Jobs in Science in Cambridgeshire

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Susan Hamilton Group (26)
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The One Group (1)

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Medical Writer - Medical Communications - Cambridgeshire - Cam
Medical Writer - Medical Communications - Cambridgeshire - Cambridge A highly reputable medical communications agency has a new opening for a Medical Writer to join their expanding team based in their Cambridge office. Providing leading marketing, consultancy and communications services to the Pharmaceutical Industry this is an excellent opportunity to further your career in a driven and committed agency. As a Medical Writer you will be involved in writing up conferences and advisory boards, working with researchers on primary research publications, commissioning and editing material for publications and write articles for in house journals. . The successful candidate will ideally have a strong science background with a life science degree. Experience within a Medical Communications Agency is not essential however candidates with experience in the pharmaceutical and publishing sector will have a clear advantage. You will also be a team player and have good communication skills. In return you will enjoy an excellent salary and benefits package. This agency is well known for its friendly working environment and its exciting, fast-paced atmosphere is echoed in the work produced. Medical writer, medical editor, editorial assistant, medical communications, medical publishing, medical education, healthcare communications, scientific publishing 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.

Thu, 21 Aug 2008 14:49:27 GMT

In Vitro Analyst- Cambridgeshire
In Vitro Analyst- Cambridgeshire Exciting opportunity for an experienced scientist within In Vitro metabolism! Working closely with study directors you will be responsible for performing in vitro assays in the study of human metabolism and metabolic reactions to drug candidates. You must have a minimum of 12 months experience (or equivalent) performing assays such as cytochrome P450, Caco2 permeability, hERG, and immunoassays, ideally from within a GLP environment. This is the ideal role for an experienced analyst looking to progress their career in a successful and rapidly expanding laboratory!

Thu, 21 Aug 2008 11:52:26 GMT

Biotechnology - Senior Manager Drug Safety Jobs - Cambridge (UK)
Flame Pharma Biotechnology - Senior Manager Drug Safety Job - Cambridge (UK): Cambridge, UK: Salary up to ?60k Flame Pharma is working alongside a global bio-pharmaceutical organisation at the forefront of developing new medicines in areas where the need is currently unmet. This pioneering company has an impressive portfolio of products in anti-viral, cardiovascular and respiratory therapeutic areas. As a result of expansion within their offices in Cambridge, UK, we are working on a recruitment project to source a Senior Manager within Drug Safety to be responsible for safety evaluation work for specified products. The Role Working within a highly respected drug safety team, the Senior Manager Drug Safety will be responsible for Evaluation & Risk Management for Drug Safety & Public Health issues. You will have a proactive management of potential safety issues and provide risk management plans and responses to regulatory agency safety enquiries. You will collaborate closely with the drug safety physician responsible for the specified product and liaise with partner companies on safety evaluation for co-licensed products. The Senior Manager Drug Safety will participate in safety committee meetings (internal or with partner companies) and takes the lead for assigned projects and is fully responsible for all activities relating to them. The Person The Senior Manager Drug Safety must have a scientific degree, and have proven, extensive drug safety evaluation and risk management experience. You will have a well developed scientific and analytical knowledge base, with an in depth understanding of good pharmacovigilance practices and current drug safety regulations. Key Words Senior Manager Drug Safety, Drug Safety, Pharmacovigilance, PV, Regulatory Affairs, Medical Affairs, Pharmacovigilance, Drug Safety, Clinical Research, Clinical Trials, Medical, Clinical, CRO, Study Management, Clinical Management, Pharmaceutical, Career, Research, Cambridge For further information about this role, please contact Flame Pharma.

Thu, 21 Aug 2008 11:19:07 GMT

Biotechnology - Clinical Program Manager - Cambridgshire
Flame Pharma Biotechnology - Clinical Program Manager Job - Cambridgshire UK: Salary up to ?50,000. Car allowance of ?7,980. Stock options 12%. Bonus (not guaranteed). 7% pension contributions. BUPA Healthcare. 25 days holiday plus bank holidays. Life cover 4 x annual salary. Employee Share Scheme Flame Pharma is working alongside a global Bio-Pharma that discovers, develops and commercializes innovative medicines in areas of unmet need in their search for an experienced Clinical Program Manager. This career building role will be based at their state of the art site in Cambridgshire. The Role Reporting to the Head of Program Management you will manage clinical trials within designated program budgets and timelines & provide leadership and therapeutic expertise for the successful management of national clinical trials. Within this role you will develop RFPs, set up and management of external vendors along with providing direction for CRA and CPA in study team. You will participate in development of SOPs, Clinical Study Reports and other cl inical, regulatory, safety documents & Contribute to development of abstracts, presentations, and manuscripts. You will be required to solve problems and use judgment referring to national regulations, guidelines, investigator interactions and timelines. The Person You will be a Clinical project Manager with the ability to successfully develop, implement, manage and complete clinical trials to budget and timelines, have direct experience in management of external resources and vendor relations, writing study protocols with little supervision & excellent communication and presentation skills. You will have direct analytical skills with strong customer (internal & external) orientation & the ability to lead cross-functional teams and mentor junior staff. You will have a Bsc in life sciences with broad experience in pharmaceutical industry, extensive experience of clinical trial process, direct industry UK project Management experience, extensive knowledge of ICH GCP, national regulations & associated EU Directives. Key Words Clinical Program manager, Clinical Project Manager, Pharmacovigilance, Drug Safety, Director, Manager, Management, Clinical Research, Clinical Trials, Medical, Clinical, CRO, Study Management, Clinical Management, Pharmaceutical, Career, Research, Cambridgshire, Job, Recruitment For further information on this vacancy, please contact Flame Pharma.

Thu, 21 Aug 2008 11:19:07 GMT

Biotechnology ? Associate Manager, Drug Safety Jobs - Cambridgeshire
Flame Pharma Biotechnology - Associate Manager, Drug Safety Job - Cambridgeshire: Job Summary This leading research based biopharmaceutical company is looking to recruit an associate manager within Drug safety to work in their leading Cambridgeshire site. This Fantastic position has an excellent salary of circa ?40K!. If you are looking for an opportunity to demonstrate your skills and experience, then this leading position is for you! Job Title Associate Manager Drug safety Background Due to expansion, our client is looking to recruit an associate manager, within Drug safety who has team leader or supervision experience to be able to cover in times of absence of the manager. You will have presentation and project management experience. Good communication skills, both verbally and written and excellent attention to detail. You must be up to speed with current EU legislation and be proficient in excel, powerpoint, word and be experienced with using databases. Data entry work is required. The right person must be a team player. Key Responsibilities - Independently establishes work priorities and direction with minimal input from Manager - Acts as a trainer and mentor for more junior global drug safety staff - Takes responsibility for (a) specific project(s),with minimal direction and input from their manager - Provide training on the principles and practises of drug safety to personnel or to external groups - Recognises potential or impending problems and implements solutions - Seeks assistance from appropriate internal and external resources - May receive and review adverse event forms for completeness, recognises discrepancies, enters data into serious adverse event database, solicits follow-up information and assesses causal relationship of event to drug - May work with Clinical Research and Contract Research Organisations, sometimes in a lead capacity, regarding information exchange and safety exchange agreements Qualifications and Experience - Ability to maintain confidentiality (especially on patient records), for quality and accuracy - Demonstrates attention to detail, teamwork and initiative. Ability to mentor and coach. - Must be proficient in email and verbal communication. - Must have a full working understanding of current regulations within drug safety. - Previous experience and understanding of a drug safety database is required. - Must be proficient in Microsoft Excel, Power point and Word. - This role requires a BS degree in life sciences, pharmacy, nursing - Relevant experience, which includes drug safety Benefits With this position comes an attractive benefits package that you associate with a world leader, including: - Basic salary circa ?40k - Stock options of 650 - Bonus 9% (not guaranteed) - Holidays 25 days plus 8 bank holidays - BUPA healthcare - Company pension contributions of 7% annual salary - Life Insurance 4 x annual salary - Employee Stock Purchase Plan Key Words Drug safety, associate manager, Clinical Research, Clinical Trials, Medical, Clinical, CRO, Study Management, Clinical Management, Pharmaceutical, Career, Research This vacancy will be based in Cambridge For further information on this vacancy, please contact Flame Pharma.

Thu, 21 Aug 2008 11:19:07 GMT

Medical Devices - Compliance Officer Jobs - Cambridgeshire
Flame Pharma - Medical Devices - Compliance Officer Job - Cambridgeshire JOB SUMMARY: Salary: Up to ?30K Flame Pharma is working alongside a leading Global Medical Devices Organisation to appoint an experienced Compliance Officer to join their focused and dedicated team in their state of the art facilities in Cambridgeshire. This new and exciting opportunity will enable this rapidly growing, dynamic and entrepreneurial organisation to maintain their unwavering focus on producing leading edge products and moving technology forward. This exceptional opportunity will require the very best within the Medical Devices sector and as a result, the salary, benefits package and autonomous working environment are reflective of this. THE ROLE: You will ensure continuing compliance in accordance with ISO13485, FDA 21 CFR 820 and other Quality Management System requirements. Measuring, analysing and reporting any KPI data generated from core Quality Management Systems processes. You will be responsible for the development and optimisation of the Quality Management Systems processes in response to changing business and regulatory requirements. THE PERSON: You will have proven medical device industry experience, preferably within a Quality Management Systems or GMP environment and be educated to degree level or an equivalent qualification. You must have a flexible working approach together with a desire to succeed. Experience with formal testing procedures is desirable, and should include the use of high-precision test equipment. Excellent numerical and literacy skills are required, as is a high level of accuracy and attention to detail. You must possess the ability to communicate at all levels within the organisation together with the ability to work as both part of a team or on your own initiative where required. In addition you should be an experienced internal auditor with training to ISO 9001 or similar. KEY WORDS: Compliance Officer, Clinical Research, Clinical Trials, Medical, Clinical, CRO, Study Management, Clinical Management, Pharmaceutical, Career, Research, Job, Recruitment, Cambridgeshire. For further information on this vacancy please contact Flame Pharma.

Thu, 21 Aug 2008 11:19:07 GMT

Pharmaceutical - Development Scientist Jobs- Cambridgeshire
Flame Health Pharmaceutical - Development Scientist Job - Cambridgeshire Salary: Negotiable Flame Pharma is working alongside a leading Clinical Research Organisation to appoint a dedicated and enthusiastic Development Scientist. This forward thinking, dynamic organisation are offering the ideal candidate this unique opportunity to join their team orientated, friendly and enjoyable working environment in their modern state of the art facilities in Cambridgeshire. Due to expansion, this new and exciting opportunity will enable this established organisation to maintain their unwavering focus on contributing to the development of important therapies. This role will require the very best within the Clinical Research sector and as a result, the salary and benefits package are reflective of this. Teamwork and commitment will be rewarded and you will receive the full training and support to reach your potential. THE ROLE: As a Development Scientist within the Clinical Sciences Department you will provide scientific input into bio-marker-based research, to include developing assays applicable to the needs of the Bio-marker and Clinical Laboratories. It will be your responsibility to develop, validate and perform laboratory assays to agreed standards, interpreting any scientific data and reaching conclusions regarding its relevance. In addition, you will train and mentor staff carrying out validation work and routine analysis. You will analyse and resolve any problems that occur during assay development, validation or routine analysis, participating in the validation of equipment as necessary. You may be required to take on the role and responsibilities of Study Director in relevant clinical or laboratory-only studies. THE PERSON: You will be educated to at least degree level, in a scientific discipline with extensive proven experience in a drug discovery/development environment. A strong background in assay validation and development is essential as is experience of Immunoassay techniques and flow cytometry. The role also requires a strong background in bioscience. KEY WORDS: Development Scientist, Clinical Research, Clinical Trials, Medical, Clinical, CRO, Study Management, Clinical Management, Pharmaceutical, Career, Research, Cambridgeshire, Recruitment

Thu, 21 Aug 2008 11:19:07 GMT

Thu, 21 Aug 2008 11:12:17 GMT

Thu, 21 Aug 2008 11:10:21 GMT

Thu, 21 Aug 2008 11:08:24 GMT

Technical Assistant - IJP
60;strong62;Job Description60;47;strong62;60;br 47;62;60;br 47;62;My client is currently recruiting for a Technical Assistant to provide skilled support to the ink jet printing process development team assisting with the development of ink jet printing processes and metrology.160;60;br 47;62;60;br 47;62;This will involve handling fluids and fine chemicals, surface preparation of substrates and the160;operation of ink jet print process equipment.160;60;br 47;62;60;br 47;62;You will ideally have a deg ...

Thu, 21 Aug 2008 10:45:13 GMT

In Vitro Analyst
Exciting opportunity for an experienced scientist within In Vitro metabolism! Working closely with study directors you will be responsible for performing in vitro assays in the study of human metabolism and metabolic reactions to drug candidates. You must have a minimum of 12 months experience (or eq ...

Wed, 20 Aug 2008 22:00:00 GMT

Analyst - Organic Chemistry
Our client provide services to the environmental industry. They are looking for someone to join their organic chemistry department on a temp to perm basis. The purpose of the role is to generate and interpret results on organic analytical tests. This^will involve sample preparation, interpretation of chromato ...

Wed, 20 Aug 2008 22:00:00 GMT

Atomic Absorption Applications Chemist
Do you have Atomic Absorption experience? Are you looking for a challenging and diverse new position? Our client has an exciting opening for an Applications Chemist. You will collaborate with other scientific organisations to develop new methods, deliver training and demonstrate instrumentation. The ...

Wed, 20 Aug 2008 22:00:00 GMT

GMP 47; GCP QA Manager
A rare opportunity for an experienced QA 47; Quality Assurance professional to take responsibility for the GMP and GCP QA function at a leading clinical research organisation. You will assume responsibility for the day to day management of the department and a team of GMP and GCP Auditors 8211; an excellent opportunity.60;br 47;62;60;br 47;62;60;strong62;QA 47; Quality Assurance Manager 8211; GMP47;GCP60;br 47;62;East Anglia60;br 47;62;163;40,000 region 43; excellent bens60;br 47;62;60;47;strong62;60;br 47; ...

Wed, 20 Aug 2008 16:35:33 GMT

Scientific Operations Manager
Excellent opportunity for an experienced Scientific Manager to take a senior management role within the QA group of a large R38;amp59;D centre. With responsibility for the operation of the GLP QA function and working closely with your team leaders, your will build, lead and motivate the department to meet the needs and aims of the organisation.160;60;br 47;62;60;br 47;62;60;strong62;Scientific Operations Manager60;br 47;62;Cambridgeshire60;br 47;62;163;40,000 43; excellent benefits60;br ...

Wed, 20 Aug 2008 16:33:16 GMT

Wed, 20 Aug 2008 16:31:53 GMT

Wed, 20 Aug 2008 16:30:26 GMT

Research Scientist
AKCDT 12444 Research Scientist · Cambridge · Permanent · 25-35K We are currently seeking a Research Scientist to work for our client, a large Biotechnology company in Cambridge. Working within the Formulation Team, you will provide formulation, analytical and drug delivery support to Pre-formulation and pharmaceutical delivery activities. Duties: · Conduct Pre-formulation/formulation studies (lyophilization/freeze drying and liquid formulations). · Conduct drug delivery and device evaluation on pre-filled and autoinjector devices. · Coordinate stability studies on liquid and freeze dry formulations. · Support external academic collaborations · Write protocols, documents and procedures in support of formulation analysis. Requirements: · PhD Biological Sciences/Biochemical Engineering · Proven Industrial experience in lyophilisation, drug delivery and protein analytical components. · Practical experience in the following techniques: SDS PAGE, Isoelectric focussing, HPLC, UV-vis spectrophotometry, ELISA. · Computer literate. · Good communication, both verbal and written · Ability to plan and organise work with minimal supervision. Interested in this fantastic opportunity? Please apply on-line or contact Alana Kilkenny for more information on: 0161 868 2205; alana.kilkenny@srg.co.uk The recruiter has stated that all applicants for this job should be able to prove that they are legally entitled to work in the UK. Carlisle Staffing plc, trading as SRG is an Employment Business/Agency. SRG winners of the 2008 Recruiter Awards for Excellence: Best Candidate Care and Best Health Care/Medical Recruitment Firm.

Wed, 20 Aug 2008 14:36:21 GMT

Laboratory Assistant
PULSE Scientific are representing an exceptional organisation based on the Herts47; Cambs border. Due to an internal restructure, the position of Laboratory Assistant has arisen within this internationally renowned business.38;lt59;br 47;38;gt59;38;lt59;br 47;38;gt59;Reporting in to the Laboratory Manager, your role will have the following responsibilities58;38;lt59;br 47;38;gt59;38;lt59;br 47;38;gt59;To prepare and despatch samples38;lt59;br 47;38;gt59;To source samples from finished stock38;lt59;br ...

Wed, 20 Aug 2008 13:29:12 GMT

Atmospheric Scientist/Mathematical Modeller ? Cambridge
We are seeking applications from graduates or post-graduates of high ability in applied maths, physics or engineering to join our team in Cambridge. CERC develops, supports and promotes environmental software that is used in commercial and research applications worldwide. For example: - Current projects include analysis of flows around wind turbines and anthropogenic heat island effects. - We have recently launched a new model, ADMS-Airport, used to model air quality in and around airports. - Our air quality forecasting and alert services help the public avoid high pollution episodes. www.airtext.info The work is both intellectually challenging and driven by commercial considerations so we are looking for people capable of finishing tasks within deadlines. Required attributes: ? proven high ability in mathematics, physics or engineering ? knowledge of some or all of the following: meteorology, atmospheric sciences, aeronautics, CFD, meso-scale atmospheric modelling, wind engineering. ? ability to communicate effectively in written and spoken English Desirable attributes & skills: ? experience of programming e.g. some of the following: FORTRAN, MATLAB, SQL, PHP. Permanent and temporary positions are available. If you would like to join us please email or write sending your CV and a covering letter telling us why you are interested in joining CERC to: Angela Manlow, CERC, 3 Kings Parade, Cambridge, CB2 1SJ. Tel No. 01223 357773 E-mail via the 'Apply Now' button below. Applications must be received by 25 September 2008

Wed, 20 Aug 2008 09:18:08 GMT

Development Scientist - Cambridge, UK
Abcam is a rapidly growing business, specialising in the production and sale of antibodies and related products. We are a web-based business, with offices in Cambridge, UK, Cambridge, USA and Tokyo, Japan. To support our continued expansion, we are looking for a Development Scientist to take a key role within our Product Development and Manufacture facility. Working within the Characterisation Team, the Development Scientist will be responsible for developing lab processes, ensuring Abcam?s customers receive high quality in-house products and experience good service. The Development Scientist will also characterise antibodies using Western Blot techniques, produce good quality data which they can then interpret and analyse. As part of the role you will be required to work with Business Development to discuss problems and ideas concerning testing conditions and flag any products where there are any quality concerns. You will be educated to degree level in biological sciences or equivalent. Candidates will need to have previous lab experience along with experience of Western Blot techniques, any experience of other antibody characterisation techniques would be an advantage. Candidates also need to have good problem solving skills, be organised, enthusiastic and a good team player. In addition to competitive salaries we can offer an attractive flexible benefits package which includes a profit-share scheme and share options. To apply please send a CV and covering letter (together with your current salary) to Bonnie Anderson: bonnie.anderson@abcam.com. As part of the application process you should go to our website www.abcam.com/careers and complete the Diversity Information form and return it with your CV. Closing Date: 19th September 2008

Wed, 20 Aug 2008 08:15:07 GMT

Senior Cell Culture Manager
Ref: PDM082 Abcam is a rapidly growing business, specializing in the production and sale of antibodies and related products. We are a web-based business, with offices in Cambridge, UK, Cambridge, USA and Tokyo, Japan. Abcam has recently undertaken a major expansion of its Laboratory and Production capabilities with a brand new facility that opened in June 2007. The laboratories occupy 20,000 square feet on the Cambridge Science Park, Cambridge UK. The cell culture group is a major contributor to the continuing success of Abcam?s multi-million pound investment in Product Development & Manufacture. You will play a pivotal role in managing the growth and development of the cell culture facility to support future strategic objectives. You will be an active member of the Product Development & Manufacture Management team. You will be responsible for managing, leading and developing the cell-culture group. In addition, you will develop processes & procedures and ensure that production targets for monoclonal antibody development, hybridoma production and for cell-culture services are consistently met. You will innovate within the area of cell-culture to continually improve the processes and productivity, with full involvement of the team members. Part of your initial challenge will be to manage the successful integration of cell-culture automation. You will also be responsible for setting and implementing routine mycoplasma contamination testing and disaster recovery policies. You will be educated to degree level in biological sciences and have extensive mammalian cell-culture experience including scaling cell culture systems and cell-line development. Experience in hybridoma development and selection will be an advantage. You will have experience of managing teams and motivating those teams to consistently meet production targets. You will have good IT skills and have experience of preparing and reporting KPIs. You will have demonstrated the ability to deliver successful research or process development projects. Candidates also need to have good problem solving skills, be organized, enthusiastic and a good team player. At Abcam we require brilliant individuals who will work hard to deliver great service and the best products to our customers. In return Abcam can provide the opportunity for you to focus on and develop your career, inspire and influence the environment around you along with being rewarded for your great contribution. In addition to competitive salaries we offer an attractive flexible benefits package which includes a profit-share scheme and share options. To apply please send a CV and covering letter (together with your current salary) to Bonnie Anderson via the 'Apply Now' button below. As part of the application process you should go to our website www.abcam.com/careers and complete the Diversity Information form and return it with your CV.

Wed, 20 Aug 2008 08:12:21 GMT

Business Development Manager Bioinformatics & Expert Systems ? Cambridge, UK
Ref: BD015 Abcam is a rapidly growing business, specialising in the production and sale of antibodies and associated products. We are a web-based business, with offices in Cambridge, UK, Cambridge, USA and Tokyo, Japan. To support our continued expansion we are looking for a Business Development Manager to support the ongoing development of our bioinformatics and expert systems. You will be responsible for the optimisation of these systems to enhance the commercial production of antibodies together with using data mining technologies to ensure understanding of product catalogue content, and customer sales behaviours. The ideal candidate will have a laboratory based PhD in Biomolecular Sciences with practical experience of using scientific protocols incorporating antibodies. Bioinformatics/molecular informatics experience is essential together with excellent collaborative skills and advanced skills in data analysis and manipulation. Working knowledge of workflow technologies (e.g. Taverna), data mining tools (e.g. Weka), visualisation and knowledge modeling tools (e.g. Prot?g?) will be a strong advantage, as will be a thorough knowledge and experience with all major protein information databases (e.g. Swissprot). In addition to competitive salaries we can offer an attractive flexible benefits package, profit-share scheme and share options. To apply for the position please send a CV and covering letter (together with your current salary) to Bonnie Anderson via the 'Apply Now' button below, as part of the application process you should go to our website www.abcam.com/careers and complete the Diversity Information form and return it with your CV. Closing date for applications: Monday 1st September, 2008

Wed, 20 Aug 2008 08:05:59 GMT

QA / Quality Assurance Manager - GMP/GCP
A rare opportunity for an experienced QA / Quality Assurance professional to take responsibility for the GMP and GCP QA function at a leading clinical research organisation. You will assume responsibility for the day to day management of the department and a team of GMP and GCP Auditors ? an excellent opportunity. QA ...

Tue, 19 Aug 2008 22:00:00 GMT

Scientific Operations Manager
Excellent opportunity for an experienced Scientific Manager to take a senior management role within the QA group of a large R&D centre. With responsibility for the operation of the GLP QA function and working closely with your team leaders, your will build, lead and motivate the department to meet the needs and aims of th ...

Tue, 19 Aug 2008 22:00:00 GMT

Analytical Team Leader - Cambridgeshire - 30-35K
Analytical Team Leader - Cambridgeshire - 30-35K My client is a leading contract research organisation (CRO) based in Cambridgeshire. They are currently recruiting a Team Leader for their Biopharmaceutical Analysis group. The group provides characterisation, stability testing and batch release services, together with dev ...

Tue, 19 Aug 2008 22:00:00 GMT

PCR Development Scientist - Cambridgeshire to 25k
PCR Development Scientist (Study Analyst) - Cambridgeshire to 25k My client is a leading contract research organisation based in Cambridgeshire. They are a world famous organisation and currently are recruiting a number of experienced PCR assay development scientists. The role consists of designing, developing and validat ...

Tue, 19 Aug 2008 22:00:00 GMT

Metabolism Study Scientist - Cambridgeshire - 18-20K
Metabolism Study Scientist - Cambridgeshire - 18-20K Based in Cambridgeshire a fantastic opportunity has arisen for a Metabolism scientist to work with a leading CRO. If you have a relevant degree and ideally 1 or more years experience in a Metabolism laboratory then this is the role for you. The successful candidate wil ...

Tue, 19 Aug 2008 22:00:00 GMT

Territory Manager
Company: Our client is an International Leader in Genomics. They provide a full range of genomics services for both research and regulated projects, including services to support pharmacogenomics discovery and validation and biomarker research and development. Position: Due to rapid growth, o ...

Tue, 19 Aug 2008 22:00:00 GMT

Qualified Person
The purpose of the role is to act as a Qualified Person and manage the Therapeutics QA activities for the release and distribution of therapeutics products. You will undertake Qualified Person responsibilities as defined in Directive 2001/83/EEC andthe Code of Practice for Qualified Persons of the Institute o ...

Tue, 19 Aug 2008 22:00:00 GMT

Principal Clinical Supply Specialist
I am looking for someone to support the Manager of Clinical Pharmacy Research Services (CPRS) in developing, implementing and running CPRS activities to support EU, US and International sponsored clinical trials. You will provide the packaging and logistical support, and expertise to optimise the design and e ...

Tue, 19 Aug 2008 22:00:00 GMT

Laboratory Assistant
PULSE Scientific are representing an exceptional organisation based on the Herts/ Cambs border. Due to an internal restructure, the position of Laboratory Assistant has arisen within this internationally renowned business. Reporting in to the Laboratory Manager, your role will have the following responsibilities: To prepa ...

Tue, 19 Aug 2008 22:00:00 GMT

Pilot Plant Chemist
I am looking for a chemist to operate a pilot plant in compliance with regulatory requirements to manufacture active pharmaceutical ingredients for clinical and other trials. You will execute routine experimental work, both in the pilot plant and laboratory and support the design, development, scale up and/or ...

Tue, 19 Aug 2008 22:00:00 GMT

Clinical Trial Supplies Technician
You will ensure clinical trial supplies are labelled, packed and dispatched in a timely manner and in accordance with current regulatory requirements and Good Manufacturing Practice Guidelines. Main duties will include the drafting and printing of clinical trial labels, the receipt of clinical trial material ...

Tue, 19 Aug 2008 22:00:00 GMT

Senior Site Chemist - Waste Management
The Senior Chemist is required to supervise the Site Chemists, ensuring the safe, efficient and economical processing of materials through the site in compliance with all relevant SHE legislation and company procedures/policies. Main responsibilities include: Assisting and deputising for the Operations Manage ...

Tue, 19 Aug 2008 22:00:00 GMT

Analytical Chemist - GCMS / ICP
Our client is an Environmental Analytical Consultancy with a laboratory in the Cambridgeshire / Northamptonshire area. They are looking for an Analytical Chemist to come and join them in the testing labs primarily using GCMS and ICP to look for trace^metals and other contaminants in soil and water samples. You must ...

Tue, 19 Aug 2008 22:00:00 GMT

Biopharmaceutical Principal Scientist
Exciting opportunity to lead a team of analysts within a successful and expanding biopharmaceutical laboratory33;60;br 47;62;60;br 47;62;You must have a solid background performing and validating immunoassay based technologies such as SDS-PAGE, ELISA, Western Blot, PCR and HPLC, ideally gained within a GMP environment.60;br 47;62;60;br 47;62;To learn more contact VRS now33;13;10;60;33;-- Sector58; Cambridge Biopharmaceutical Principal Scientist VRS --62; ...

Tue, 19 Aug 2008 14:51:56 GMT

Pharmaceutical Analyst
Working within the biopharmaceutical analysis team you will be involved in the characterisation of biopharmaceutical products. This will involve the application of various techniques including immunoassays, HPLC, determining biological potency and physico-chemical properties. You will be responsible for developing and optimising analytical methods as well as collating data and drafting reports.60;br 47;62;60;br 47;62;You must have at least 18months experien ...

Tue, 19 Aug 2008 14:50:22 GMT

Tue, 19 Aug 2008 14:49:15 GMT

Tue, 19 Aug 2008 14:48:28 GMT

Biopharmaceutical Principal Scientist - Cambridgeshire
Biopharmaceutical Principal Scientist - Cambridgeshire Exciting opportunity to lead a team of analysts within a successful and expanding biopharmaceutical laboratory! You must have a solid background performing and validating immunoassay based technologies such as SDS-PAGE, ELISA, Western Blot, PCR and HPLC, ideally gained within a GMP environment. To learn more contact VRS now!

Tue, 19 Aug 2008 14:03:19 GMT

Pharmaceutical Analyst -Cambridgeshire
Pharmaceutical Analyst -Cambridgeshire Working within the biopharmaceutical analysis team you will be involved in the characterisation of biopharmaceutical products. This will involve the application of various techniques including immunoassays, HPLC, determining biological potency and physico-chemical properties. You will be responsible for developing and optimising analytical methods as well as collating data and drafting reports. You must have at least 18months experience (or equivalent) with a number of these techniques, ideally gained within a GMP regulated environment. To learn more contact VRS now!

Tue, 19 Aug 2008 14:00:49 GMT

Postdoctoral Fellow ? ?Signal transduction in the malaria life cycle? - Ref: 80195 - Cambridge - ?27,450 to ?34.402
The Wellcome Trust Sanger Institute is a world leader in genomic research, with an expanding scientific programme dedicated to understanding gene function in health & disease. The Billker team studies malaria parasites in rodent models to understand fundamental parasite biology and pathogen-host interactions. We also seek new ways of identifying and evaluating targets for drug and vaccine development. The project seeks to identify key molecular pathways and mechanisms regulating the parasite?s complex life cycle, as it alternates between mouse and mosquito (see for instance Cell, It offers the opportunity to combine powerful experimental genetic tools with systematic biochemical approaches such as phosphoproteomics. Essential Skills We are looking for a highly motivated and independent individual, who can demonstrate skills in protein biochemistry and signal transduction research. Other information Postdoctoral Fellows are typically in their first or second postdoctoral position as part of a period of early career research training. This is up to 3 year fixed-term contract. Informal enquiries can be made to Oliver Billker (ob4@sanger.ac.uk). Benefits We offer a comprehensive range of benefits including a final salary pension scheme and excellent on-site facilities. Further details can be found on our website https://jobs.sanger.ac.uk, To submit your CV and apply for this job please go to https://jobs.sanger.ac.uk, to register and apply on line. Closing date: 19th September 2008

Tue, 19 Aug 2008 13:54:48 GMT

Postdoctoral Fellow - ?Identifying mouse genes that modulate malaria? - Ref: 80194 - Cambridge - ?27,450 to ?34,402
The Wellcome Trust Sanger Institute is a world leader in genomic research, with an expanding scientific programme dedicated to understanding gene function in health & disease. The Billker team studies malaria parasites in rodent models to understand fundamental parasite biology and pathogen-host interactions. We also seek new ways of identifying and evaluating targets for drug and vaccine development. We now aim to develop novel cell culture-based assays and rodent infection protocols to access the institute?s large programme in mouse genetics for the experimental identification of host genes that modulate malaria. Essential Skills For this project we are looking for a highly motivated and independent individual, who can demonstrate advanced skills in animal models of disease and cell culture techniques. Ideal Skills Experience in rodent immunology, mouse phenotyping or mouse malaria would be an advantage. Other information Postdoctoral Fellows are typically in their first or second postdoctoral position as part of a period of early career research training. This is up to 3 year fixed-term contract. Informal enquiries can be made to Oliver Billker (ob4@sanger.ac.uk). Benefits We offer a comprehensive range of benefits including a final salary pension scheme and excellent on-site facilities. Further details can be found on our website https://jobs.sanger.ac.uk, To submit your CV and apply for this job please go to https://jobs.sanger.ac.uk, to register and apply on line. Closing date: 19th September 2008

Tue, 19 Aug 2008 13:51:02 GMT

Advanced Research Assistant - Mosquito maintenance and insectary management - Ref 80192 - Cambridge - ?21,115 to ?27,450
The Wellcome Trust Sanger Institute is a world leader in genomic research, with an expanding scientific programme dedicated to understanding gene function in health & disease. The Billker team studies malaria parasites in rodent models to understand fundamental parasite biology and pathogen-host interactions. We also seek new ways of identifying and evaluating targets for drug and vaccine development Essential Skills The successful candidate will provide important research services to other members of the team by maintaining mosquito colonies and mouse malaria parasites throughout their life cycle. The person will also be responsible for independently running a small insectary facility, including ordering supplies, arranging equipment and facility maintenance and repair, monitoring environmental controls and providing technical support to the research team; the ability to follow protocols and implement Health and Safety in the laboratory are essential. Ideal Skills The ideal candidate will have experience of working with insects or animals in a research environment. We are looking for a technically minded person with good organizational skills, who is a strong team player and good communicator, but who can also independently solve problems and prioritize tasks to respond to quickly changing needs. Other information Informal enquiries can be made to Oliver Billker (ob4@sanger.ac.uk). Benefits We offer a comprehensive range of benefits including a final salary pension scheme and excellent on-site facilities. Further details can be found on our website https://jobs.sanger.ac.uk, To submit your CV and apply for this job please go to https://jobs.sanger.ac.uk, to register and apply on line. Closing date: 19th September 2008

Tue, 19 Aug 2008 13:27:45 GMT

Senior Site Chemist
60;strong62;Organisation Description60;47;strong62;60;br 47;62;60;br 47;62;My client is one of the world leaders in environmental services. They are currently recruiting for a Senior Site Chemist for their site in160;Cambridge.160;60;br 47;62;60;br 47;62;The Senior Chemist is required to supervise the Site Chemists, ensuring the safe, efficient and economical processing of materials through the site in compliance with all relevant SHE legislation and company procedures47;policies.60;br 47;62; ...

Tue, 19 Aug 2008 13:05:19 GMT

Senior Renewables (Marine) Consultant
Our client is an international consultancy working across a wide spectrum of areas in a challenging and exciting market place. Our client employees more the 3500 people worldwide and has an impressive reputation in its arena. They are currently looking for a Senior Renewables (Marine) Consultant to provide coastal and marine expertise and advice within the technical group. The position offers enormous opportunities for the successful candidate to develop their own skills and to advance technically. They are looking for a proven scientist who can work well within project and technical teams (including fostering the development of younger staff) and who is able to individually develop their own leads and promote rewarding business development. Responsibilities will include: *Contribution to project work (UK and overseas), includes report writing, field work supervision, organisation, consultation and project management. *Manage complex projects *Remaining up to date with policy and legislative developments in a range of sectors. *Presenting in both external and internal arenas. *Business development and proposal writing. *Effectively use (with training) company Quality Management procedures. Your qualifications and experience The ideal candidate will have experience in the renewables industry, preferably in the windfarm sector and within the marine and coastal environment. The candidate will be responsible for the management and delivery of Environmental Impact Assessment (EIA) for renewable projects, including the coordination and leadership of multidisciplinary teams. The candidate should also be able to demonstrate a good knowledge and experience of the regulatory and legislative system, with experience in EIA and project managing medium to large projects. This position offers excellent opportunities for a dynamic and client focused individual, who can work well within a medium-sized regional team. Competitive Salary and Benefits are offered. Please apply now, or for further information please contact Sarah Green on 02074264666 or look at our website for all our roles, www.quanta-consulting.com

Tue, 19 Aug 2008 08:48:23 GMT

Tue, 19 Aug 2008 08:47:56 GMT

Operations Manager - Quality Assurance
Operations Manager - Quality Assurance ·Highly Competitive Salaries - Circa ?40k per annum upwards ·Superb Company Benefits Package ·Excellent Opportunity within the Life Sciences Sector ·Outstanding Prospects for Progression in the Company ·Excellent Industry Training and Support ·Immediate Start Available The Comp ...

Mon, 18 Aug 2008 22:00:00 GMT

Operations Manager - ?40k plus - Excellent Company
Operations Manager - Quality Assurance ·Highly Competitive Salaries - Circa ?40k per annum upwards ·Superb Company Benefits Package ·Excellent Opportunity within the Life Sciences Sector ·Outstanding Prospects for Progression in the Company ·Excellent Industry Training and Support ·Immediate Start Available The Comp ...

Mon, 18 Aug 2008 22:00:00 GMT

Biopharmaceutical Principal Scientist
Exciting opportunity to lead a team of analysts within a successful and expanding biopharmaceutical laboratory! You must have a solid background performing and validating immunoassay based technologies such as SDS-PAGE, ELISA, Western Blot, PCR and HPLC, ideally gained within a GMP environment. To learn more contact ...

Mon, 18 Aug 2008 22:00:00 GMT

Licensed Animal Technician
Our client is seeking a hands on Animal Technician as this is a small unit. The role will combine species specific animal care including breeding.38;lt59;br 47;38;gt59;38;lt59;br 47;38;gt59;The role will also involve assisting with and performing minor regulated procedures and47;or surgery, and include administration of anaesthetic.38;lt59;br 47;38;gt59;You will be working to support pre and post operative care, genotyping and collection of tissue.38;lt59;br 47;38;gt59;38;lt59;br 47;38;gt59;The ...

Mon, 18 Aug 2008 16:37:32 GMT

Analyst - Materials Science
60;strong62;Organisation Description60;47;strong62;60;br 47;62;60;br 47;62;My client is currently recruiting for a Materials Analyst based in Cambridge.60;br 47;62;60;br 47;62;60;strong62;Job Description60;47;strong62;60;br 47;62;60;br 47;62;This role involves performing routine and complex analytical experiments. You will provide high quality data for all experiments, identify anomalies in polymer properties and provide clear conclusions and next step recommendations in the context of the project ai ...

Mon, 18 Aug 2008 15:28:23 GMT

Senior Cell Culture Manager
SF025 Senior Cell Culture Manager. Cambridge. Perm. ?40k plus benefits. My client is an exciting company looking to recruit a senior cell culture manager. Key duties will involve managing the production and R & D automation teams. You will also be involved in developing and improving the cell culture processes. The ideal candidate will have a BSc/MSc or equivalent in a biological or related field and have PROVEN industrial experience in cell culture and scaling culture processes. You will also have PROVEN experience of managing large or multiple teams. Consultant: Simon Fung 01223 890811 The recruiter has stated that all applicants for this job should be able to prove that they are legally entitled to work in the UK. Carlisle Staffing plc, trading as SRG is an Employment Business/Agency. SRG winners of the 2008 Recruiter Awards for Excellence: Best Candidate Care and Best Health Care/Medical Recruitment Firm.

Mon, 18 Aug 2008 15:16:07 GMT

NMR Scientist - Biomolecular
NMR Scientist - Biomolecular Cambridge 30k My client is an exciting Biotechnology company with a great opportunity to join their drug discovery/structural sciences team. Key duties will involve applying a range of solution based NMR techniques as part of ongoing company projects. You will be responsible for studying ligand binding interactions using 1D and 2D experiments in order to determine high resolution 3D protein structures. Ideal candidates MUST have a proven background in BIMOLECULAR NMR techniques and work with Proteins/Peptides. Experience of Residual dipolar couplings and ligand binding is essential. This role would be suitable for someone seeking a postdoctoral placement to further their expertise or someone with proven industrial experience looking for a new challenge. Consultant Philippa Clark: 01223 890811 The recruiter has stated that all applicants for this job should be able to prove that they are legally entitled to work in the UK. Carlisle Staffing plc, trading as SRG is an Employment Business/Agency. SRG winners of the 2008 Recruiter Awards for Excellence: Best Candidate Care and Best Health Care/Medical Recruitment Firm.

Mon, 18 Aug 2008 15:12:00 GMT

Temporary Chemist
PULSE Scientific are pleased to be representing a world leading polymer technology organisation.38;lt59;br 47;38;gt59;38;lt59;br 47;38;gt59;Working within the Chemistry R38;amp59;amp59;D team, you will design and prepare new conjugated monomers and polymers to high standards as well as perform synthetic organic chemistry transformations.38;lt59;br 47;38;gt59;38;lt59;br 47;38;gt59;You will require a PhD or equivalent research experience in chemistry AND you will need to have a very strong kn ...

Mon, 18 Aug 2008 12:25:25 GMT

Licensed Animal Technician
Our client is seeking a hands on Animal Technician as this is a small unit. The role will combine species specific animal care including breeding. The role will also involve assisting with and performing minor regulated procedures and/or surgery, and include administration of anaesthetic. You will be worki ...

Sun, 17 Aug 2008 22:00:00 GMT

Scientist Synthetic Organic Chemistry Cambridgeshire Excellent
Scientist Synthetic Organic Chemistry Cambridgeshire 163;Excellent 60;br 47;62;60;br 47;62;Synthetic Organic Chemist. Synthetic Organic Chemist educated to PhD or with equivalent research experience in Chemistry. 60;br 47;62;60;br 47;62;The successful candidate will join our clients Chemistry R38;amp59;D Team. To join a leader in the development of high technology used in home entertainment, lighting and mobile handsets. 60;br 47;62;60;br 47;62;Responsibilities58; 60;br 47;62;60;br 47;62;183; Design and ...

Sun, 17 Aug 2008 13:58:00 GMT

DNA QC Technician
DNA QC Technician This role is on an evening shift working Sunday-Thursday 2-10pm. Salary for this role will be £16-17,000 p/a plus benefits and 13% shift allowance. PURPOSE OF THE POSITION Quality control of Oligonucleotides (MS and PAGE): ESSENTIAL JOB FUNCTIONS: Use of production database to pinpoint and communicate problems. Efficient/accurate preparation of MS equipment and reagents to perform QC tests Interpretation and analysis of mass spectra data Efficient/Accurate loading of PAGE gels in line with standard operating procedure. Interpretation of PAGE QC Data Accurate archiving of QC Data by following correct logging/archiving of data in accordance with ISO. Reagent Preparation ...

Fri, 15 Aug 2008 16:02:52 GMT

Global Safety Senior Manager
Global Safety Senior Manager ?50k - ?55k Car Allowance Job Summary: My client is a pioneering Biotechnology organisation and has been recognised as a market leading force for more than 25 years. This is an opportunity for a UK-based Sr. Manager position in the Safety Surveillance (SS) group. This function provides proactive safety surveillance across the lifecycle of products. Role/Purpose: - To provide proactive safety surveillance across the lifecycle of products. - To support the Qualified Person in Pharmacovigilance (QPPV) in the assessment, communication and actions pertaining to product safety. - To support the Global Regulatory Affairs and Safety (GRAAS) International organization in regulatory, commercial and customer interactions on safety issues. - To support the production and submission of periodic safety reports by liaising with the US-based SS staff and regional/local safety offices globally. Key responsibilities include: - Coordinate and contribute to the preparation of EU Annual Safety Reports (ASRs), Periodic Safety Update Reports (PSURs), and Quarterly Safety Update Reports (QSURs). - Oversee and support periodic safety report submissions in the EU and other regions in accordance with regulatory requirements. - Support communication of safety issues and inquiries from the regional/local regulatory authorities to the Global Safety Teams (GSTs). - Provide assistance in planning and performing analyses in support of responses to regulatory inquiries regarding safety issues. - Manage communication of safety issues and impact on data collection or retrieval between functional groups in Safety and EU Country office staff. - Respond to queries from local country officers on safety issues. - Interpret regulatory requirements and guidelines and assess impact on processes. - Support writing and review of safety-related publications. - Perform quality control activities for deliverables produced by other SS staff for the GSTs. -Guide and mentor junior SS staff members. -Lead efforts to improve processes and increase work efficiency applicable to the SS contributions to the GSTs. -Remain in compliance with active standard processes and procedures. -Contribute to training of staff regarding safety surveillance and pharmacovigilance. Basic Qualifications: - Bachelors (science preferred) or UK equivalent plus significant industry experience. Preferred Qualifications: - Masters plus significant industry experience. - Doctoral degree and several years of industry experience. - Clinical/medical research experience. - Drug safety experience in a biotech/pharmaceutical setting. - Previous management and/or mentoring experience.

Fri, 15 Aug 2008 15:52:32 GMT

Senior Scientist
SENIOR SCIENTIST - INK & DEVICE DEVELOPMENT - CAMBRIDGESHIRE Our client has a great opportunity for a Senior Scientist to work on Ink & Device Development. In this challenging role you will investigate device processing parameters to discover new processes for display fabrication in order to maximise display panel performance Ideally you will be educated to degree level or higher in organic chemistry Significant industrial exp in an ink formulation role, preferably ink jet, essential Must also be skilled in the ART of ink formulation for PLED, industrial, graphics or electronics ink jet printing applications Proficient using research grade test equipment ...

Fri, 15 Aug 2008 15:40:47 GMT

DNA QC Technician (Evenings 2-10pm)
This permanent role, based in Cambridgeshire, is for a DNA QC Technician. This role is on an evening shift working Sunday-Thursday 2-10pm. Salary for this role will be ?16-17,000 p/a plus benefits and 13% shift allowance. PURPOSE OF THE POSITION Quality control of Oligonucleotides (MS ...

Thu, 14 Aug 2008 22:00:00 GMT

Biomedical Sensor Scientist - Cambridge - Circa 30K
Biomedical Sensor Scientist - Cambridge - Circa 30K Key Skills - Biomedical Sensor Technologies - Transduction Methods - Data Analysis Based in Cambridge, a fantastic opportunity has arisen for an experienced Scientist to work with a leading technology development company. If you are degr ...

Thu, 14 Aug 2008 22:00:00 GMT

Lab Technician
We are currently recruiting for a Lab Technician. You need to have a minimum of an A-Level or equivalent in a Science subject or have worked in a scientific environment. This position is temporary. Some of the roles are working 2pm - 10pm Monday to Friday and some are normal day time hours so please specify which you would be interested in.13;10;60;33;-- Sector58; Huntingdon Lab Technician Interaction Recruitment --62; ...

Thu, 14 Aug 2008 13:42:38 GMT

Trainee Study Manager/Study Manager-Large Animal and Avian Studies - Huntingdon
Trainee Study Manager/Study Manager-Large Animal and Avian Studies - Huntingdon Huntingdon Life Sciences is one of the world's largest and most successful contract research organisations. Our company has experienced impressive growth over recent years, by creating a work environment that encourages talented individuals to thrive and make a difference. If that describes you, we offer exciting growth and career development opportunities to help you achieve your potential. Division of Environmental Sciences The Departments within the Division of Environmental Sciences provide services to the agrochemical, industrial and animal health industries, but also work with food additives and human pharmaceuticals. The Department of Large Animal and Avian Studies conducts a wide range of study types in domestic livestock species (and marker species for ecotoxicity evaluation in terrestrial vertebrates), including preclinical safety and toxicity in target and non-target animal species, pharmacokinetics, metabolism and residue studies, as required by regulatory authorities worldwide. Working within a dedicated team, you will be trained in both the practical aspects of conducting and managing these studies in accordance with the principles of GLP and in the preparation of study reports for regulatory submissions. Ideally you will have a BSc or equivalent in Toxicology, Biology or a related subject, and a keen interest in the development of human and/or veterinary medicines or in agriculture will be an advantage. Previous relevant experience, as a Study Director/Study Manager and/or in the fields of human/animal health or agrochemical development will also be advantageous, but training will be provided. Combined with your scientific knowledge, this position require someone who is organised, able to work under pressure and able to work both independently and as part of a team. In addition, there is a strong focus on providing high quality/service to our customers. If you want to make a difference and can offer what we are looking for then we want to hear from you?. Please send your CV and covering letter to careers@ukorg.huntingdon.com , or you can post it to: The Human Resources Department, Huntingdon Life Sciences, Woolley Road, Alconbury, Huntingdon, Cambridgeshire, PE28 4HS. Alternatively you can call for an application form on 01480 892500 Closing date for applications is 5th September 2008

Thu, 14 Aug 2008 08:52:49 GMT

Scientific Trainee / Assistant Study Scientist-Aquatic Ecotoxicology and Biodegradation - Huntingdon
Scientific Trainee / Assistant Study Scientist-Aquatic Ecotoxicology and Biodegradation - Huntingdon Huntingdon Life Sciences is one of the world's largest and most successful contract research organisations. Our company has experienced impressive growth over recent years, by creating a work environment that encourages talented individuals to thrive and make a difference. If that describes you, we offer exciting growth and career development opportunities to help you achieve your potential. Division of Environmental Sciences The Departments within the Division of Environmental Sciences provide services to the agrochemical, industrial and animal health industries, but also work with food additives and human pharmaceuticals. The Aquatic Ecotoxicology and Biodegradation Department conducts studies designed to help evaluate the potential risks of new and existing substances to the environment using studies conducted with aquatic plants, fish and invertebrates that are required by regulatory authorities worldwide. Working within a dedicated team, you will be trained in both the practical aspects of conducting short and long-term aquatic studies in accordance with the principles of GLP and in the preparation of study reports for regulatory submissions. Ideally you will need to have a BSc in Biology or a related subject, and must be practical, dextrous and meticulous. Combined with your scientific knowledge, this position require someone who is organised, able to work under pressure and able to work both independently and as part of a team. In addition, there is a strong focus on providing high quality/service to our customers. If you want to make a difference and can offer what we are looking for then we want to hear from you?. Please send your CV and covering letter to careers@ukorg.huntingdon.com , or you can post it to: The Human Resources Department, Huntingdon Life Sciences, Woolley Road, Alconbury, Huntingdon, Cambridgeshire, PE28 4HS. Alternatively you can call for an application form on 01480 892500 Closing date for applications is 5th September 2008

Thu, 14 Aug 2008 08:52:47 GMT

Scientist/Study Manager-Product Chemistry - Huntingdon
Scientist/Study Manager-Product Chemistry - Huntingdon Huntingdon Life Sciences is one of the world's largest and most successful contract research organisations. Our company has experienced impressive growth over recent years, by creating a work environment that encourages talented individuals to thrive and make a difference. If that describes you, we offer exciting growth and career development opportunities to help you achieve your potential. Division of Environmental Sciences The Departments within the Division of Environmental Sciences provide services to the agrochemical, industrial and animal health industries, but also work with food additives and human pharmaceuticals. The Product Chemistry Department conducts studies designed to characterise and determine the physico-chemical properties of compounds as well as assess the performance of agrochemical formulations. The role will primarily involve acting as Study Director for GLP studies, and will include performance of relevant testing, method development/validation for chromatographic analysis and timely production of study reports. We are looking for a candidate who has experience of physico-chemical properties testing or analytical chemistry within an industrial or CRO background. Applications from new or recent chemistry/analytical chemistry graduates are welcome for consideration of a role within Product Chemistry. Combined with your scientific knowledge, this position require someone who is organised, able to work under pressure and able to work both independently and as part of a team. In addition, there is a strong focus on providing high quality/service to our customers. If you want to make a difference and can offer what we are looking for then we want to hear from you?. Please send your CV and covering letter to careers@ukorg.huntingdon.com , or you can post it to: The Human Resources Department, Huntingdon Life Sciences, Woolley Road, Alconbury, Huntingdon, Cambridgeshire, PE28 4HS. Alternatively you can call for an application form on 01480 892500 Closing date for applications is 5th September 2008

Thu, 14 Aug 2008 08:52:46 GMT

Scientific Trainees-Environmental Metabolism - Huntingdon
Scientific Trainees-Environmental Metabolism - Huntingdon Huntingdon Life Sciences is one of the world's largest and most successful contract research organisations. Our company has experienced impressive growth over recent years, by creating a work environment that encourages talented individuals to thrive and make a difference. If that describes you, we offer exciting growth and career development opportunities to help you achieve your potential. Division of Environmental Sciences The Departments within the Division of Environmental Sciences provide services to the agrochemical, industrial and animal health industries, but also work with food additives and human pharmaceuticals. The Environmental Metabolism Department conducts studies designed to evaluate the metabolism and environmental fate of test substances as required by regulatory authorities worldwide. In this role you will be trained in the practical aspects of conducting metabolism and environmental fate studies. Reporting to a Study Manager, the emphasis will be on practical and analytical skills. You will learn how to assist with all aspects of the day to day running of studies to GLP standards. If you have a BSc in Chemistry or related subject, and a keen interest in laboratory work and practical problem solving, then you could be just the person we are looking for. Combined with your scientific knowledge, this position require someone who is organised, able to work under pressure and able to work both independently and as part of a team. In addition, there is a strong focus on providing high quality/service to our customers. If you want to make a difference and can offer what we are looking for then we want to hear from you?. Please send your CV and covering letter to careers@ukorg.huntingdon.com , or you can post it to: The Human Resources Department, Huntingdon Life Sciences, Woolley Road, Alconbury, Huntingdon, Cambridgeshire, PE28 4HS. Alternatively you can call for an application form on 01480 892500 Closing date for applications is 5th September 2008

Thu, 14 Aug 2008 08:52:40 GMT

Registration Manager/Senior Registration Manager - Fulbourn
Registration Manager/Senior Registration Manager - Fulbourn Syngenta is a world-leading agribusiness committed to sustainable agriculture through innovative research and technology. The company is a leader in crop protection, and ranks third in the high-value commercial seeds market. Sales in 2007 were approximately $9.2 billion. Syngenta employs over 21,000 people in more than 90 countries. Syngenta is listed on the Swiss Stock Exchange (SYNN) and on the New York Stock Exchange (SYT). Further information is available at www.syngenta.com Based at Fulbourn (Cambridge) You'll be working within the Syngenta Crop Protection Regulatory team responsible for planning, achieving, maintaining and extending Approvals/Registrations of Syngenta UK & Ireland products, ensuring that they meet marketing objectives and compliance with UK and Ireland statutory requirements. Providing the Registration Dossier and Health & Safety Data Sheets will also be your responsibility, as will project managing the production of artwork, maintaining paper work and records and staying abreast of key regulatory developments. For the role of Registration Manager you will be educated to degree level, in a science subject, preferably with a significant environmental or toxicological component. At Senior Registration level you will already have experience of working in a Regulatory position. You'll need to combine exceptional organisational skills and attention to detail with excellent communication skills and the passion to learn. We're looking for someone who can really get stuck in - someone who is happy to talk to people from all backgrounds and at all levels. Someone who can interact with functions within the Company - both in the UK and Ireland and with our Head Office in Switzerland, with external stakeholders, Regulatory Authorities and advisory agencies. What's more, we'll give you all the training you need to develop your skills and experiences to achieve top class results for Syngenta. In return, you can look forward to an attractive rewards package and excellent opportunities for career development. To apply, please email a full CV to uk.recruitment@syngenta.com quoting reference FB009. Closing date for receipt of application is 8th September with interview likely on 22nd September. For further information on Syngenta Crop Protection's products and services go to www.syngenta-crop.co.uk

Thu, 14 Aug 2008 08:52:35 GMT

Territory Account Manager
Glorious opportunity to join a leading supplier of analytical and scientific instrumentation33; 60;br 47;62;60;br 47;62;You will be responsible for the sale of both hardware and software within your territory 8211; primarily into the Life Science, Healthcare and Academic sectors. The role will include direct sales visits, telephone account management as well as the identification of new sales leads. 60;br 47;62;60;br 47;62;You will have a Science degree and ideally at least ...

Thu, 14 Aug 2008 08:06:29 GMT

Thu, 14 Aug 2008 07:55:26 GMT

Territory Account Manager
Glorious opportunity to join a leading supplier of analytical and scientific instrumentation33; 60;br 47;62;60;br 47;62;You will be responsible for the sale of both hardware and software within your territory 8211; primarily into the Life Science, Healthcare and Academic sectors. The role will include direct sales visits, telephone account management as well as the identification of new sales leads. You will have a Science degree and ideally at least 2 years hand ...

Thu, 14 Aug 2008 07:47:00 GMT

Chip Technology Technician
60;strong62;Organisation Description60;47;strong62;60;br 47;62;60;br 47;62;Our client is a large product development company for healthcare market. They produce monitoring products for the measuring of drug therapeutics providing healthcare professionals with the important information they require to manage the drug therapy of their patients. A fresh opportunity has arisen for a Chip Technology Technician60;br 47;62;60;br 47;62;60;strong62;Job Description60;47;strong62;60;br 47;62;60;br 47;62;Your ro ...

Thu, 14 Aug 2008 07:34:46 GMT

Contracts Specialist
Contracts Specialist, Cambridge CRO, 25,000 Large Clinical Research Organisation requires Contracts Specialist to join team The company is a leading global contract research ...

Wed, 13 Aug 2008 22:00:00 GMT

Lab technician
We are currently looking for Lab Technicians to work within a laboratory environment. You will need to have an A-Level or equivalent in some scientific subject or have worked in a scientific environment previously. We have two positions available, one being 9am - 5pm and one being 2pm - 10pm, please specify which would suit you. ...

Wed, 13 Aug 2008 22:00:00 GMT

Water Laboratory Technician
Our client are an environmental company in the Cambridgeshire area. They are looking for a Laboratory Technician to work on an ongoing temporary basis. The position will involve the analysis and registration of water and waste water samples, acceptance of analytical batches, stock control and maintaining qual ...

Wed, 13 Aug 2008 22:00:00 GMT

Junior Editor - Medical Communications Agency - Cambridge
Junior Editor - Medical Communications Agency - Cambridge An award winning Medical Communications agency based in Cambridge has the opportunity for an extremely talented Junior Editor to work across exciting new business wins. Reporting to the Editorial Manager and as part of a team of editors, you will be working across several projects including depression, pain and cardiovascular. In this newly created role, you will be responsible for proofreading and editing text, generating slide presentations, checking reference citations and organising artwork in addition to the typesetting of editorial projects in liaison with the account handling team. This role will also involve an element of writing and you will involve in symposia and meetings. The successful candidate will ideally have a life science degree and will have excellent communication and organisational skills. You will possess an exceptional eye for detail and have the ability to portray scientific data clearly and accurately. The ability to work well within a team as well as an individual is paramount to this role. In return you will have the opportunity to work for a market leader in Medical Communications with excellent opportunity for career progression and the chance to be part of a successful creative team within an integrated agency environment. For information on this position please contact Louise Breen on 0121 616 5143 Medical communications or medical education or medical publishing or scientific publishing or online editing or online editor or journals or editor or senior editor or editor or medical editor or junior editor or senior medical editor 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.

Wed, 13 Aug 2008 15:38:27 GMT

Senior Computer Programmer - Ref: 80191
The Wellcome Trust Sanger Institute is a world leader in genomic research, with an expanding scientific programme dedicated to understanding gene function in health & disease. The Anacode team creates the software and databases used for manual annotation of vertebrate genomic DNA sequence by a large team of annotators, who work both on and off site. Our software, written in object-oriented Perl, builds on the core Ensembl system to add the interactive tools and data sources required by our annotators to curate reference gene and transcript datasets. Our principal species are human, mouse and zebrafish. You will participate in the continued development of this system, including work on our data APIs, user interfaces, database curation Essential Skills You must have good working knowledge of a programming language such as Perl, Python, Java or C, along with UNIX experience and familiarity with relational databases. Ideal Skills Knowledge of bioinformatics and molecular biology. Experience of object-oriented Perl, user interface software development and genome scale data analysis and management. A degree in a scientific subject, and a PhD or equivalent experience. Other information You will be working in team of three other developers, sharing our software development and data curation tasks. Our team is part of the Sanger informatics group, which provides us with the backing of a large number of experienced people and extensive compute resources. Benefits Salary Range ?27,316 to ?36,951pa dependent upon experience. We offer a comprehensive range of benefits including a final salary pension scheme and excellent on-site facilities. Further details can be found on our website https://jobs.sanger.ac.uk, To submit your CV and apply for this job please go to https://jobs.sanger.ac.uk, to register and apply on line. Closing date: 5 September 2008

Wed, 13 Aug 2008 13:45:55 GMT

Research Assistant - Cambridge - ?16,892 to ?21,115
The Wellcome Trust Sanger Institute is a world leader in genomic research, with an expanding scientific programme dedicated to understanding gene function in health & disease. We are seeking to appoint a Research Assistant to support the analysis of bloods by an extensive sequence/phenotype driven mutagenesis programme. The day to day activities of the role include carrying out peripheral blood lymphocyte profiling using FACS analysis, Clinical Chemistry, Haematology and ELISA based assays. Essential Skills The successful candidate will have good communication skills, attention to detail and the ability to maintain multiple collaborative relationships successfully. Ideal Skills Experience working at containment level 2 or above would be an advantage. Experience of haematology, FACS and ELISA is desired. Other information The Mouse Genetics Programme team is carrying out an extensive sequence/phenotype driven mutagenesis programme using the resources generated as part of international efforts aimed at mutating over 95 percent of known mouse genes in embryonic stem cells by 2011. The mice and data generated by the programme will be made freely available to the scientific community as they are generated. All mutant mouse lines generated at the Wellcome Trust Sanger Institute will be examined using a common battery of phenotyping tools (see http://www.sanger.ac.uk/Teams/Team109/). Examples of the data being genera

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