http://www.newscientistjobs.com/jobsNew Scientist Jobshttp://www.newscientistjobs.com/jobs/job/process-continuous-improvement-scientist-south-fuel-cells-united-kingdom-200625004.htmThu, 29 Oct 2009 14:56:42 +0000158444As a continuous improvement scientist you will provide technical expertise and understanding to the continuous improvement group. You will help deliver effective Membrane Electrode Assembly (MEA) manufacturing for our client’s Fuel Cell components, integrating existing processes and developing new methods. You will be technically focussed, but committed to delivering the business’ needs and supporting your group to complete product and process trials to deadlines. Main Responsibilities: Drive the process trials to ensure that business needs are met Analyse the capability of current and new MEA manufacturing methods Provide optimum MEA functionality, using analysis of physical and electrochemical properties Prepare and analyse MEA sections using optical microscopy, Scanning Electron Microscopy (SEM), and Transmission Electron Microscopy (TEM) Draft operating procedures, identifying process set points and operating windows Communicate trial results with all levels of staff in the trial group Essential Skills/ Experience: Proven practical experience of implementing process or product improvement programmes to deadlines within a science/ engineering environment Materials Science / Chemistry qualification or related discipline Materials analysis skills (SEM/ TEM) Desirable Skills/ Experience: Understanding and knowledge of the Fuel Cell sector/ manufacturing process Benefits: This is a permanent job with a fantastic employer offering a great benefits package in addition to the basic salary: Pension Scheme - Hybrid scheme combining Defined Contribution and Defined Benefit scheme in combination with the State Second Pension; 25 Days Holiday; Share Incentive Plan – after 1 year; Incentive Bonus- after a qualifying period of 3 months; Long Service Awards; Subsidised Restaurant & Refreshments; Child Care Vouchers; Christmas Gift; Free Parking To Apply: If you would like to be considered for this role, please contact Adam Isle at Hudson Shribman Scientific Recruitment, quoting reference AI/015082, 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/managersenior-manager-operations-bst-accounting-md-maryland-50001667.htmTue, 27 Oct 2009 14:56:05 +0000153575My company shares my passion for helping to improve human health around the world.” “This is My MedImmune.” Those who join MedImmune feel a sense of ownership about their future. They thrive with a recognized leader in the biotechnology industry and the wholly-owned subsidiary of AstraZeneca plc. Here, you will join passionate professionals who advance science, technology and medicine to develop products designed to help people live better lives. You will excel in an environment characterized by respect, integrity and growth opportunities…that encourages both individual contribution and collaborative entrepreneurial thinking. Our products and/or product candidates are designed to address areas of need in infection, oncology, respiratory disease and inflammation, cardiovascular/gastrointestinal disease and neuroscience. Explore a MedImmune career as we strive to better more lives, more often, around the world. Title: Manager/Senior Manager, Operations BST Accounting Location: MD, Gaithersburg - Corporate Headquarters Req: 02057 Position Summary: This position is responsible for managing the Accounting function within the Operations BST, including the monthly financial close process and related reporting activities, and the monthly consolidation of foreign subsidiaries. The incumbent is a key interface between the Finance Operations BST in Gaithersburg, colleagues in Finance Operations BST at remote supply sites and the Corporate Controller’s team. This position leads a team responsible for accounting for intercompany transactions among related entities, both in the US and abroad. This position will also be expected to provide financial support, in terms of forecasting and analysis of actual results, for assigned functions within MedImmune’s Operations group. The incumbent will be expected to participate in and support strategic and process improvement initiatives within Operations and Finance. Major Duties and Responsibilities (including supervising others): • Provides leadership and coordination of the monthly close process for Finance Operations BST. • Manages the process of accounting for intercompany transactions between MedImmune and its foreign operations in the UK and the Netherlands. • Responsible for updating monthly foreign exchange rates and executing the monthly consolidation of foreign entities, and understanding the key drivers behind associated foreign exchanges gains and losses. • Manages the process of calculating appropriate transfer pricing and accounting for intercompany transactions between the various legal entities involved in the MedImmune US supply chain (MEDI, MEDL, MECO). • Provides updated financial forecasts by legal entity to the AstraZeneca tax department each quarter for use in projecting annual tax expenses. • Responsible for ensuring monthly Royalty Expense is recorded correctly and, further, ensuring all Royalty payments are made on time and pursuant to terms of the individual agreements. Also provides support, as needed, to audits on any of the associated agreements. • Responsible for estimating annual Royalty Expenses to be included in all financial forecasts (ABU, RBU, LROP). • Coordinates collection, compilation and submission of Operations related commentary in support of the monthly close meeting and the monthly Management Review meeting. • Provides business partnering and financial analysis/forecasting support to assigned areas of Operations. • Ensures all of the work outlined in points above is completed pursuant to standards established by MedImmune Company policy, including Sarbanes-Oxley compliance. JOB REQUIREMENTS: Requirements/Qualifications: Education: BS/BA in Accounting or related field required MBA preferred CPA strongly preferred Experience: 5-7 years progressive experience in Accounting and/or Finance roles Experience with a global company required, with manufacturing background preferred. Experience with foreign consolidation required (IAS 21, IAS 27, FAS 52, ARB 51). Direct supervisory and management experience required. Special Skills/Abilities: Job Complexity: Supervision: (Supervision required, level of independence If you are interested in this position please click the Apply Now button below and search for Req #. 02057. MedImmune is an Equal Opportunity Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, veteran status, or any other characteristic protected by federal, state or local law. http://www.newscientistjobs.com/jobs/job/customer-support-engineer-south-fuel-cell-company-united-kingdom-50001636.htmTue, 27 Oct 2009 12:36:28 +0000153526As Customer Support Engineer you will provide technical support to customers and the Sales & Marketing team, help communicate customer issues and requirements and drive customer service standards and objectives to a successful conclusion. You will also help provide insights to support the development or new and existing products. Our client is a leading Fuel Cell company, and as Customer Support Engineer you will be joining a team which works across both technical (scientific and engineering) and business support (sales and marketing, customer services) functions, so your communication skills and ability to understand and concisely deliver technical information will be key to your success. Main Responsibilities: Provide effective technical support to customers in their use of our client’s products Drive customer projects to conclusion within an agreed timeframe Assist in ensuring product qualification is achieved in a timely manner, in line with plan Communicate customer issues and requirements to the key stakeholders within the business Actively participate in the gathering and reporting of accurate and up-to-date market intelligence Required Experience: Proven track record managing projects both internally and with customers Be able to demonstrate a knowledge and understanding of fuel cells Proven track record of being able to influence at all levels and work effectively across departments Able to work with and challenge the “experts” Good presentation skills A degree or equivalent experience in a relevant scientific or engineering discipline Previous work experience with Fuel Cells/ Membrane Electrode Assemblies (MEAs) desirable Benefits: This is a permanent job with a fantastic employer offering a great benefits package in addition to the basic salary: Pension Scheme; 25 Days Holiday; Christmas Gift; Share Incentive Plan (after 1 year) & Incentive Bonus (after 3 months); Long Service Awards; Subsidised Restaurant & Refreshments; Child Care Vouchers; Free Parking. To Apply: If you would like to be considered for this role, please contact Adam Isle at Hudson Shribman Scientific Recruitment, quoting reference AI/015074, 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/senior-project-control-analyst-md-maryland-200620240.htmFri, 23 Oct 2009 19:13:41 +0000149786My company shares my passion for helping to improve human health around the world.” “This is My MedImmune.” Those who join MedImmune feel a sense of ownership about their future. They thrive with a recognized leader in the biotechnology industry and the wholly-owned subsidiary of AstraZeneca plc. Here, you will join passionate professionals who advance science, technology and medicine to develop products designed to help people live better lives. You will excel in an environment characterized by respect, integrity and growth opportunities…that encourages both individual contribution and collaborative entrepreneurial thinking. Our products and/or product candidates are designed to address areas of need in infection, oncology, respiratory disease and inflammation, cardiovascular/gastrointestinal disease and neuroscience. Explore a MedImmune career as we strive to better more lives, more often, around the world. Title: Senior Project Control Analyst Location: MD, Gaithersburg - Corporate Headquarters Req: 01975 Position Summary: Major Duties and Responsibilities: Works closely and directly with Project Management, Sourcing, and Engineering teams Maintains EAC and monthly updates to project financial performance Presents monthly financial status, including graphics Approves POs and other requests against ETC budget Reviews all cost activity for allowability prior to payment Approves all subcontractor invoices prior to payment Leads pricing activity Cradle to Grave execution Special Skills/Abilities: Project Controls, Scheduling, MS Project, Resource Loaded Networks (RLNs), Work Breakdown Structures (WBS). Job Complexity: Requires high level of analytical skills, significant manual process, substantial work with other organizations. Supervision: Can work independently, self-starter, can complete efforts with little guidance. (Supervision required, level of independence) JOB REQUIREMENTS: Requirements/Qualifications: Education: Prefer BS in Accounting for Finance, will consider non-degreed with significant project control experience. Experience: 5-10 years experience, preferably 3+ years in project control, preferably with a gov¡¦t contractor. Special Skills/Abilities: Project Controls, Scheduling, MS Project, Resource Loaded Networks (RLNs), Work Breakdown Structures (WBS). If you are interested in this position please click the Apply Now button below and search for Req # 1975. MedImmune is an Equal Opportunity Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, veteran status, or any other characteristic protected by federal, state or local law. http://www.newscientistjobs.com/jobs/job/mechanicalhvac-engineer-md-maryland-200620236.htmFri, 23 Oct 2009 19:09:23 +0000149782My company shares my passion for helping to improve human health around the world.” “This is My MedImmune.” Those who join MedImmune feel a sense of ownership about their future. They thrive with a recognized leader in the biotechnology industry and the wholly-owned subsidiary of AstraZeneca plc. Here, you will join passionate professionals who advance science, technology and medicine to develop products designed to help people live better lives. You will excel in an environment characterized by respect, integrity and growth opportunities…that encourages both individual contribution and collaborative entrepreneurial thinking. Our products and/or product candidates are designed to address areas of need in infection, oncology, respiratory disease and inflammation, cardiovascular/gastrointestinal disease and neuroscience. Explore a MedImmune career as we strive to better more lives, more often, around the world. Title: Mechanical/HVAC Engineer Location: MD, Gaithersburg - Corporate Headquarters Req: 02054 Position Summary: HVAC/Mechanical Engineer specialist for the Engineering Technical Support function supporting MedImmune sites globally. Independently applies advanced and diverse engineering principles to the design, implementation, startup and commissioning of major HVAC & mechanical system modifications, processes and/or capital projects and/or troubleshooting of operational issues in operations, manufacturing, laboratories and pilot plants. Develops, organizes, analyzes and presents interpretation of results for operational issues or engineering projects of significant scope and complexity. Major Duties and Responsibilities (including supervising others): Provide technical solutions to a wide range of difficult problems involving mechanical services. Solutions are imaginative, thorough, practicable, and consistent with organization objectives. Provide guidance and supervision to the interpretation of project objectives and application of standards in the design and operation of mechanical services for manufacturing, laboratory and administrative facilities. Advise on the alternate methods of construction and direct architects and consulting engineers in the execution of engineering solutions for various projects. Work collaboratively with capital project teams, site engineering teams, and site operations in the application of engineering solutions on capital projects. Provide site-to-site knowledge transfer to promote consistency across MedImmune. Support engineering design (Basis of Design, Conceptual Design, Schematic Design and Detailed Design), create and maintain specifications, standards, and design guidelines as well as support continuous improvement initiatives (i.e. Lessons Learned). Coordinate the work of consultants, architects and engineering firms on development of standard design documents. Develop strategies and recommendations for HVAC/mechanical services as well as work with the Project Controls Group to estimate the cost of recommended improvements and/or upgrades. Prepare and defend recommendations using fact-based justification; life cycle cost analysis experience is required. Exercise considerable latitude in determining technical objectives of assignment. Review completed work from a relatively long- term perspective, for desired results. Supervision and guidance relate largely to overall objectives, critical issues, new concepts, and policy matters. Broader job responsibilities include: • Complete complex or novel assignments requiring development of new and/or improved engineering techniques and procedures • Develop engineering policies and procedures that affect multiple organizational units • Employ advanced engineering techniques and/or modifications of advanced techniques within area of engineering expertise • Apply knowledge of engineering principles and practices outside of area of discipline expertise to broad variety of assignments in related fields • Develop technical solutions to complex problems requiring the regular use of ingenuity and creativity • Work with research, manufacturing, distribution, process development, utilities, facilities, quality assurance and risk management departments in developing requirements and recommendations for large and/or highly complex system/facility modifications • Work with project managers to complete design and engineering projects within schedule, budget and quality constraints • Guide the successful completion of major programs and may function in a project leadership role • Represent the organization as the prime technical contact on contracts and projects; interact with senior external personnel on significant technical matters often requiring coordination between organizations • The job will require periodic travel both domestically and internationally. Knowledge, skills and abilities: JOB REQUIREMENTS: • Bachelor’s degree in Mechanical Engineering, or related field or equivalent combination of education and experience • Typically 12+ years of relevant work experience 9+ years experience in biotech pharmaceutical industry • Established expertise in engineering technology of mechanical services for the biotech pharmaceutical industry, including experience with sterile systems, hygienic piping, and clean rooms • Experience with applicable codes is required; additional experience with codes and requirements in Europe preferred • Direct experience with regulated environments (i.e. cGMP, OSHA, EPA) is also required • Practical start-up and commissioning experience • Business process modeling experience preferred Required Skills: • Ability to independently determine when additional external resources are required to solve problems • Ability to provide solutions to a large variety of technical problems of moderate to large complexity and scope • Problem solving skills requiring the application of scientific and engineering theory and calculations and creative skills in the development of hypotheses and approach. • Working knowledge of financial analysis tools • Ability to delegate and manage the project work of others • Demonstrated skills in the following areas: o Negotiation, persuasion and facilitation o Collaboration o Project cost development o Conflict resolution o Leadership and teambuilding o Management of contractors and vendors If you are interested in this position please click the Apply Now button below and search for Req #. 02054. MedImmune is an Equal Opportunity Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, veteran status, or any other characteristic protected by federal, state or local law. http://www.newscientistjobs.com/jobs/job/director-building-systems-md-maryland-200620233.htmFri, 23 Oct 2009 19:06:54 +0000149781My company shares my passion for helping to improve human health around the world.” “This is My MedImmune.” Those who join MedImmune feel a sense of ownership about their future. They thrive with a recognized leader in the biotechnology industry and the wholly-owned subsidiary of AstraZeneca plc. Here, you will join passionate professionals who advance science, technology and medicine to develop products designed to help people live better lives. You will excel in an environment characterized by respect, integrity and growth opportunities…that encourages both individual contribution and collaborative entrepreneurial thinking. Our products and/or product candidates are designed to address areas of need in infection, oncology, respiratory disease and inflammation, cardiovascular/gastrointestinal disease and neuroscience. Explore a MedImmune career as we strive to better more lives, more often, around the world. Title: Director, Building Systems Location: MD, Gaithersburg - Corporate Headquarters Req: 02053 Position Summary: Major Duties and Responsibilities (including supervising others): The Director, Building Systems is a recognized expert in the field leading an Engineering group within Global Engineering and Facilities that is responsible for acting as the interface between MedImmune¡¦s internal scientific, development, manufacturing, project management resources and our key outside Engineering providers in the specialty area of Building Systems. This function is not chartered to develop new building and utility systems per se as this is a design function, but would be expected to support translation of user requirements and business case relevancies to projects specifically through basis of design and construction drawing stages. With a strong focus on Laboratory/Infrastructure projects in the upcoming capital plan, the individual will be expected to develop and maintain strong relationships with business leaders in these two project types. The group requires a technical proficiency to answer technical needs as necessary and would be expected to be familiar with design processes in varied regions of the world, under varying regulatory requirements for the following potential disciplines: HVAC Geotechnical Utility Systems Electrical Piping Hygienic and non-hygienic Fire Protection Structural Telecommunication/Security Civil Material Handling Architectural Interior Design The group will develop and maintain building system design standards, guides, process, and procedures that codify MedImmune¡¦s required practices. It is expected that this group help develop and coordinate MedImmune¡¦s approaches to all systems noted above in this regard including the document retention, version and storage of CADD drawings. In addition to the technical role, there is an expectation that this individual develop and maintain resourcing tools to be able to understand the required disciplines required to service the projects and be able to acquire and manage both FTE¡¦s and contract staff. Other department-wide metric development and monitoring will be the responsibility of this role. Leadership skills are essential. The leader of this function and the group itself would be expected to be a key company interface with outside Engineering firms. While those firms routinely execute the design of various building system engineering documents necessary to enable a capital project. MedImmune¡¦s Building Systems group acts as the bridging function between the outside firm¡¦s technical staff and MedImmune internal groups (Development, Research, Manufacturing, EH&S, Quality) that are responsible for MedImmune¡¦s R&D or manufacturing technology. Leading across the many organizational functions will be a key attribute required. As such the group manages the process of delivering design services within the Capital and Life Cycle Management system. Knowledge, skills and abilities: Must possess in-depth technical and operational knowledge of unit operations used in biotechnology manufacturing including bioreactor cell culture, ultrafiltration, centrifugation, and chromatography and then translate those into the designs for utility and support systems. Demonstrated project management, technology transfer, problem-solving, and team leadership abilities are required. Thorough knowledge of current GMP regulations and an understanding of global regulatory agency expectations and current industry practices in process and utility operations. Must understand the process of how MedImmune¡¦s internal business process and technical knowledge is used by our outside Engineering firms to drive their own internal project execution processes. Must have a strong sense of what the strengths/weaknesses and proper role of the outside Engineering firms are as they execute MedImmune capital projects. Must be flexible and able to effectively manage multiple projects and priorities. Good interpersonal skills are required, as is the ability to communicate well, both verbally and written. The individual in this position is expected to represent MedImmune interests, objectives and policies in a professional and responsible manner. JOB REQUIREMENTS: Requirements/Qualifications: Education: B.S. or M.S. degree in Mechanical, Chemical, Civil, Electrical, or Biochemical Engineering or in a relevant engineering discipline. Experience: twenty years relevant experience in a commercial biopharmaceutical manufacturing and R&D environment is required, with at least five years managing a building systems engineering group or likeness thereof. Experience also with the building service engineering function of one or more of the large engineering services firms routinely serving the BioPharmaceutical industry would be considered a strong plus. Special Skills/Abilities: Team based training, total quality training, Job Complexity: Supervision: Reports to Senior Director, Engineering Technical Support. The role will supervise 6 +/- senior technical people, both regular full-time and contract. The role will routinely interface with project managers and senior internal scientists and personnel in Development, Research and Manufacturing Sciences. If you are interested in this position please click the Apply Now button below and search for Req #. 02053. MedImmune is an Equal Opportunity Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, veteran status, or any other characteristic protected by federal, state or local law. http://www.newscientistjobs.com/jobs/job/quality-systems-engineer-iv-md-maryland-200619802.htmFri, 23 Oct 2009 15:29:59 +0000149728My company shares my passion for helping to improve human health around the world.” “This is My MedImmune.” Those who join MedImmune feel a sense of ownership about their future. They thrive with a recognized leader in the biotechnology industry and the wholly-owned subsidiary of AstraZeneca plc. Here, you will join passionate professionals who advance science, technology and medicine to develop products designed to help people live better lives. You will excel in an environment characterized by respect, integrity and growth opportunities…that encourages both individual contribution and collaborative entrepreneurial thinking. Our products and/or product candidates are designed to address areas of need in infection, oncology, respiratory disease and inflammation, cardiovascular/gastrointestinal disease and neuroscience. Explore a MedImmune career as we strive to better more lives, more often, around the world. Title: Operations Analyst I Location: MD, Gaithersburg - Corporate Headquarters Req: 02043 Primary responsibilities will include participating in special projects to effectively assist the Medical Organization with key decision support in managing the business operations, oversight of the Medical Organization invoice process, tracking, reporting and training of other Medical Organization personnel on invoice processing, and coordinating as necessary, in the business plan and evaluation of risks and opportunities with upper management, resourcing analysis, InSight reporting and resource planning maintenance and updates. Duties include coordination and management of the Medical Organization invoice review and approval process. Develop and provide department heads and clinical operations team with detailed reporting to assist in the management of outstanding invoices and disputes. Involve in all aspects of the invoice process for the Medical Organization, including the review and update of the work process documents, process improvement initiatives and maintenance of the central MedOrg Invoices helpdesk email box. Perform ad hoc analyses, as required with general supervision from Manager, Medical Operations. Participate in the development of business models and metrics for the Medical Organization and will eventually assist in the consolidation of the Performance Metrics Summary for upper management. This position will work on simple to complex problems where the ability to assess and analyze situations, to adapt to the changing environment of the business, and to create efficiencies in managing the process are fundamental. With general supervision from the Manager, Medical Operations, this position will lend support to the overall business operations activities managed and directed within the Resource Performance Management group, in addition to the various cross-functional teams within the Medical and R&D Organizations including the Finance and Business Support Team, and perform other duties as assigned JOB REQUIREMENTS: Organizations including the Finance and Business Support Team, and perform other duties as assigned. QUALIFICATIONS: BA/BS Degree in Business Administration, Economics, Finance or related field. Minimum 1-2 years of biotechnology or pharmaceutical experience is required, finance experience preferred. Experience in developing business models for decision support and business planning is highly desirable. Excellent PC skills, good interpersonal communication, excellent organization skills and has the drive for results. If you are interested in this position please click the Apply Now button below and search for Req #. 02043. MedImmune is an Equal Opportunity Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, veteran status, or any other characteristic protected by federal, state or local law. http://www.newscientistjobs.com/jobs/job/operations-analyst-i-md-maryland-200619538.htmFri, 23 Oct 2009 14:11:37 +0000149648My company shares my passion for helping to improve human health around the world.” “This is My MedImmune.” Those who join MedImmune feel a sense of ownership about their future. They thrive with a recognized leader in the biotechnology industry and the wholly-owned subsidiary of AstraZeneca plc. Here, you will join passionate professionals who advance science, technology and medicine to develop products designed to help people live better lives. You will excel in an environment characterized by respect, integrity and growth opportunities…that encourages both individual contribution and collaborative entrepreneurial thinking. Our products and/or product candidates are designed to address areas of need in infection, oncology, respiratory disease and inflammation, cardiovascular/gastrointestinal disease and neuroscience. Explore a MedImmune career as we strive to better more lives, more often, around the world. Title: Operations Analyst I Location: MD, Gaithersburg - Corporate Headquarters Req: 02043 Primary responsibilities will include participating in special projects to effectively assist the Medical Organization with key decision support in managing the business operations, oversight of the Medical Organization invoice process, tracking, reporting and training of other Medical Organization personnel on invoice processing, and coordinating as necessary, in the business plan and evaluation of risks and opportunities with upper management, resourcing analysis, InSight reporting and resource planning maintenance and updates. Duties include coordination and management of the Medical Organization invoice review and approval process. Develop and provide department heads and clinical operations team with detailed reporting to assist in the management of outstanding invoices and disputes. Involve in all aspects of the invoice process for the Medical Organization, including the review and update of the work process documents, process improvement initiatives and maintenance of the central MedOrg Invoices helpdesk email box. Perform ad hoc analyses, as required with general supervision from Manager, Medical Operations. Participate in the development of business models and metrics for the Medical Organization and will eventually assist in the consolidation of the Performance Metrics Summary for upper management. This position will work on simple to complex problems where the ability to assess and analyze situations, to adapt to the changing environment of the business, and to create efficiencies in managing the process are fundamental. With general supervision from the Manager, Medical Operations, this position will lend support to the overall business operations activities managed and directed within the Resource Performance Management group, in addition to the various cross-functional teams within the Medical and R&D Organizations including the Finance and Business Support Team, and perform other duties as assigned JOB REQUIREMENTS: Organizations including the Finance and Business Support Team, and perform other duties as assigned. QUALIFICATIONS: BA/BS Degree in Business Administration, Economics, Finance or related field. Minimum 1-2 years of biotechnology or pharmaceutical experience is required, finance experience preferred. Experience in developing business models for decision support and business planning is highly desirable. Excellent PC skills, good interpersonal communication, excellent organization skills and has the drive for results. If you are interested in this position please click the Apply Now button below and search for Req #. 02043. MedImmune is an Equal Opportunity Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, veteran status, or any other characteristic protected by federal, state or local law. http://www.newscientistjobs.com/jobs/job/rd-associate-iii-md-maryland-200619499.htmFri, 23 Oct 2009 13:59:58 +0000149646My company shares my passion for helping to improve human health around the world.” “This is My MedImmune.” Those who join MedImmune feel a sense of ownership about their future. They thrive with a recognized leader in the biotechnology industry and the wholly-owned subsidiary of AstraZeneca plc. Here, you will join passionate professionals who advance science, technology and medicine to develop products designed to help people live better lives. You will excel in an environment characterized by respect, integrity and growth opportunities…that encourages both individual contribution and collaborative entrepreneurial thinking. Our products and/or product candidates are designed to address areas of need in infection, oncology, respiratory disease and inflammation, cardiovascular/gastrointestinal disease and neuroscience. Explore a MedImmune career as we strive to better more lives, more often, around the world. Title: R&D Associate I/II Location: MD, Gaithersburg - Corporate Headquarters Req: 01973 Position Summary: Major Duties and Responsibilities (including supervising others): As a member of a cell culture process development team, candidate will participate in designing and conducting various experiments in shake flasks and bench-scale bioreactors to develop and improve processes for production of recombinant antibodies and other protein therapeutics. In addition to process development, this role will require the candidate not only to participate in various research projects for technology development in cell culture process but also to conduct his/her own projects to improve the current media formulation or cell culture procedures, such as wave bioreactor process and cell banking. Candidate will also be expected to design and run experiments for troubleshooting general issues related to cell culture processes as needed. Other duties and responsibilities include data analysis, presentation of analyzed data in internal meetings and collaborating with other members of the group for Operational Excellence projects Special Skills/Abilities: Candidates with following skills are preferred: Aseptic techniques, Mammalian cell culture, Operation and maintenance of bench scale bioreactors, media preparation. Candidates are also expected to have solid data analysis and communication skills Job Complexity: Occasional weekend work is required. Must be able to perform multiple experiments simultaneously and analyze data with some supervision. Supervision: No supervisory role (Supervision required, level of independence) JOB REQUIREMENTS: Education: B.S. or M.S in Chemical Engineering, Life Science or other related fields Experience: Research Associate I position requires 0–2 years with a B.S. degree and Research Associate II position requires 2–5 years with a B.S, or 0–2 years with an M.S.degree. If you are interested in this position please click the Apply Now button below and search for Req #. 01973. MedImmune is an Equal Opportunity Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, veteran status, or any other characteristic protected by federal, state or local law. http://www.newscientistjobs.com/jobs/job/sirna-formulations-scientist-ma-massachusetts-200613729.htmFri, 16 Oct 2009 15:42:24 +0000142851Chemical and Pharmaceutical Profiling is seeking a scientist to integrate into the existing formulation/delivery group conducting research into the Novartis therapeutic siRNA initiative. Primary research goals will be drug delivery technology evaluation and application to the delivery challenge posed by therapeutic siRNA. Both systemic and local delivery methods will be explored for a diverse array of disease indications. Hands-on responsibilities will include the development of new formulation reagents, new oligonucleotide conjugation reagents, support the exploration of polymer-based delivery systems, and the development of predictive analytical and in vitro assays. Skills in tangential flow filtration, analytical/semi-preparative HPLC, and mass spectroscopy are desirable. Ability to provide technical consultation for complex projects and/or complex technical issues and will provide coaching and mentoring for associates. Can work independently and interact with a team of multidisciplinary backgrounds including medicinal chemistry, biologists, pharmacologists, and external collaborators. Excellent oral and written communication and presentation skills. Specific experience with development of polymer-based/lipid gene delivery systems and/or oligonucleotide analytical development is desirable. http://www.newscientistjobs.com/jobs/job/postdoctoral-associate-microfluidics-specialist-va-virginia-200611265.htmFri, 16 Oct 2009 13:40:19 +0000142720The 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/directorsenior-director-rd-of-viology-md-maryland-200608832.htmMon, 12 Oct 2009 14:46:41 +0000138709My company shares my passion for helping to improve human health around the world.” “This is My MedImmune.” Those who join MedImmune feel a sense of ownership about their future. They thrive with a recognized leader in the biotechnology industry and the wholly-owned subsidiary of AstraZeneca plc. Here, you will join passionate professionals who advance science, technology and medicine to develop products designed to help people live better lives. You will excel in an environment characterized by respect, integrity and growth opportunities…that encourages both individual contribution and collaborative entrepreneurial thinking. Our products and/or product candidates are designed to address areas of need in infection, oncology, respiratory disease and inflammation, cardiovascular/gastrointestinal disease and neuroscience. Explore a MedImmune career as we strive to better more lives, more often, around the world. Director/Senior Director, R&D of Viology Location: Gaithersburg, MD Req #: 1876 Director of Infectious Disease We are seeking a senior virologist who will be responsible for leading and managing a team of 10+ researchers in the development of large molecule drugs against viral pathogens. This individual will be responsible for supporting and enhancing the portfolio of antiviral biologics by effectively directing their scientific staff in the progression of projects through various preclinical stages of drug development. This individual will also act as project leader of some cross-functional teams. In addition, he/she will be responsible for identifying and assessing new targets for large molecule drugs against viruses, and will participate in the development of department strategy. This individual will be expected to provide scientific insight, and to effectively represent his/her team both inside and outside MedImmune. He/she will be expected to initiate and maintain collaborations with research scientists in other therapeutic areas at MedImmune, and with scientists in the larger Astra Zeneca organization. JOB REQUIREMENTS: Job requirements: • Ph.D. in virology, biology, immunology, biochemistry or related discipline • 7 – 10 years relevant industrial experience developing large or small molecule drugs or vaccines against viral pathogens • In depth knowledge of virology, especially respiratory pathogens • Extensive experience leading and directing scientists in the design and execution of experiments to assess the in vitro and in vivo efficacy of antiviral therapeutics and/or vaccines • Experience with all stages of the drug development process: target identification and validation, lead isolation and optimization, pre-clinical development • The ability to prioritize, and to develop and implement research plans that are aligned with department priorities • Proven ability to balance multiple, and often competing, priorities and timelines • The ability to initiate and maintain scientific collaborations, and interact effectively with personnel outside research (e.g., Clinical, Regulatory Affairs, Business Development). • Significant experience managing scientists at different levels (i.e., junior and senior staff) • Strong personnel management skills • Excellent written, verbal and presentations skills • Ph.D. in virology, biology, immunology, biochemistry or related discipline If you are interested in this position please click the Apply Now button below and search for Req #. 01876. MedImmune is an Equal Opportunity Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, veteran status, or any other characteristic protected by federal, state or local law. http://www.newscientistjobs.com/jobs/job/manager-rd-strategic-sourcing-md-maryland-200607570.htmFri, 09 Oct 2009 20:47:56 +0000136597My company shares my passion for helping to improve human health around the world.” “This is My MedImmune.” Those who join MedImmune feel a sense of ownership about their future. They thrive with a recognized leader in the biotechnology industry and the wholly-owned subsidiary of AstraZeneca plc. Here, you will join passionate professionals who advance science, technology and medicine to develop products designed to help people live better lives. You will excel in an environment characterized by respect, integrity and growth opportunities…that encourages both individual contribution and collaborative entrepreneurial thinking. Our products and/or product candidates are designed to address areas of need in infection, oncology, respiratory disease and inflammation, cardiovascular/gastrointestinal disease and neuroscience. Explore a MedImmune career as we strive to better more lives, more often, around the world. Title: Manager, R&D Strategic Sourcing Location: MD, Gaithersburg - Corporate Headquarters Req: 01993 Major Duties and Responsibilities (including supervising others): • Collaborate with business partners to create and execute category plans utilizing “best in class” strategic sourcing strategies and methodologies • Lead cross functional teams sourcing projects through all key phases such as data collection & analysis, strategy development, RFx, award recommendation, contract negotiation & execution and implementation • Drive continuous improvement in process, price, service, etc. through effective category management • Develop category specific goals and objectives • Study and track market dynamics to determine impact on cost, quality and risk • Manage “key” supplier relationships and optimize supply base • Negotiate contracts and collaborate with legal to establish optimal terms and conditions, pricing and key performance indicators • Monitor and report category-specific savings and performance metrics • Facilitate annual supplier reviews Special Skills/Abilities: • Exceptional track record of building relationships with stakeholders • Demonstrated proficiency influencing people, problem solving and decision making • Excellent communication and project management skills • Superior project management skills • Advanced Excel and PowerPoint skills • SAP a plus JOB REQUIREMENTS: Job Complexity: This is a highly complex position. The candidate will be required to “win” the trust of stakeholders, establish strong relationships and drive stakeholder value all while impacting the “bottom line”. Supervision: The candidate will be a highly experienced individual contributor. He/she will be empowered to independently drive results. Strategy will be determined through collaboration of Sourcing management and stakeholder input. Requirements/Qualifications: Education: Bachelor’s degree in business or a related field such as Supply Chain, Business, Economics, Finance, or other. MBA or JD a plus. Experience: • Minimum of 5 – 7 years strategic sourcing for Pharmaceutical, Consumer Package Goods, Heath and Beauty Aides or other like industries • Demonstrated success sourcing a broad range of goods and services such as but not limited to the following: o MRO / Industrial & Safety Supplies o Professional Services IT and/or♣ Business Consulting Financial Consulting / Audit♣ o Clinical Research o Direct Materials o Advertising & Promotion o Small and/or Large Capital Expenditures If you are interested in this position please click the Apply Now button below and search for Req #. 01603. MedImmune is an Equal Opportunity Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, veteran status, or any other characteristic protected by federal, state or local law. http://www.newscientistjobs.com/jobs/job/rd-associate-iii-md-maryland-200599542.htmWed, 07 Oct 2009 16:41:22 +0000133361My company shares my passion for helping to improve human health around the world.” “This is My MedImmune.” Those who join MedImmune feel a sense of ownership about their future. They thrive with a recognized leader in the biotechnology industry and the wholly-owned subsidiary of AstraZeneca plc. Here, you will join passionate professionals who advance science, technology and medicine to develop products designed to help people live better lives. You will excel in an environment characterized by respect, integrity and growth opportunities…that encourages both individual contribution and collaborative entrepreneurial thinking. Our products and/or product candidates are designed to address areas of need in infection, oncology, respiratory disease and inflammation, cardiovascular/gastrointestinal disease and neuroscience. Explore a MedImmune career as we strive to better more lives, more often, around the world. Title: R&D Associate I/II Location - Gaithersburg, MD Req #: 1603 Perform formulation development, optimization, product characterization and stability studies of protein therapeutics. Design and execute experiments to support preformulation, formulation screening, biophysical characterization studies, container closure compatibility studies and lyophilization development studies. Write protocols, analyze data, interpret results, prepare technical reports and present findings in department and inter-department meetings. Support fill/finish operations and technology transfer to manufacturing for clinical and commercial products. Special Skills/Abilities: Experience with protein formulation development, biophysical characterization techniques such as calorimetry, fluorescence spectroscopy and HPLC is preferred. Experience in lyophilization development and GMP fill/finish operations would be advantageous. Good communication skills, strong interpersonal skills, demonstrated leadership qualities, and the ability to thrive in an interdisciplinary fast-paced environment are also an integral part of this position. JOB REQUIREMENTS: Education: M.S. or B.S. in Chemistry, Biochemistry, Pharmaceutics, Chemical Engineering or related field. Experience: 0-3 years experience in the biopharmaceutical industry desired If you are interested in this position please click the Apply Now button below and search for Req #. 01603. MedImmune is an Equal Opportunity Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, veteran status, or any other characteristic protected by federal, state or local law. http://www.newscientistjobs.com/jobs/job/manager-clinical-maintenance-md-maryland-200580551.htmMon, 28 Sep 2009 20:51:10 +0000125379My company shares my passion for helping to improve human health around the world.” “This is My MedImmune.” Those who join MedImmune feel a sense of ownership about their future. They thrive with a recognized leader in the biotechnology industry and the wholly-owned subsidiary of AstraZeneca plc. Here, you will join passionate professionals who advance science, technology and medicine to develop products designed to help people live better lives. You will excel in an environment characterized by respect, integrity and growth opportunities…that encourages both individual contribution and collaborative entrepreneurial thinking. Our products and/or product candidates are designed to address areas of need in infection, oncology, respiratory disease and inflammation, cardiovascular/gastrointestinal disease and neuroscience. Explore a MedImmune career as we strive to better more lives, more often, around the world. Title: Manager, Clinical Maintenance Location: MD, Gaithersburg - Corporate Headquarters Req: 01947 Position Summary: Responsible for managing the design and implementation of office, manufacturing, research processes, instrumentation and equipment from the laboratory through pilot plant and manufacturing scale. Plans, budgets and schedules facility modifications including estimates on equipment, labor, materials, utilities and other related costs. Develops and implements annual departmental expense/capital plans. Provides expertise in office, research, manufacturing, engineering, design and process design/scale-up. Assists the manufacturing/research operations in problem solving with regards to equipment and systems. Develops capital expenditure requirements and documentation to purchase/install new systems/equipment/processes. Develops and recommends new processes and technologies to achieve cost effectiveness and improved product quality. Recommends processes for the production of therapeutic products. Establishes operating equipment specifications and improves manufacturing techniques. Involved in new product scale-up, process optimization, technology transfer, and process validation activities. Interfaces with various departments to ensure processes and designs are compatible for new product technology transfer and to establish future process and equipment automation technology. Supports company growth with space optimization and construction management for new/renovated manufacturing, research and administrative areas. Oversees the coordination of building space allocation and layout, communication services and facilities expansion. Essential Job Functions: Carries out managerial responsibilities in accordance with organizational policies, procedures, and state, federal and local laws. Oversees and manages departmental activities in regards to both planned and unplanned maintenance utilizing a Computerized Maintenance Management System such as Maximo. Ensures that all department activities are performed and documented accurately and are in compliance with SOP’s, cGXP, and FDA requirements (cGMP). Assures the appropriate level of cGMP/cGXP training for all maintenance staff, following corporate guidelines and policies. Develops metrics to measure department performance. Supports and promotes corporate, site vision and mission statements, and goals. Additional Job Functions: • Develop and implement goals, objectives and best practices • Ability to change the thinking of or gain acceptance of others in sensitive situations. • Ability to develop, utilize and execute project management • Ability to multitask and manage multiple projects. • Establish and maintain a cooperative and positive relationship with other departments • A thorough understanding of all utility and manufacturing equipment • Good management and practices principals • Solid team building practices • Develop departmental spending budgets following corporate guidelines • Excellent written and verbal communication skills • Proficient in computer skills and MS Office application • Experience in maintenance trades and knowledge of building codes. • Coordination of reports to monitor Building Management System for facility critical alarms/equipment to ensure that adequate and timely response is maintained 24/7. • Available 24/7 to direct and coordinate emergency issues that may arise. • Responsible for VSCRs, Deviations, SOPs in responsible area of control. • Development of routine reports. • Review and response to building system reports. • Reviews design and construction documents for new site projects. Freedom to Act Assignments are received in task-and objective-orientated terms. Provides direction to subordinates based on general policies and management guidelines. Work is reviewed upon completion for adequacy in meeting objectives. Interprets and executes policies and procedures that typically affect subordinate organizational units. Recommends modifications to operating policies. Supervisor Relationships Accomplishes results through lower-level subordinate supervisors, leads or through experienced exempt/non-exempt employees who exercise significant latitude and independence in their assignments in terms of costs, methods and employees. Often heads a centralized functional activity. Operations Involvement / Direct Work Involvement Responsible for all projects assigned to the organizational unit. Acts as an advisor to subordinate supervisors, leads or staff members to meet schedules or resolve technical or operational problems. Directly participates in establishing and administering many centralized functional projects. Develops and administers budgets, schedules, and performance standards. Impact Ensures that projects/work plans are completed on schedule and within budget. Erroneous decisions or recommendations or failure to complete assignments would normally result in serious delays to assigned projects resulting in considerable expenditure of additional time, human resources, and funds. . Erroneous decisions will result in critical delay(s) in schedules and/or unit operations and may jeopardize overall business activities. Liaison Frequent contacts with internal personnel and outside customer representatives at various management levels concerning operations or scheduling. JOB REQUIREMENTS: Typical Education: Bachelors degree in Engineering (5 – 10 years) or Masters Degree in Engineering (2 –5 years) desired. Work history (ie Department supervisor), may be substituted for technical degree (10+yrs experience in a cGXP environment, in a supervisory role) Typical Experience: 5 – 10 years Certificates, Licenses, Registrations: N/A Technical Knowledge: Pharmaceutical systems, industrial utilities, process equipment, GMP, GXP, HVAC, General Construction Practices, Maintenance Software, Building Management Systems Computer Skills: Outook, Internet Explorer, Capability to Utilize Various Programs Developed for Day to Day Maintenance Operations, Specialty Maintenance PM Software, MS Office Programs (Excel, Word, Projects, etc.) Job Complexity: Job has a high degree of technical complexity and requires in-depth understanding of systems, programming languages and interface capabilities. This position requires a meticulous attention to detail. Supervision: This individual will report directly to Senior Manager on the Business Analytics team, but requires a high degree of independence and initiative and ability to self-start with little direction If you are interested in this position please click the Apply Now button below and search for Req #. 01947. MedImmune is an Equal Opportunity Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, veteran status, or any other characteristic protected by federal, state or local law. http://www.newscientistjobs.com/jobs/job/nasa-postdoctoral-fellowships-al-alabama-200402589.htmTue, 07 Apr 2009 14:43:10 +00009858NASA Postdoctoral Fellowships The NASA Postdoctoral Program (NPP) offers unique research opportunities to highly talented national and international scientists to engage in ongoing NASA research in space science, earth science, aeronautics, space operations, exploration systems, and astrobiology. Awards: • Approximately 50 Fellowships awarded annually • One-year appointments, renewable up to three years • Annual stipends start at $50,000, with supplements for specific degree fields and high cost-of-living areas • Annual travel budget of $8,000 • Financial assistance for relocation • Financial supplement for health insurance purchased through the program • Apply at http://nasa.orau.org/postdoc Application Deadlines: Three each year - March 1, July 1, and November 1 Eligibility: • U.S. Citizen • Foreign Nationals with a J-1 visa status as a research scholar, Lawful Permanent Resident (LPR) status, or Employment Authorization Document (EAD with pending LPR status • Recent and senior-level Ph.D. recipients Locations of Fellowship Positions: • Ames Research Center, Moffett Field, CA • Dryden Flight research Center, Edwards, CA • Glenn Research Center, Cleveland, OH • Goddard Space Flight Center, Greenbelt, MD • Jet Propulsion Laboratory, Pasadena, CA • Johnson Space Center, Houston, TX • Kennedy Space Center, Kennedy Space Center, FL • Langley Research Center, Hampton, VA • Marshall Space Flight Center, Huntsville, AL • Stennis Space Center, Stennis Space Center, MS • NASA Headquarters, Washington, DC • Various locations associated with the NASA Astrobiology Institute To obtain more information and to apply for this exciting opportunity, please visit the NPP Web site at http://nasa.orau.org/postdoc