Save Job Back to Search Job Description Summary Similar JobsA 4 day working week, allowing for more flexibility and better work life balanceCutting edge business with real world impactAbout Our ClientOur client is a cutting edge medical device manufacturer. They have multiple marketed products, as well as new products awaiting registration in UK, EU and ROW markets.Job DescriptionCoordinate and manage regulatory submissions and approvals in line with industry standards.Ensure compliance with applicable regulations and guidelines within the life sciences industry.Monitor regulatory changes and update internal processes as required.Provide strategic advice on regulatory matters to support business objectives.Develop and maintain relationships with regulatory authorities and key stakeholders.Prepare and review documentation to ensure accuracy and compliance.Collaborate with internal teams to align regulatory strategies with organisational goals.Support audits and inspections related to regulatory compliance.The Successful ApplicantProven record of working with Medical device regulations, and liaising with regulatory bodies.Good knowledge of QMS activities.What's on OfferCompetitive salary4 Day Working weekPermanent position based in West LondonContactJames HarrisQuote job refJN-012026-6918499Phone number+441142636001Job summaryJob functionLife SciencesSubsectorRegulatory AffairsSectorHealthcare / PharmaceuticalLocationWest LondonContract typePermanentConsultant nameJames HarrisConsultant phone+441142636001Job referenceJN-012026-6918499
