Become Part of the TeamWith over 35 years of experience, Flexicare is a leading designer and global provider of medical devices that enhance patient care. Headquartered in the UK, we support clinicians worldwide with class-leading devices and a global network of subsidiaries across over 100 countries. Flexicare has ambitious plans for international growth and we want you to be a part of our journey!What You'll DoBased in our office in India, you will form part of our growing global Regulatory Team, taking ownership of product registration and associated activities within key registration jurisdictions.Contribute to the creation of labels for NPNI including UDI GS1 allocation.Support the control of Revisions to Declaration of ConformityContribute on the update and maintain of external regulatory portals (MHRA, FURLS, EUDAMED)Contribute on the update an maintenance of internal regulatory databasesContribute to Non-priority EU MDR TFs completion project; contribute with DDE/risk management/GSPR/Label/IFU/TF summaryLead on the resolution of regulatory compliance matters of devices cleared in the field (CFS, tender applications).Contribute to gap analysis of standardsLiaise with all departments to support Regulatory department activitiesWho You AreWe believe you're the right fit if you haveDegree (or equivalent) in a scientific or engineering fieldMinimum 1 years' experience as a Regulatory Affairs professional in Medical Devices.Particular knowledge of regulatory requirements for medical devices including Medical Device Regulation (MDR) 2017/745 & UK MDR 2002 Part II and. ISO 13485 and ISO 14971.Strong collaborative skills- a confident and clear communicator with the ability to inform and influence diverse stakeholder groupsProficient in various software packages including but not limited to Microsoft Word, Excel, Power Point and Adobe.What You Will GetCompetitive Salary in accordance with experience and capabilitiesApplications close on Friday 13th March 2026