http://www.newscientistjobs.com/jobsNew Scientist Jobshttp://www.newscientistjobs.com/jobs/job/research-associate-iii-ca-california-200645870.htmFri, 20 Nov 2009 19:22:09 +0000196352My 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: Research Associate I/II Location: CA, Santa Clara - NON SALES Req: 02076 Major Duties and Responsibilities (including supervising others): Development and/or optimization of virus upstream processes (from cell thaw through viral harvest). This includes designing experiments, analyzing data, developing batch records, SOPs and protocols, and writing and/or reviewing technical reports. This may also include the evaluation of alternative methodologies and/or materials for various process operations and steps. Serve as a member of the team responsible for the technology transfer of processes to large scale manufacturing sites. This includes writing and/or review of batch records and contract manufacturing staff, and providing the necessary technical support to the contract manufacturer once the process has been transferred and cGMP manufacturing has begun. Maintenance of upstream process development equipment including bioreactors, cell counters, metabolite analyzers, pumps and gauges. Maintenance of inventory for commonly used lab supplies. Other responsibilities as required by the department or team. JOB REQUIREMENTS: Requirements/Qualifications: Education: B.S. in Engineering Experience: 2-5 years Special Skills/Abilities: Bioreactor operation Job Complexity: Cell culture in Biolevel 2 labs Supervision: Supervision required If you are interested in this position please click the Apply Now button below. Req #. 01889 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/associate-scientist-iiscientist-i-md-maryland-200645868.htmFri, 20 Nov 2009 19:16:57 +0000196350My 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: Associate Scientist II/Scientist I Location: CA, Mountain View - NON SALES Req: 02056 Position Summary: Major Duties and Responsibilities (including supervising others): We are seeking a highly motivated independent individual to join our formulation team aimed at formulation development for biologics including protein and live viruses. The individual will be working with the team focusing on formulation studies and characterizations for liquid or solid dosage formulations. The essential responsibilities will include planning and executing pre-formulation and formulation studies, developing and performing biophysical, biochemical and biological analyses. An ability to work independently and have effective organization and communication skills is essential. Special Skills/Abilities: Expertise in pre-formulation and formulation of proteins and antibodies required. Hands on expertise in analytical techniques including HPLC-SEC, RP-HPLC, FTIR, fluorescence assays, DSC/mDSC are required. A prior experience in ajuvant formulation development is a plus. Experiences with solid state analyses such as Karl-Fischer, TGA, DVS, particle sizing desired. Excellent oral and written skills required. Job Complexity: Medium-High. JOB REQUIREMENTS: Supervision: Work is performed with minimal supervision. (supervision required, level of independence) Requirements/Qualifications: Education: Degree in Chemistry, Chemical Engineering, Pharmaceutical Sciences, Biochemistry, Biophysics. Experience: Ph.D. + 0-3 yrs, M.S. + 8-10 yrs, B.S. + 10-13 yrs. If you are interested in this position please click the Apply Now button below. Req #. 02005 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/validation-officer-kent-200645727.htmFri, 20 Nov 2009 16:54:15 +0000196080We are currently looking for a Validation Officer to join a leading Biotechnology company based in the Kent region. Purpose of the role To undertake various validation activities assigned by Validation Manager. Key Responsibilities To prepare, execute and report validation protocols Responsibilities include the validation of: * Equipment (Protocol Writing, Execution, Report Writing / Approval) * Production Processes (Protocol & Report Writing / Approval) * Analytical Methods (Protocol & Report Writing / Approval) * Facilities and Utilities (Protocol & Report Writing / Approval) * Computer Systems (Protocol & Report Writing / Approval) * Cleaning Studies (Protocol & Report Writing / Approval) * Shipping Studies (Protocol & Report Review/ Approval) Establish and maintain the re-qualification schedule for validated equipment. To perform temperature mapping of refrigerators, freezers and incubators. Liaise with Engineering, Quality Assurance and User Departments to ensure that validation is conducted in a timely manner with minimal disruption to production. Ensure that the necessary documentation in place and current to control all aspects of validation. Review of Manufacturing Procedures to ensure that appropriate validation work has been completed prior to approval of the procedure. Co-ordinate validation documentation systems in conjunction with QA. Attend meetings, both internal and external, representing the department in a professional manner. Participate in audits by customers and regulatory authorities. To ensure that safe working methods and practices are adopted at all times and in accordance with Company policy for the safety of the postholder and others within the working environment. To be responsible for housekeeping, tidiness and general cleanliness of all areas in which the post holder is working. To assist in training of other staff as required. Scope/Impact Works independently under general supervision and direction. Work is reviewed for soundness of judgment and overall adequacy and accuracy. Performs work that consistently requires independent decision making and the exercise of independent judgment and discretion. It is important that the post holder is self motivated and can manage multiple tasks. Knowledge, skills and experience required Degree level, preferably in Chemistry, Biology, Engineering or a Related Subject Understanding of ISO 9000 Quality System Knowledge of cGMP General understanding of IQ, OQ, PQ, PV. Temperature mapping. Understanding of Cleaning validation. Ability to author and execute validation reports. Ability to write validation related procedures. Understanding of calibration principles. Use of Microsoft Word, PowerPoint and Excel. To apply for this position, candidates must be eligible to live and work in the UK Matchtech Group Plc is acting as an Employment Agency in relation to this vacancy. http://www.newscientistjobs.com/jobs/job/postdoctoral-research-fellowship-cryogen-based-energy-storage-leeds-200645671.htmFri, 20 Nov 2009 16:29:48 +0000195951Faculty of Engineering School of Process, Environmental and Material Engineering Institute of Particle Science and Engineering Full-time, fixed term for twenty four months The focus of the post is to develop an energy storage system based on the use of cryogen as an energy carrier. The work will involve construction and testing of a lab-scale energy storage system, and theoretical analyses and modeling of the system. With at least a 2:1 degree (or equivalent) in Cryogenic Engineering, Mechanical Engineering, Chemical Engineering, Thermophyics or other related science and engineering disciplines you will also have a PhD (or be close to completing) in one of the above disciplines. Preference will be given to those with a solid background, strong experimental skills and demonstrable track record in at least three of the following: Engineering thermodynamics Heat transfer Fluid mechanics Cryogenic engineering Refrigeration University Grade 7 (£29,704 - £35,469 p.a.) Informal enquires to Professor Yulong Ding tel +44 (0)113 343 2747 email y.ding@leeds.ac.uk To download an application form and job details please click the Apply Now button below. Alternatively these may be obtained from Carly Hancock on the number listed within the 'View Contact Details' section below. Job ref 312405 Closing date 4 January 2009 It is anticipated that interviews will be held mid January 2010 http://www.newscientistjobs.com/jobs/job/qualification-technologist-materials-cambridgeshire-20k-cambridgeshire-200645456.htmFri, 20 Nov 2009 15:30:37 +0000195550Qualification Technologist - Composite Materials - Cambridgeshire - circa £20k This is a great opportunity for an engineering graduate with knowledge of material science to join the world's leading producer of composite materials. Our client is a multi-national company with headquarters in the US and facilities around the world. As Qualifications Technologist you will be based at their site in Cambridgeshire and will join a team involved in the qualification of company products and materials from across their European and Pacific Rim sites. If you have an enthusiasm to lean and continue with your development, this opportunity represents the chance to gain superb experience within a fast growing manufacturing business. The key activities for this role will involve: - Project preparation and planning - Writing full technical reports - Reading and vetting external specifications - Preparation of specimens - Testing the physical and mechanical properties of the materials using a variety of techniques - Analysis and reporting of results - Further understanding and exploration of composite materials and their structures To be considered for this excellent opportunity you will require the following Qualification, Skills and Experience: - Minimum qualification Degree level (or equivalent) in Engineering, preferably with knowledge of materials science - Ability to probe and analyse data with good problem solving and reasoning skills - Confident communicator, articulate with good report writing abilities - Sound and proven ability to manage multiple projects - Practical material / mechanical testing experience - Background in composite materials or polymers would be ideal Salary circa £20k + excellent benefits package that includes bonus scheme, share options and contributory pension. http://www.newscientistjobs.com/jobs/job/clinical-research-project-manager-medical-devices-iso-14155-north-west-200645424.htmFri, 20 Nov 2009 15:13:20 +0000195490Clinical Research Project Manager - Medical Devices - ISO 14155 - North West A growing Medical Devices company in the North West are currently looking to recruit a Clinical Research Project Manager due to the success of the company's products and the growth of the organisation. As you will be leading the Clinical Trials of the Medical Trials you will be working to ISO 14155 standards and running projects in to the same procedures. You will be leading the Clinical Trials and be in charge of a number of members of staff while running the trials, due to this, communication skills to all levels of staff is important and experience working as a Project Manager will be advantageous. You must have experience of working on Medical Device Clinical Trials to ISO 14155 standards and to Medical Device Directive (93/42/EEC). As you will be meeting with people from all different countries you will need to have very strong spoken and written communication skills as well as a history of presenting your teams results. It is required for you to have a 2:1 or 1st degree in Life Sciences or a similar discipline to keep in line with the rest of the organisation. As this is a senior position in the company you will need a few years experience working on Medical Devices in the Clinical Research field and working in ISO 14155 guidelines. This is an expanding organisation offering the right person unlimited opportunity to develop their career. You will also be rewarded with very generous salary and excellent benefits. Interviews are already underway so to register your interest in this role please submit an application now. If you would like some more information about the position please call myself, Andrew Welsh of Paramount Recruitment, on 0121 616 3463. Paramount Recruitment Limited provides services as an agency and an employment business. We regularly have similar roles in this area. Please see our website for details or send your CV in to us to find out the latest opportunities. http://www.newscientistjobs.com/jobs/job/assay-development-quality-engineer-lateral-flow-midlands-200645421.htmFri, 20 Nov 2009 15:09:46 +0000195479Assay Development Quality Engineer - Lateral Flow - Medical Devices - ISO 13485 - East Midlands A very exciting opportunity has become available for a Assay Development Quality Engineer who can their experience with lateral flow. You will be based in the East Midlands. This is the perfect opportunity for someone with strong lateral flow, Raw Materials and Assay Development experience in the Medical Devices sector. You will be joining an expanding company with a really ideal to recruit the best and supply the best working environment. This company is a spin off organisation of one of the largest Medical Devices in the UK and has major financial and industry backing. The site is a very modern facility with top of the range equipment allowing you to succeed in your job at the minimum of ease. There is an excellent training system in place allowing people to improve their skills and ultimately be a part of the organic growth the company is producing. You must have experience with lateral flow within the Medical Devices sector. You will be provided with all the support required and this is a great company to have on your CV that will open other opportunities in the future. It will be ideal if you have experience working within Vitro Diagnostics and have been Process Monitoring or Validation Requirements. Apply now to arrange your interview. For more information please call myself, Andrew Welsh of Paramount Recruitment, on 0121 616 3463. Assay Development, Raw Material, Quality Engineer, ISO 13485, In Vitro Diagnostic, Validation Requirement, Process Monitoring Paramount Recruitment Limited provides services as an agency and an employment business. We regularly have similar roles in this area. Please see our website for details or send your CV in to us to find out the latest opportunities. http://www.newscientistjobs.com/jobs/job/electromagnetic-engineer-scientific-research-facility-leicestershire-200645419.htmFri, 20 Nov 2009 15:08:38 +0000195478Electromagnetic Engineer - Scientific Research Facility - Leicestershire A cutting edge Scientific Research Facility in Leicestershire is keen to bring on in an experienced Electromagnetic Engineer. You will be working on a number of electromechanical projects and Magnetic Fields. The company are currently working on a number of critical projects and require someone to be a key part of the process and business. Due to the success of this company there is guaranteed work for years to come and high job security. You will be in a department that works with a lot of Electromechanical, Electromagnetic, Magnetic and Mechatronic projects. It will be ideal to have as much knowledge in these areas as possible. You will be doing a lot of Mathematical Modelling and Prototype building of systems, due to this it will be ideal for you to have experience modelling with Opera or CPS systems. This is the opportunity to join a company who are involved with ground breaking research projects that will aid you career in years to come. They are offering very strong job security, a very strong salary and benefits. As the company is growing this is an exciting time to join and really start a productive career. Interviews are already being arranged, so apply now to enter the process. For more information on the position please call myself, Andrew Welsh of Paramount Recruitment, on 0121 616 3463. Paramount Recruitment Limited provides services as an agency and an employment business. We regularly have similar roles in this area. Please see our website for details or send your CV in to us to find out the latest opportunities. http://www.newscientistjobs.com/jobs/job/electronics-engineer-scientific-research-and-development-cambridgeshire-200645417.htmFri, 20 Nov 2009 15:06:09 +0000195476Electronics Engineer - Scientific Research and Development - Cambridgeshire Leading Research and Development Consultancy Firm in the Cambridgeshire area are currently looking for an experienced Electronics Engineer to start ASAP to work on a multitude of projects. You will be working for one of the largest Consultancy firms with a major presence in the global marketplace. You will be working close with Mechanical Engineers, Design Developers and Project Managers to assist in the development of key projects. This company is very active in creating new business and already has a very strong client base for years to come. You will be working as a part of a unit so it will be important to have worked under the directorship of Project Managers before. As this company works on cutting edge Scientific Projects it will be advantageous if you have worked on Scientific Devices in the past. You will need to have been developing electronic systems for a while and have a 1st or 2:1 degree in electronics, computer sciences or a similar subject. This role will reward you with the opportunity to develop your career to new heights, an excellent starting salary and benefits. Interviews are already in process so apply now to register your interest. For more information please call myself, Andrew Welsh of Paramount Recruitment on 0121 616 3463. Paramount Recruitment Limited provides services as an agency and an employment business. We regularly have similar roles in this area. Please see our website for details or send your CV in to us to find out the latest opportunities. http://www.newscientistjobs.com/jobs/job/production-manager-lean-internal-client-facing-cambridge-cambridgeshire-200645416.htmFri, 20 Nov 2009 15:04:15 +0000195471Production Manager - LEAN - Internal Client Facing - Cambridge There is an exciting opportunity for an expert in LEAN manufacturing principles to join a scientific organisation that are looking to progress there working practices into the modern era. You will be working as a Production Manager and will be working with the shop floor and the senior management. As you will be working with internal clients implementing massive organisational changes it will be advantageous if you have experience as a LEAN Consultant, it will also be ideal if you have working knowledge as a LEAN Manufacturing Engineer. This company has been running for over thirty years and is looking to expand and grow as an organisation. It is an exciting time to join as you will get the opportunity to be a driving force of the change and also be a senior member of staff in the future. Apply now as interviews are already in process. For more information please call myself, Andrew Welsh of Paramount Recruitment, on 0121 616 3463. Paramount Recruitment Limited provides services as an agency and an employment business. We regularly have similar roles in this area. Please see our website for details or send your CV in to us to find out the latest opportunities. http://www.newscientistjobs.com/jobs/job/head-of-regulatory-affairs-republic-of-ireland-200642724.htmFri, 20 Nov 2009 13:13:02 +0000194667An exciting opportunity has arisen in a Global Multinational Medical Device Company based in Dublin. This position will be responsible for ensuring that regulatory compliance of all medical device products placed on the market under the Irish transposition of the Medical Device Directive 93/42/EEC is achieved and maintained. Role: Leading the Regulatory Affairs Department to ensure the Company's continuous compliance with the following regulatory standards: o The FDA Quality System Regulation 21 CFR 820 (QSR). o The Medical Devices Directive 93/42/EEC. o Health Canada Medical Devices Regulations. o ISO 13485 Quality Management Systems Requirements for Medical Devices. o ISO 9001 Quality Management Systems Requirements. o Various World Wide Regulations. Essential responsibilities: o Recall / Vigilance-including customer communications, root cause investigations, regulatory agency communication, corrective action implementation and effectiveness checks. o Sit as a member of the Complaint Review Team (CRT). o Represent Regulatory Affairs as part of a Design Control Project. o New product submissions. o Represent Regulatory Affairs as part of a Design Change Control, including validation of new processes, raw materials, overseeing Cross Functional Teams. o World Wide Product Registration. o Providing strategy and guidance on Product Labelling and Packaging. o Ensure compliance of CE-marking Files, Design History Files, CE-marking Activities. o Material Safety Data Sheets (MSDS). o Responsible for ensuring quarantine of product (post market). o Review of Customer Literature. o Customer Post Market Surveillance. o Review and Approval of Instrument Application Validation in accordance with applicable regulations. o Site Wide Training on Regulations. o Research and Assess the impact to the Company of new regulations. o Original Equipment Manufacturer (OEM) Process. o Documenting Health Hazard Assessment & Clinical Risk Assessment. Qualifications: o Preferably 5 years industrial experience. o Preferably 5 years management experience. o Primary degree qualification in a science related discipline or equivalent in terms of relevant operational experience. ************************************************************** For Immediate Consideration Please Apply Online Now If you would like further information before applying please contact: Brian Christensen BA(Mod.)MedChem on +353 1 685 4747 Your details will not be passed to a Third Party without your express Prior Consent. View our Privacy Policy http://www.newscientistjobs.com/jobs/job/head-of-research-and-development-republic-of-ireland-200642732.htmFri, 20 Nov 2009 13:13:00 +0000194670Rer no: 0910-13 POSITION RESPONSIBILITIES: o Lead a group of technical staff (approximately 10 personnel) in the definition, development and commercialization of catheter based technologies/devices in line with the company strategy. o Coordinate the activities of engineers in the solution of complex product and process development problems using engineering expertise, experimental design methods, statistical analysis, and effective writing and presentation skills. o Provide motivation, coaching and professional development opportunities to the R&D group. o Utilizing strong Program management skills, be capable to take a leadership role o Work closely with marketing in the identification of opportunities for new technologies. o Collaborate with our physician partners to identify novel new technology, improvements to existing product designs or new clinical applications for our current technology. o Develop functional expertise within R&D related to product development processes. o Ensure all design control procedures and company procedures are followed before and during product release. o Conduct or contribute substantially to Design Reviews, Phase reviews, and peer reviews for projects within R&D. o Maintain current knowledge of competitive technologies in addition to medical, technical, and biomedical developments related to products. o Participate, along with project leads, in the development and management of project budgets. o Contribute to the intellectual property position of the company by actively promoting the generation of invention disclosures and patent applications o Maintain a professional and credible image with physicians, consultants, vendors and co-workers. Requirements: Third Level Degree in Engineering (Mechanical, Biomedical, Materials) or equivalent is required. Post Graduate qualification is desirable. 8+ years of relevant experience Good Manufacturing Practices (GMP)/Quality System Regulations (QSR) knowledge For immediate consideration apply online now. If you would like further information before applying please contact: Eamonn O’Raghallaigh MSc on +353 1 685 4848 Your details will not be passed to a Third Party without your express Prior Consent. View our Privacy Policy http://www.newscientistjobs.com/jobs/job/application-scientist-lcms-emea-nuremberg-200644969.htmFri, 20 Nov 2009 13:09:19 +0000194603PreSales Application Scientist – LC/MS Europe, Middle East & Africa (EMEA) Location: Waldbronn, Germany ROLE DESCRIPTION The EMEA Field Support Center is a multicultural work environment with several business functions working intimately with sales channels and customers to achieve to Agilent’s business goals. In our demonstration labs in Manchester, Paris and Karlsruhe we showcase our analytical instrument portfolio to customers and our team of application scientists is leading scientific expertise in the Agilent organization. We are seeking an enthusiastic, people-oriented PreSales Application Scientist to perform sample measurements and customer demos on our high-end LC/MS instruments in intimate collaboration with the LCMS sales organization across EMEA. In addition you will support select marketing activities and interact with our LCMS R&D unit in Santa Clara to address current technologies / applications and to incorporate EMEA requirements into upcoming products. There will be a requirement to: • Team up with the LCMS sales team to close competitive deals by providing customer demonstrations for applications through operating Agilent´s LC/MS instruments and solutions (TOF, QQQ, and QTOF mass analyzers) across a range of small and/or large molecule applications. • Provide post sales technical expertise in conjunction with Agilent’s support team to maintain high levels of customer satisfaction and position Agilent as a leader in Mass Spec. • Deliver customer training classes and specific one-to-one consulting related to the customer’s application. • Maintain and expand critical domain knowledge including latest scientific findings, market & technology trends, industry benchmarks & regulations, competitive positioning. • Participate in the design and delivery of sales trainings, customer workshops and scientific events (e.g. as speaker during conferences, seminars) in close collaboration with the EMEA Marketing Managers. • This position reports into the EMEA Presales Support Team Manager. SUCCESS MEASURES • Overall achievement of EMEA sales target for the LC/MS product line • Number of sample measurements / customer demos successfully completed • Number / quality of supported trainings and other field activities COMPETENCIES & EXPERIENCE REQUIRED • Degree (MSc, PhD) in Analytical Chemistry, Chemistry or equivalent. • Hands-on expertise in LC/MS (Ion Trap, TOF, QTOF, QQQ, FT-ICR) • Significant application knowledge in HPLC and/or Capillary Electrophoresis • Up to date knowledge of current competitive landscape in LC/MS instrumentation • Excellent communication and presentation skills (written / oral) and preferable another major European language. Fundamental knowledge in scientific writing. • Ability to deal with time pressure and high workload, show a structured approach to complete your tasks and fundamental project management skills. • Demonstrated teamwork skills, results-orientation and persistence to reach personal goals. • Ability to work across different organizations in a commercial business environment. Sales experience is advantageous. • Willingness for international travel (throughout Europe, occasionally to the US and India) for up to 25% of the time. We are specifically seeking for talents that want to prove their skills & knowledge in a highly challenging and exposed role. For successful candidates there will be sufficient opportunities to develop within Agilent. http://www.newscientistjobs.com/jobs/job/technical-qara-engineer-medical-device-malaysia-200640899.htmFri, 20 Nov 2009 13:08:33 +0000194586Technical QA/RA Engineer - Medical Device Profile Our client is a global multinational Medical Device manufacturer and they are seeking a Technical QA/RA engineer with excellent attention to detail and technical writing ability to join the team as part of a global technical file management audit project. This is a 2 year fixed term contract position with a view to extension. Job Purpose The successful candidate will develop specifications and inspection criteria, create and update the QA documentations and instructions in line with the Medical Devices Directive and ensure the company is positioned at all times as a key preferred supplier within the medical device space. Key Responsibilities: Apply technical solutions to problem solving Apply technical solutions to quality improvement projects Use technical writing skills to clearly describe technical information Analyze customer complaints, identify trends and execute corrective actions Understand standards and their application to medical devices Planning, protocol generation, testing and report generation for medical devices Generation and maintenance of technical files for medical devices Review and update technical files in line with EU medical devices regulatory requirements The use of GHTF STED format and harmonised standards when compiling a technical file in compliance with the MDD Ensuring that records are filed in accordance with site procedures Supporting R&D Essential Skills / Experience Engineering / Science qualification 3/4 years experience within R&D / QA/ RA/ Compliance or Validation function in a Medical Device Environment Excellent technical writing experience within a medical device environment 2/3 years experience in Risk, Clinical and Biocompatibility an advantage Good knowledge of the Medical Device Directive. Attention to detail and accuracy Ability to work well under deadlines and pressure Problem solving skills for developing creative solutions and meeting objectives are required. Skills that enable coordination of data, including MS-Office (primarily PowerPoint, Word, MD Project, Outlook and Excel); Excellent analytical ability The ability to prioritize tasks and be able to manage several projects and tasks simultaneously; and the ability to interface with all levels of management. Behaviours and Values Approachable, enthusiastic, flexible and adaptable. Ability and Willingness to Travel to Europe and Far East Ability to work on own initiative, self starter and team player Good organisational skills and cultural awareness and sensitivity Good judgement and problem solving ability For Immediate Consideration Please Apply Online Now Or contact for further details: Eamonn O’Raghallaigh on 01 6854848 Life Science Recruitment | http://lifescience.ie Life Science Recruitment is Ireland's foremost specialist scientific and healthcare recruitment agency. We specialize in scientific, pharmaceutical, biotechnology, chemistry, quality management, clinical research, sales and marketing, medical, allied healthcare, regulatory affairs, engineering, pharmacy and research jobs in Ireland. http://www.newscientistjobs.com/jobs/job/technology-acceleration-manager-offshore-renewables-london-london-200644762.htmFri, 20 Nov 2009 10:58:16 +0000194225Technology Acceleration Manager - Offshore Renewables, London, circa £45k This is an exciting opportunity for a candidate with significant commercial, project / programme management experience to participate in a programme of large scale Research, Development and Demonstration activities in offshore wind and marine energy technologies. The role will be based in London based organisation that is at the forefront in creating a low carbon economy. Working for a London based organisation that is at the forefront in creating a low carbon economy, the role of Technology Acceleration Manager - Offshore Renewables(TAM-OR) operates across the portfolio of offshore renewables programmes that are currently running. These are: - The Offshore Wind Accelerator (OWA), a unique co-funding initiative set up to reduce the costs of energy from offshore wind in the short to medium term - The Marine Energy Accelerator (MEA), seeking to deliver a step-change in the cost of energy from wave and tidal stream devices through three complementary strands of innovation - The Marine Renewables Proving Fund (MRPF), supporting the leading wave and tidal stream developers to deploy their full scale devices in the marine environment. The TAM-OR undertakes specific interventions across the three programmes, bringing technical and commercial expertise into the programmes and increasing the capability of the team. Main Duties and Responsibilities will include: - Supporting the delivery of a number of complex and large scale technology innovation projects by co-ordinating contractors and internal teams, and where relevant, co-funders. - Ensure the effective coordination, communication and dissemination of project plans and project end results/products. - Increase knowledge within the organisation of low carbon technologies and sectors - Help develop and deliver technology, policy and market insights - Develop internal papers and business cases for Investment Committees - Feed into business development in terms of ideas generation and evaluation Qualifications and Experience Required: - Significant commercial, engineering or project management experience, including exposure to senior management, at an engineering, manufacturing or technology related business, or a high-end engineering consultancy. - Degree educated (2.1 or above) or MSc or PhD in a science / engineering discipline. - Experience in utility-scale wind energy, including offshore projects or marine energy in the UK (desirable). - Experience of the energy sector (in particular offshore oil and gas), energy efficiency and low carbon technologies (desirable). Salary - circa £45k + bonus & benefits http://www.newscientistjobs.com/jobs/job/research-and-development-engineer-medical-device-republic-of-ireland-200642742.htmFri, 20 Nov 2009 10:52:55 +0000194349R&D Engineer Requirements -Work from basic clinical need to device concept to prototype -Will interface with physicians and distill their needs into product requirements and concepts -May lead a small design team and develop design development path to achieve project goals, alternatively may work largely alone to develop concepts and prototypes -Will apply knowledge of materials and processes to come up with working designs -May be required to progress a project from concept phase into commercialization phase and play a key role there on the product / process / engineering / leadership fronts -Will need to interface effectively with team members and other staff, both in plant and abroad, to achieve goals. REQUIREMENTS: *Qualified to degree level in engineering, science or related discipline *Medical device development experience *Strong design skills *Proven track record in innovative product design, development and implementation For immediate consideration please apply online now. Or for further information please contact Eamonn O'Raghallaigh on 01 685 48 48. http://www.newscientistjobs.com/jobs/job/quality-engineeer-medical-device-republic-of-ireland-200642751.htmFri, 20 Nov 2009 10:52:37 +0000194329Quality Engineer REQUIREMENTS -Evaluation of Customer complaints and co-coordinating the identification of adequate CAPAs -Work closely with Operations to resolve in-house and supplier quality problems using established problem solving methodologies (Root Cause Analysis, Mistake-Proofing, etc). -Actively participate on new product development teams to support product and process design and development activities. -Participate in the development and improvement of the manufacturing processes for existing and new products. -Review and approve inspection plans, routers and product drawings and Operation specifications -Interface with Suppliers for new processes, quality issues and process improvements for assigned projects. -Review/approve nonconforming material and system documentation. -Review/approve product and process change control documentation and specifications. -Providing training to manufacturing personnel on Quality related procedures. -Preparing Quality data as required. -Participate in multi-functional teams set up to drive Quality. -Lead and participate in cross-functional and cross-divisional process improvement initiatives. -Assist in development, review and approval of process and equipment validation/qualifications (IQ / OQ / PQ). REQUIREMENTS: -A degree in an Engineering or Quality discipline. -At least two years industrial experience in a Quality related role. -Excellent communication skills. http://www.newscientistjobs.com/jobs/job/engineering-doctorates-birmingham-birmingham-200643690.htmThu, 19 Nov 2009 11:14:24 +0000191972Engineering Doctorates - Birmingham Engineering Doctorates available at The Centre for Formulation Engineering in the School of Chemical Engineering. Starting tax free bursaries of £19,800 p.a. plus fees paid by the EPSRC. A four year postgraduate qualification carrying out industrially relevant research. Based in a sponsoring company not in the University. Includes taught modules in science, engineering, team building as well as business and management. Complimentary lap top Open to UK / certain EU nationals with a good first degree (upper second or better) in any relevant physical science or engineering discipline. Existing employees with relevant industrial work experience may also be considered. Projects available with; Cadburys (Birmingham) optimization of chocolate refiners MAST Carbon (Guildford) Carbon filter processing for environmental applications Morganite (Corby) Disposable ceramic cores for investment casting Procter & Gamble (Newcastle) Reliability losses in transfer and packing Rich Foods (USA) Use of protein coated air cells in whipped emulsions Rolls -Royce (Derby) Disposable ceramic cores for turbine blade manufacture Unilever (Netherlands) modeling and validation of thermal processes For more details on each project please see our website. • If you meet the EPSRC entry requirements please e mail your c.v. via the ‘Apply Now’ button. A University of Fairness and Diversity. POSITIVE ABOUT DISABLED PEOPLE http://www.newscientistjobs.com/jobs/job/chair-in-sustainable-technologies-reading-reading-200643688.htmThu, 19 Nov 2009 11:14:22 +0000191970Chair in Sustainable Technologies - Reading School of Construction Management and Engineering This appointment is full-time, permanent We are looking for a senior academic to lead the further expansion of research and teaching within the broadly defined field of sustainable technologies for the built environment. This new Chair will provide leadership in further developing our inter-disciplinary approach to sustainable technology, with particular emphasis on collaborative research. The appointee will become Director of the Centre for Technologies for Sustainable Built Environments (TSBE). You will have: the ability to provide academic leadership, especially in research initiation and management successful supervision and management of research projects broad knowledge of energy and engineering design issues experience of industry-orientated research in the UK context orientation towards inter-disciplinary research established publication record and international reputation Experienced candidates will be provided with the support necessary to grow a vibrant and enthusiastic team. Informal enquiries: contact the Head of School of Construction Management and Engineering, Professor Will Hughes on +44(0)118 378 7175 or email w.p.hughes@reading.ac.uk Alternatively contact the Deputy School Director of Research, Dr Jennifer Whyte on +44(0)118 378 5228 or email j.whyte@reading.ac.uk Closing date: 8 January 2010 To formally apply please visit our website or contact Human Resources, University of Reading, Whiteknights, PO Box 217, Reading RG6 6AH. Telephone +44(0)118 378 6771 (voicemail) Please quote reference number CH09012 We value a diverse workforce and welcome applications from all sections of the community http://www.newscientistjobs.com/jobs/job/lecturer-in-structural-mechanics-and-structural-materials-newcastle-newcastle-200643684.htmThu, 19 Nov 2009 11:14:19 +0000191968Lecturer in Structural Mechanics and Structural Materials - Newcastle School of Civil Engineering & Geosciences Ref: G445 This post will be based in the growing Geotechnical Engineering and Structures (GEST) Group. The Lecturer will be developing a successful research profile in areas consistent with the Group's focus. You will also contribute to undergraduate and postgraduate taught programmes, and project supervision at undergraduate and MSc levels. For an informal discussion about this post please contact either Head of School, Professor David Parker, tel: (0191) 222 6447/e-mail: david.parker@ncl.ac.uk or Professor Peter Gosling tel: (0191) 222 6422/e-mail: p.d.gosling@ncl.ac.uk Please apply on line at our website. Closing date: 11 December 2009 Committed to Equal Opportunities