Save Job Back to Search Job Description Summary Similar JobsThe client benefits amid rising demand in a high-growth marketA newly created position in their structure, with freedom to shape the roleAbout Our ClientOur client is a Medical Device business, headquartered in the UK.Job DescriptionDevelop and Execute the regulatory strategyProvide guidance in relation to Product Safety EvaluationOversee regulatory submissions for FDA and EU MDRFinal sign off on artwork, warnings, and safety documentationWork cross functionally with R&D to foster a strong NPD pipelineAssist the teams with global expansion, considering changes in the global regulatory landscapeThe Successful ApplicantExtensive experience in Medical Device industry, focusing on Regulatory AffairsProven leaderFDA and EU MDR submissions experienceWhat's on OfferCompetitive package. This is a new role, so that client is willing to listen to the market, and pay what the market dictates25 Days leave + Bank holidaysHybrid workingEV SchemeOn site GymContactJames HarrisQuote job refJN-092025-6840032Phone number+44 172 773 0106Job summaryJob functionLife SciencesSubsectorRegulatory AffairsSectorHealthcare / PharmaceuticalLocationCheshireContract typePermanentConsultant nameJames HarrisConsultant phone+44 172 773 0106Job referenceJN-092025-6840032
