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Job Title: Validation SpecialistLocation: Speke, LiverpoolRate: Up to £35,000 dependent on experienceWorking hours: Mon - Fri (37.5hr per week)Contract: 12 months (strong potential to be permanent after)Start date: ASAP (November ideally)SRG have a fantastic opportunity to join a team of scientists within the Analytical Science and Technology department that conduct quality control method validation of the flu vaccine. The ideal candidate will have a science degree and some GMP experience, although graduates with a strong laboratory background will be considered.Key Responsibilities:* You will design experiments on key projects that involve new technologies and processes to QC* You will troubleshoot technical issue and develop existing methods to improve analytical testing technologies. * The role will involve GMP execution of development and technical assays in support of both egg and cell characterisation samples.* You will review data generated from validation activities and assess any detrimental trends or deviation identified.Requirements:* BSc in a scientific subject* Experience in SDS PAGE, UPLC, Chromatography, method validation or QC is preferred but not essential.* Solid understanding of GMP.If this role is of interest to you, (or you know anyone who might be suitable), please email your CV to Tom O'Neill at firstname.lastname@example.org and a time that is convenient for me to call you.