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My Client, an International Medical Solutions business, is hiring a QC Analyst for their Farnham based team. The salary range is £28k£36k (pro rata) depending on experience. This is a 6-month FTC as an employee with a 5% completion bonus, and includes access to pension and healthcare etc. The role provides analytical testing support for all pharmaceutical products manufactured at the Farnham site. Following the clients Quality Standards or Pharmacopoeia methods testing will cover raw materials, excipients, components, in-process samples and finished products. Testing will include a high proportion of visual and physical measurements associated with the testing of components.Performs qualitative tests or quantitative assays on samples using techniques that vary from use of standard analytical equipment to highly modern and automated instrumentation. Responsibilities will also include documenting all work in a compliant manner, participating in OOS investigations, reviewing of analytical results to ensure accuracy and compliance to test methods, preparation of all laboratory documentation. Ensure that departmental objectives are implemented in line with the overall Quality/Corporate goals. Comply with all safety and GMP requirements within the Laboratory. Plan a daily schedule to meet testing requirements. Preparation and timely submission of test samples from raw materials, in-process and final product samples to both internal laboratories and to external test houses. Operation of laboratory equipment including daily up-keep and maintenance and assist in trouble-shooting when required. Working to Standard Operating Procedures/WIs, complete the sampling, inspection and analysis of Raw Materials or Components, In-Process and Final Product samples to defined Chemical, Physical and Pharmacopoeia test procedures to support Manufacturing and Development activities. Document all testing activities to regulatory standards. Review analytical results to ensure accuracy and compliance to both test methods and registered specifications. Preparation and revision of laboratory protocols, reports, procedures and WIs. Assist in the Innovation and development analytical processes to meet internal and international method validation requirements to support any QC, R&D or Manufacturing activity. Lead OOS/OOT investigations, utilising technical knowledge to identify assignable cause and corrective actions. Lead and participate in investigations for Quality Events, Complaints and review/generation of Change controls. Manage information to support monitoring and evaluation of cGMP compliance including Key Performance Indicators (KPI). Prepare metrics to visualise KPIs. Participate in and facilitate improvement programs within the Laboratory. Participate in multi-functional teams to support project assignments. Ensure that all interactions and engagements are carried out with the highest ethical and professional standards and that all work is accomplished with quality and in accordance with the Clients values. Complete additional tasks considered necessary to meet business and customer requirements as indicated by the team leader. Carry out other reasonable tasks as required by the Team leader. Education and Experience Be educated in science or related discipline. Possess relevant experience in the Pharmaceutical Industry. 1-2 years experience in an analytical Laboratory is preferable. A knowledge of quality systems and the experience of working in a regulated environment preferred. Have a good knowledge of GLP/GMP. Knowledge and experience in the following analytical techniques: Gas chromatography and HPLC/UPLC An understanding and application of COSHH regulations in a chemical industry. Demonstrated advanced computer skills Microsoft Office preferred. Good written and verbal skills. To perform precise and constant analysis in support of analytical testing. To complete assignments in a timely manner and communicate progress at intervals. To analytically evaluate results. Be a self-starter capable of delivering consistent results to a high level. Must be a team player and be able to interact with colleagues in a constructive and positive manner TPBN1_UKTJ