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1 Quality Assurance Specialist: Design Quality & Compliance Runcorn, United Kingdom Experience with Medical Device instrumentation/IVD or other heavily regulated industry * Knowledge of ISO13485:2016 (Section 7.3)/ FDA QSR Part 820.30 (Design Control), Usability for Medical Devices ...... Apply Now>>

2 Regulatory Affairs Specialist Basingstoke, United Kingdom Two years' experience within the IVD or medical device industry in regulatory affairs. * Excellent IT skills Preferred Skills/Experience: * Knowledge of IVD Directive * Excellent attention to detail... Apply Now>>