Save Job Back to Search Job Description Summary Similar JobsOpportunity to lead the regulatory affairs function for India, M.E. & AfricaOpportunity to work with senior leadership from multiple geographiesAbout Our ClientThe client is one of the leading global medical devices player and has operations in multiple countries around the globe. They operate extensively in the Radiation, Oncology and Neurosurgery domain, among other therapy areas.Job DescriptionManage all aspects of regulatory submissions and correspondence with regulatory agencies.Develop and implement strategies for earliest possible product approval and maximum product life cycle.Monitor changes in regulatory legislation and guidelines, advising on impact for the business.Ensure company procedures are in compliance with regulatory requirements and standards.Represent the Regulatory Affairs function in project teams and management teams.Be the point of contact for all regulatory matters in the geographies of India, Turkey, Middle East and AfricaThe Successful ApplicantThe successful candidate should have -15+ years of overall experience in the regulatory affairs domain in the medical devices industry.S/he should have had an exposure of presenting to regulatory bodies - the technical know-how should be coupled with an authoritative presence in order to work closely with senior internal and external stakeholders.This will be an individual contributor role, but the candidate should have an experience of working with global senior stakeholders.Candidate should have an extensive experience of working in the medical devices technology industryWhat's on OfferOpportunity to lead and influence regulatory affairs within a prominent player in the medical devices sector.Quote job refJN-082024-6519467Job summaryFunctionHealthcare & Life SciencesSub SectorRegulatory AffairsWhat is your area of specialisation?Medical Device / Medical EquipmentLocationGurgaonJob TypePermanentJob ReferenceJN-082024-6519467
