratory environment (ISO 17025) - Proven team management / supervisory experience to support and motivate a team in high demand situations. - Ability to understand principles of test processes/methods - Working knowledge of IT applications (Lotus Notes, Word, Excel, etc.) To Apply If you would like to be considered for this role, please contact Alison Fisher at Hudson Shribman Scientific Recruitment, quoting reference AF/015134, outlining your particular skills and experience and their relevance to this post. Please call on 020 7421 5200, or reply via email, entering the job title and reference code in the subject field to alison.fisher@hs-scientific.co.uk For up to date career opportunities please visit www.hs-scientific.co.uk Due to a high volume of applicants only shortlisted candidates will be contacted. If you are not contacted within seven days of submitting your CV please assume that your application will not be taken further. If you wish to receive feedback to obtain why your application was unsuccessful please use the contact details provided on the advert. http://www.newscientistjobs.com/jobs/job/post-doctoral-position-tawbi-laboratory-pa-pennsylvania-200638752.htmMon, 16 Nov 2009 17:07:48 +0000185735Post Doctoral Position- Tawbi Laboratory Applications are requested for a full time, postdoctoral position in the laboratory of Dr. Hussein Tawbi, Division of Hematology/Oncology, Hillman Cancer Center, University of Pittsburgh Cancer Institute. Dr. Tawbi’s laboratory studies the epigenetic regulation of DNA repair and mechanisms of post transcriptional regulation of genes associated with chemotherapy resistance. The successful applicant will be expected to have both the ability and motivation to be a major contributor to the lab’s research program. The project will involve the use of the following techniques: cell culture, RT-PCR, RNA expression, proteomics, immunohistochemistry and siRNA. These studies are primarily conducted in cell culture systems, in vivo, as well as tumor tissue, and require techniques in molecular biology and biochemistry. Candidates must hold a Ph.D in Cell Biology, or Molecular Biology. Experience with procedures on tissue culture and molecular biology methodologies are highly desirable. Excellent verbal and written communication skills are required. Dr. Hussein Tawbi M.D., M.Sc., Assistant Professor of Medicine http://www.newscientistjobs.com/jobs/job/sales-executive-southern-england-life-science-instruments-7643-united-kingdom-200638025.htmThu, 12 Nov 2009 12:32:22 +0000180122Here is a fantastic opportunity to join a leading manufacturer of life science focussed analytical instrumentation. Being the Sales Specialist - Instrumentation will involve selling the company's whole range of biotech products, including Mass Spectroscopy , DNA Analysers, Electrophoresis , and HPLC into academic, pharmaceutical and biotech accounts across the South of the UK. These are high value instruments, which means that although the company has well established accounts, the focus of your work will be on developing new business pipelines in your territory. The successful candidate will be a science graduate with strong technical knowledge of at least one aspect of analytical chemistry or biochemistry. Sales or client facing experience ( e.g applications support ) is required. You do not have to have instrument sales experience, consumables sales experience in a relevant sector would also be desirable as this would help you identify new prospective customers. You will be fully supported by the technical team. The company is experiencing strong performance despite current market conditions so please call now to find out more. A very competitive package is on offer including high OTE potential. Please call Jonathan Pearse on 01279 657716. Or email Jon@seltek.eu http://www.newscientistjobs.com/jobs/job/formulation-associate-nj-new-jersey-200628453.htmTue, 10 Nov 2009 14:39:25 +0000175999A leader in therapeutic antibodies, ImClone Systems is committed to advancing oncology care by developing a portfolio of novel targeted biologic treatments designed to address the medical needs of patients with a variety of cancers. Founded 25 years ago, ImClone Systems has a rich culture of biotechnology innovation and leading-edge medical science. Our deep expertise in molecular biology, oncology, genomics and antibody engineering has helped us establish a robust pipeline of products that are in various stages of clinical development and span virtually all major solid tumor types. The Formulation Associate will be responsible for assisting in the development of formulations for protein therapeutics, to include buffer preparation, stability studies and investigations for compatibility and delivery problems. ESSENTIAL DUTIES AND RESPONSIBILITIES 1. Operation of Spectrophotometer, pH meter, Conductivity Meter and Electrophoresis Apparatus (i.e. SDS-PAGE, IEF) 2. Operation of analytical HPLC (SEC, IEC and RP) 3. Assists in the development of analytical methods for protein analysis 4. Buffer preparation 5. Perform routine assays to test the chemical stability of proteins in relation to excipients and storage conditions 6. Data entry 7. Assay development and trouble shooting 8. Assist in the development of final drug dosage forms 9. Maintain Laboratory and Laboratory Records 10. Work in a safe manner and be compliant to ImClone Systems policies and procedures ESSENTIAL KNOWLEDGE, SKILLS, EXPERIENCE 1. BS with 2-6 years of experience, MS with 1-4 years of experience 2. Knowledge of the use of and experience with spectrophotometry, electrophoresis (SDS-PAGE and IEF), HPLC. 3. Knowledge of protein chemistry with experience in protein sample analysis and handling. 4. Knowledge and experience in buffer preparation. 5. Knowledge of and operation of biophysical analytical instrumentation will be a plus (Fluorimeter, DSC, HIAC, DLS and Osmometer). http://www.newscientistjobs.com/jobs/job/toxicology-testing-policy-advocate-london-public-sector-united-kingdom-200632183.htmThu, 05 Nov 2009 14:45:31 +0000168940Experienced Toxicologist required to provide guidance and advice on regulatory toxicology issues, specifically with a view to advancing the debate and legislation surrounding the replacement of animals in medical experiments. In this new position you will provide informed toxicological guidance and strategic input to help formulate our client’s policies on regulatory testing involving animals, engaging with regulatory authorities and a range of stakeholders throughout. This high profile role will require you to take a pro-active approach to lobbying for change with organisations such as the European Chemicals Agency (ECHA), and a wide range of interested parties involved in scientific research, ultimately influencing scientific policy involving animals in medical experiments across Europe. As Toxicology Testing Policy Advocate you’ll be supported by a professional and well-established group with an international reputation for progressing the debate on the use of animals in science. Responsibilities: • Formulate response to chemicals legislation and other toxicological testing issues • Develop and promote a strategy around REACH, promoting opportunities to further reduce animal testing • Act as key contact for the ECHA in Helsinki, attending regular meetings there and ensuring that opportunities to minimise animal testing are taken • Responding to consultations and proactively developing relationship across Europe to ensure that opportunities to reduce animal testing are maximised. • Assess opportunities to impact on animal testing by utilising REACH comment period on testing proposals, develop a strategy for response and, if necessary, provide this function looking ahead. • Provide support to Chief Executive, Policy, Ethical Standards, Legal and DMC members on issues relating to toxicity testing on animals, providing high quality scientific critiques and solutions to the problem, including keeping abreast of development with alternative methods, as require • Provide support to the Scientific Coordinator and other science consultants on toxicological and other scientific issues, as required. • Develop and maintain scientific quality control, guaranteeing high quality through peer review process of proposals and evaluation of ongoing and completed activities Skills/ Knowledge Required: • Experience of either in-vitro or in-vivo toxicological research, ideally within a regulatory context • Track record of assimilating scientific information, drafting accurate and robust scientific reports and briefings • Experience of presenting scientific information to internal and external audiences at events and meetings • Experience of successful networking with external colleagues, stakeholders and partners Employee Benefits: • 12 month interest free season ticket loan • 25 working days’ paid holiday • Employer’s Ethical Investor’s Stakeholder Pension Scheme • Generous training and professional development allowance • Flexible working hours • Childcare voucher scheme To Apply: If you would like to be considered for this role, please contact Adam Isle at Hudson Shribman Scientific Recruitment, quoting reference AI/015108, outlining your particular skills and experience and their relevance to this post. Please call on +44 (0)207 421 5232, or apply via email, entering the job title and reference code in the subject field to: adam.isle@hs-scientific.co.uk For up to date career opportunities please visit www.hs-scientific.co.uk http://www.newscientistjobs.com/jobs/job/production-chemist-isle-of-man-perm-excellent-relocation-package-isle-of-man-200628330.htmMon, 02 Nov 2009 17:04:01 +0000169026Production Chemist - Isle of Man - Perm £££excellent +relocation package NES UK are recruiting a Production Chemist for our growing Biopharmaceutical company based on the beautiful Isle of Man. The role will be working for a company which offers drug development, purification and proteomics. They now require a skilled production chemist who is has experience within a fast paced manufacturing environment. The role will involve responsibility for batch manufacture of intermediates, final ligands and chromatography resins. Carry out online QC Assays, adhere to SOP's, and carry out other duties as directed by the Production Manager. you will also be responsible for process optimisation studies on both new and existing processes, and you will participate decision making groups for process development projects Ideally you will be a degree qualified chemist and have experience in a chemistry production environment in a regulated environment. Experience in process development would be distinct advantage. This role is based on the beautiful Isle of Man and you must be prepared to relocate to the island for the role. Please apply immediately for a confidential discussion to Geoff Flavell-Matts at NES http://www.newscientistjobs.com/jobs/job/qc-chemist-x2-location-herts-hertfordshire-200628263.htmMon, 02 Nov 2009 16:23:54 +0000163815Our client is a pharmaceutical company and actively seeking a QC chemist within their analytical department. An Ideal candidate will have a degree in Pharmacy or Life Sciences with hands on experience, in using Analytical Instruments such as HPLC, UV and IR. Duties: To undertake assigned analytical testing, providing accurate results quickly and effectively. To carry out all duties in the line with the company's policies. To ensure that Good manufacturing Practice is implemented within the section, with respect to staff, and all aspects of training. Good organisation and communication skills. Candidates must be eligible to live and work in the UK. http://www.newscientistjobs.com/jobs/job/scientist-ii-chemistry-ma-massachusetts-200618871.htmThu, 22 Oct 2009 16:10:01 +0000147138This position will be responsible for developing methods of analysis in order to understand and characterize polysaccharide serotypes derived from new production and purification processes. - Experience in the area of glycobiology highly desired but not necessary; - Experience with analytical techniques such as U/HPLC, HPSEC-MALS, GC-MS, and gel electrophoresis; - Take an active role, together with the supervisor and project team, in the planning and execution of experiments; - Good presentation and writing skills; - Responsible for all laboratory aspects of the project, including setting up instruments, performing experiments, and collecting and analyzing data; - Organize and report results in a timely manner; - Participate in project team meetings by presenting and discussing results; - Work closely with supervisor and project members by providing input into the decision-making process; - Responsible for long-term and day-to-day planning actives; - Interested in continuous improvement and learning new laboratory techniques; - Help cross-functional areas solve technical problems; Qualifications: A Master's Degree in a field of science with a minimum of 2 years relevant academic or pharmaceutical laboratory experience or a Bachelor's Degree with a minimum of 4 years relevant laboratory experience. Throughout our 153 years, a legacy of caring for others has been at the heart of everything we do at Pfizer. This commitment is no less important when it comes to our employees. Pfizer wants to ensure that employees have resources to help them develop and succeed both in their careers and personal lives. One way we can achieve this is through our comprehensive benefits program, which offers employees and their eligible dependents the variety and flexibility to help address their needs at different stages in life. Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. All applicants must have authorization to work for Pfizer in the U.S. In certain circumstances it may be advantageous to Pfizer to support the application(s) for temporary visa classification and/or sponsor applications for permanent residence so that a foreign national colleague can accept or remain in a work assignment in the U. S. For certain classes of temporary visa, the resulting work authorization may be specific to Pfizer and the specific job and/or work site. Pfizer may at its business discretion decide to or refrain from obtaining, maintaining and/or extending the temporary visa status and/or sponsoring a colleague for permanent residence and /or employment eligibility, considering factors such as availability of qualified U.S. workers and the colleague's long-term prospects for securing lawful permanent residence, among other reasons. Employment applicants requiring immigration sponsorship must disclose, when initial application for employment is made, whether or not they are legally authorized to work for Pfizer in the U.S. and, if so, whether that authorization permits them to work in the job they seek. In no case should Pfizer's support of a colleague's temporary visa application or sponsorship of a colleague for permanent residence be construed to guarantee success of that application or amend or otherwise invalidate the "at-will" employment relationship between the colleague and Pfizer. HOW TO APPLY: Please copy and paste the following URL into your browser address bar: http://posttrak.arbita.net/cgi-bin/PostTrak.cgi?RefCode=R9257125807854 http://www.newscientistjobs.com/jobs/job/director-of-research-multiple-openings-china-200617935.htmThu, 22 Oct 2009 09:02:27 +0000146991Due to recent expansion and internal growth, Kemin Industries has multiple R&D Director positions available. These positions are located in China, Belgium and U.S.A. Kemin Industries, Inc., is a privately held global life science company headquartered in Des Moines, Iowa, with a vision to “improve the quality of life by touching half the people of the world every day with our products and services.” Kemin develops nutritional solutions that serve a variety of industries ranging from Agrifoods to Pharmaceuticals. These positions are responsible for research and development of products from conception to commercialization in their respective markets. The positions require extensive management experience, including budgeting and management of a wide array of projects and research teams. Excellent interpersonal and communications skills are required in these hands-on roles. Domestic and international travel is likely. Director, Research & Development - Kemin AgriFoods (Europe and China) Ph.D. in Animal Science, Biochemistry, Organic Chemistry or Microbiology; At least 7 years of broad scientific/ag-oriented experience and knowledge base (chemistry, biochemistry, animal feed/nutrition, microbiology, agronomy, statistical analysis, technical writing, practical field experience, etc.); A proven track record of accomplishment in product commercialization. Director, Research & Development - Kemin Health (U.S.A.) Ph.D. in biochemistry, microbiology, organic chemistry or comparable discipline; At least 7 years of experience in the nutraceutical and/or vitamin and dietary supplement industries is preferred with a proven track record of identifying and developing new technologies resulting in successful product commercialization. Director, Research & Development, Regulatory Affairs - Kemin Nutrisurance (U.S.A.) Ph.D. in biochemistry, organic chemistry or comparable discipline; At least 7 years experience in the pet food and/or animal health and/or animal agriculture industries is preferred with a proven track record of identifying and developing new technologies resulting in successful product commercialization. A solid Regulatory Affairs understanding is also required. More information about Kemin, its products and industries served can be found at www.kemin.com. Please submit resume, cover letter, and salary expectations to: jobs@kemin.com or Kemin Human Resources, 2100 Maury Street - PO Box 70, Des Moines, Iowa 50306-0070. Kemin is an equal opportunity employer http://www.newscientistjobs.com/jobs/job/senior-research-scientist-i-ny-new-york-200616756.htmTue, 20 Oct 2009 14:59:21 +0000145457Responsibilities: • Proposes, plans and conducts research projects including complex experiments, some in parallel, utilizing current concepts and recognized standard techniques, developing new protocols as necessary. Demonstrates advanced level of problem solving and troubleshooting. • Demonstrates a high level of initiative in performing experiments, analyzing data and drawing conclusions regarding progress and results of work. Routinely designs experimental procedures, and implements new procedures with minimal supervision. Summarizes research in regular reports and communicates results of research to supervisor and in team meetings. • Gathers and records laboratory observations and data, records information lab notebooks and databases and documents experimental design and changes to protocol. Duties are performed with an understanding of drug discovery in area of specialization. Analyzes data, performs calculations and draws final conclusions regarding progress and results of work. • Quickly learns and accurately performs new procedures involving a range of technologies. Maintains a familiarity with current and emerging technologies through reading and understanding scientific and technical literature resulting in a broadening understanding of disciplines outside area of training and enabling the use of new and improved procedures in the laboratory. • Begins to set goals for projects and assigns priorities to individual experiments. Assists in the maintenance of laboratory function, keeping lab clean and working in accordance with good safety practices. • Demonstrates scientific curiosity through reading and talking with colleagues and begins to apply knowledge toward a broader understanding of therapeutic area and drug discovery process. • Required to present at section meetings and write reports for internal communications and makes significant contributions to the preparation of papers for peer review journals and/or patents. Qualifications: Ph.D. in a field of science with a minimum of 0-1 year experience. Typical relevant degree disciplines include Biochemistry, Biology, Analytical Chemistry, Synthetic Organic Chemistry, Clinical Pathology, Clinical Pharmacy, Clinical Projects, Molecular Biology, Pharmacy, Pharmacology, Regulatory Release, Toxicology, Microbiology and Biopharmacy. Throughout our 153 years, a legacy of caring for others has been at the heart of everything we do at Pfizer. This commitment is no less important when it comes to our employees. Pfizer wants to ensure that employees have resources to help them develop and succeed both in their careers and personal lives. One way we can achieve this is through our comprehensive benefits program, which offers employees and their eligible dependents the variety and flexibility to help address their needs at different stages in life. Pfizer Inc: Working together for a healthier world™ Founded in 1849, Pfizer is the world's premier biopharmaceutical company taking new approaches to better health. We discover, develop, manufacture and deliver quality, safe and effective prescription medicines to treat and help prevent disease for both people and animals. We also partner with healthcare providers, governments and local communities around the world to expand access to our medicines and to provide better quality health care and health system support. At Pfizer, colleagues in more than 90 countries work every day to help people stay happier and healthier longer and to reduce the human and economic burden of disease worldwide. HOW TO APPLY: Please copy and paste the following URL into your browser address bar: http://posttrak.arbita.net/cgi-bin/PostTrak.cgi?RefCode=R8583125807855 http://www.newscientistjobs.com/jobs/job/sample-information-coordinator-yorkshire-200614576.htmSat, 17 Oct 2009 14:16:01 +0000143056As a Sample Information Co-ordinator, you are responsible for co-ordinating the accuracy of all sample related information which is entered into the Laboratory Information Management System (LIMS). You are responsible for ensuring that information and sample labels are maintained and corrected as necessary throughout the course of each study. Checking the sample paperwork provided by Sample Management is accurate, complete and stored in appropriate Bioanalytical files. You are required to monitor the sample logging process to ensure that the required timelines for analysis are met. You will respond to and resolve sample management queries in relation to shipments and samples. You will also be responsible reconciling samples in LIMS. http://www.newscientistjobs.com/jobs/job/experimental-officer-3-in-bioanalytical-services-yorkshire-200614535.htmSat, 17 Oct 2009 08:09:58 +0000143051As an Experimental Officer, you will provide operational support necessary for the performance of studies carried out in the Bioanalytical Services Department. You will provide support for screening studies and will participate in a wide range of analytical techniques and procedures, working with minimal supervision. You will work closely with scientists (Study Managers/Technical Experts) to ensure studies are performed according to appropriate scientific and technical standards and in a timely, cost effective manner. You will be involved with the day to day aspects of screening including instrument set-up, assay development, sample analysis, data processing and data reporting. http://www.newscientistjobs.com/jobs/job/postdoctoral-associate-microfluidics-specialist-va-virginia-200611265.htmFri, 16 Oct 2009 13:40:19 +0000141647The Virginia Bioinformatics Institute (VBI) is a research institute dedicated to the study of the biological sciences. By using bioinformatics, which combines transdisciplinary approaches to information technology and biology, researchers at VBI interpret and apply vast amounts of biological data generated from basic research to some of today's key challenges in the biomedical sciences. VBI develops genomic, proteomic and bioinformatics tools that can be applied to the study of infectious diseases as well as the discovery of new vaccines, drugs and diagnostic targets. VBI strongly emphasizes synergistic interactions among faculty and is organized around the concept of team science. The Microfluidics group at VBI, aimed at developing fully integrated, stand-alone microfluidic devices with mass spectrometry detection for high-throughput proteomic investigations, currently seeks a Postdoctoral Associate for Microfluidics and Mass Spectrometry research. The Postdoctoral Associate will work as part of a team of scientists and researchers who design and evaluate the performance of microfluidic devices. The Postdoctoral Associate will be responsible for developing multidimensional separations with mass spectrometry detection on the chip, and for performing microfluidic flow modeling. The chips will be used for the analysis of cellular extracts and biomarker discovery/screening applications. Required Qualifications: -Ph.D. in Chemistry or Engineering or related field. -Demonstrated experience with microfluidic chip operation. -Experience using commercial software for modeling microfluidic flows. -Ability to work independently as well as with research group. -Good communication skills, strong work habits and motivation. Preferred Qualifications: -Experience with bioanalytical instrumentation. Interested candidates should submit a letter of interest and CV upon by clicking Apply Now below and searching by posting number 090377. Review of applications will begin for this position on July 22, 2009. Compensation commensurate with experience. To learn more about VBI, please visit our website. An Equal Opportunity/Affirmative Action Institute http://www.newscientistjobs.com/jobs/job/computational-chemistry-and-biology-opportunities-at-d-e-shaw-research-ny-new-york-200396722.htmThu, 15 Oct 2009 15:29:19 +0000140445Computational Chemistry and Biology Opportunities at D. E. Shaw Research Extraordinarily gifted computational chemists, biologists, and other computational scientists are sought to join a rapidly growing New York–based research group that is pursuing an ambitious, long-term strategy aimed at fundamentally transforming the process of drug discovery. Candidates should have world-class credentials in computational chemistry, biology, or physics, or in a relevant area of computer science or applied mathematics, and must have unusually strong research skills. Relevant areas of experience might include protein structure prediction, the computation of protein-ligand binding affinities, the study of biologically important systems using molecular dynamics and/or Monte Carlo simulation, and the application of statistical mechanics to biomolecular systems—but specific knowledge of any of these areas is less critical than exceptional intellectual ability and a demonstrated track record of achievement. Current areas of interest within the group include molecular dynamics simulation of functionally significant globular and membrane proteins, the prediction of protein structures and binding free energies, structure- and ligand-based drug design, characterization of protein-protein, protein-nucleic acid and protein-lipid interactions, and the development of algorithms for biomolecular simulations. This research effort is being financed by the D. E. Shaw group, a global investment and technology development firm with more than US $30 billion in aggregate investment capital. The project was initiated by the firm's founder, Dr. David E. Shaw, and operates under Dr. Shaw's direct scientific leadership. We are eager to add both senior- and junior-level members to our world-class team, and are prepared to offer above-market compensation to candidates of truly exceptional ability. Please send your curriculum vitae (including list of publications, thesis topic, and advisor, if applicable) by clicking Apply Now. D. E. Shaw Research does not discriminate in employment matters on the basis of race, color, religion, gender, pregnancy, national origin, age, military service eligibility, veteran status, sexual orientation, marital status, disability, or any other protected class http://www.newscientistjobs.com/jobs/job/project-manager-pharmaceutical-south-united-kingdom-200610966.htmWed, 14 Oct 2009 11:42:11 +0000139405Project Manager (Pharmaceutical) c£30-45k South Ref: AF/015027 An opportunity has arisen for an experienced project manager to act as a liaison between the client and organisation to ensure that all needs are met concerning both project budgets and timelines. Main Job Responsibilities: • Manage an appropriate number of active projects for pre-formulation onwards for major clients. • Lead project meetings, teleconferences, face-to-face interactions, including the generation of team minutes. • Generation, updating and facilitating agreement to project plans, including the accuracy of revenue forecasting, data transfer to the Sales Order Register (SOR), and timely invoicing to clients on completion of project milestones. • Manage the generation, monitoring and control of assigned project Timesheets, ensuring full transparency of performance versus budget for all assigned projects, within the project teams, and with the Senior Management team. • Resolves project issues and resource constraints within the team • Facilitate positive team member interactions and manage conflict • Manage client satisfaction by managing client expectations efficiently. Proven ability to keep client relationships on track and ability to mend difficult relationships. • Responsible for timely preparation, negotiation and approval of all Changes of Scope, involving the relevant business manager(s) where appropriate Qualifications, Skills and Experience Background: Chemistry/ Pharmacy/ Biological Sciences Pharmaceutical Development, Clinical trials Manufacture, Commercial Manufacture, Project Management, Financial awareness, Client contact Excellent organisational skills Ability to communicate at all levels To Apply If you would like to be considered for this role, please contact Alison Fisher at Hudson Shribman Scientific Recruitment, quoting reference AF/015027, outlining your particular skills and experience and their relevance to this post. Please call on 020 7421 5200, or reply via email, entering the job title and reference code in the subject field to alison.fisher@hs-scientific.co.uk For up to date career opportunities please visit www.hs-scientific.co.uk Due to a high volume of applicants only shortlisted candidates will be contacted. If you are not contacted within seven days of submitting your CV please assume that your application will not be taken further. If you wish to receive feedback to obtain why your application was unsuccessful please use the contact details provided on the advert. http://www.newscientistjobs.com/jobs/job/postdoctoral-fellow-biochemist-opth207-wv-west-virginia-200605523.htmThu, 08 Oct 2009 16:57:45 +0000174395Postdoctoral Fellow (OPTH207) The West Virginia University Research Corporation (WVURC) seeks to hire a Postdoctoral Fellow to participate in the NIH-funded studies of chaperonin-dependent protein folding in neurons. The multidisciplinary nature of these studies provides an opportunity to acquire hands-on training in the transgenic models, microarrays, proteomics and fluorescent microscopy. A competitive NIH salary scale and benefits package will be offered. The position is located in Morgantown, WV, a tightly-knit college town surrounded by the beautiful Appalachian nature. Required qualifications: a recent PhD in molecular biology, biochemistry or related discipline; 2-4 years of experience utilizing modern biochemistry/molecular biology approaches in a research lab; proficiency in verbal and written English; keen interest and commitment to the research; and experience with lab animals. Visit http://www.hsc.wvu.edu/som/bmp/sokolov.asp for more information about the lab. In order to receive consideration for this position, applicants must apply online (URL can be found below by clicking View Contact Details). AA/EOE/E-Verify compliant employer. http://www.newscientistjobs.com/jobs/job/postdoctoral-fellow-united-states-200593993.htmTue, 06 Oct 2009 16:14:50 +0000138656POSTDOCTORAL FELLOW position is available immediately to join the collaborative research group of Dr. Jeffrey D. Cirillo studying tuberculosis pathogenesis. Selected individual will be primarily responsible for conducting independent research on mycobacterial pathogens and publication of results. Research will emphasize the molecular, biochemical, cell biological, live-animal molecular imaging and immunological characterization of virulence determinants in mycobacteria and their interactions with the host in mice and guinea pig virulence models. Ph.D. required and a record of productive experience in molecular biology of bacterial pathogens preferred. Send curriculum vitae and names and addresses of three references postmarked by November 15, 2009 (or until a suitable candidate is found), to Dr. Jeffrey D. Cirillo, Dept. Microbial & Molecular Pathogenesis, (please find full mailing address below by clicking View Contact Details as well as Fax and Website URL) Texas A&M University System Health Science Center is an affirmative action/equal opportunity employer. Contact: Dr. Cirillo, Telephone: 979-458-0778 for additional information.