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Qualified Person - Contract Manufacturing Organisation - Northern UK Nr ref.: /JOBS.pl The Qualified Person will be; Performing quality audits and technical reviews during visits to both customers and suppliers Responsible for batch record review and release, also any other such duties required from within the team Responsible for on site management of the QMS including technical agreements, deviations, customer complaints, change controls and CAPA's Responsible for liaison with external laboratories used on the companies CHC licenced product, maintaining a working knowledge of their quality standards and capacities to ensure efficient and robust service to the company The ideal candidate for this position will be qualified to degree level or equivalent and possess a minimum of 1 year's previous experience as a QP on a UK licence. This position will be based on site in the Midlands and offers a comprehensive salary and benefits package as well as the chance to progress and develop within the company. Please contact me for further details. Click here to apply for this job this position At RBW Consulting LLP, every one of our consultants has the benefit of five years experience in helping Pharmaceutical Professionals find the jobs they are looking for in the industry. With unrivalled industry knowledge and excellent links with hiring managers in Biotechs, Pharmas and CROs throughout the UK, Europe and across the world, we would be delighted to speak with you about the role you are looking for. Call (0) or email for a confidential discussion about your options for progression. Keywords: CPM, Clinical, Antwerp, Brussels, Liege, Belgium, Holland, Netherlands, Programme, Program, Study, Studies, Trials, Matrix, International, CRO, Pharma, Pharmaceutical, Clinical Research Organisation, Organization, Targets, Target, Operations, Operational, Costing, Clinical Project Manager, Project Manager, Global Clinical Project Manager, Global Project Manager, PM, Operations Manager, Study Operations Manager, Study Manager, Clinical Study Manager, Global Study Manager, Global Study Operations Manager, Holland, Netherlands, CRA, Senior CRA, Lead CRA, Clinical Research Associate Kontakt: Aplikuj teraz Ogłoszenie pochodzi z serwisu Jobs.pl .

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