You will be joining an ISO9001:2008 accredited contract research organisation (CRO) providing the pharmaceutical industry with chemical development services.
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Working in a team of four, you will be responsible for the maintenance and repair of cGMP-certified control systems for process plant and equipment, solvent recovery systems and utilities including boilers, compressors and refrigeration.
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As a member of the Operations team, and reporting to the Study Manager, the Analyst will be responsible for performing lab work as directed by their line manager.
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As a member of the Operations team, and reporting to the BioAnalytical Department Head, the Study Manager will lead a small group of Analysts. The Study Manager will be expected to provide technical expertise for development of custom assays and technical transfer of client assays, as well as project management of testing client samples.
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As a member of the Operations team, and reporting to the Department Head, the Study Manager will lead a small group of Analysts providing technical expertise and co-ordinating the routine testing of client samples.
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You will develop pharmaceutical formulation strategies to improve solubility, oral bioavailability and efficacy of poorly-soluble drugs.
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As a member of the Operations team, and reporting to the Department Head, The Microbiology Study Manager will lead a small group of Analysts.
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The current position offers the successful candidate the opportunity to develop within a rapidly expanding company.
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The Development Scientist will work within a team on contract and internal development projects. These include developing immunoassays such as lateral flow tests and emerging rapid diagnostic technologies.
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The Quality Auditor will work closely with the other members of the Quality team and the Operations team and will be involved in ensuring implemented systems, processes, equipment and materials are GMP and GLP compliant.
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The Quality Specialist will work closely with the other members of the Quality team and the Operations team and will be involved in ensuring implemented systems, processes, equipment and materials are GMP and GLP compliant.
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The V&V Engineer will be responsible for working within the research and development department on developing new technologies, new products and processes for blood glucose measurement, insulin delivery and diabetes disease management and their transfer into operations.
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Reporting to the R&D Director, the Industry Standards & External Environment Engineer will be responsible to work within the research and development department on developing new technologies, new products and processes for blood glucose measurement, insulin delivery and diabetes disease management and their transfer into operations. This will include translating industry standards to enable internal resources to deliver quality and compliant products.
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Reporting to the R&D Director, the Requirements Engineer will be responsible to Work within the research and development department on developing new technologies, new products and processes for blood glucose measurement, insulin delivery and diabetes disease management and their transfer into operations.
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The successful candidate will be required to work with the company's crystallisation development team on a number of scale-up projects.
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For candidates who have yet to acquire global regulatory affairs experience this opportunity represents an immediate and significant development opportunity. For candidates who have already gained global exposure this role still offers enormous potential as the division is wholly responsible for all global registrations.
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Due to expansion, this company requires a Salt/Polymorph Screening Scientist to undertake project work.
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We are looking to recruit a dynamic Territory Sales Manager. This demanding but rewarding position carries key account responsibilities within the Cardiac Anaesthesia environment.
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