Quality Regulatory Manager

hace 4 días


Barcelona, España elemed A tiempo completo

RAQA Lead - Spain and PortugalAre you someone who has Iberia-wide regulatory experiences and are looking for the next step in your medical devices career at the EMEA level? Are you someone who likes to think creatively and prioritizes medical devices that are always accessible to patients and surgeons on the market? Do you like working with both active and non-active devices?Here is a rare and great opportunity to join an international leader in surgical technology and be part of this company’s regional growth strategy in Spain and Portugal and be visible at the EMEA-level. As the Regional QARA Lead for the IBERIAN region, you will be based at their Spain branch office in Barcelona, where they have centralised sales, marketing, customer success teams all in one place.This is a company‑critical role and your past experiences in registrations can help the company to reach their business goals for the EMEA region.This exciting position will give you the opportunity to work in a diverse international environment.You will be responsible for the quality system of the sales office in Barcelona as well as supporting the registrations for Spain. Furthermore, you are part of the EMEA Quality Assurance and Regulatory affairs team, for this region you will be responsible for collecting clinical data from surgeons to assist the HQ in the US with clinical surveillance.In this role you will report directly to the Sr Director Quality Assurance and Regulatory Affairs International.ResponsibilitiesMaintain the Quality Management System for their Spanish OrganizationWork with the Regional Commercial leader to ensure the medical device portfolio remains commercially available and compliantManage Post‑Market Surveillance (PMS) operations and PMCFsLead clinical data collection and surgeon feedback processes for submission and PMCFsPrepare and lead the quality management review meetingsTraining and coaching people in RAQA functions in other EMEA offices on the procedures and processesIdentify local regulatory requirements and lead impact assessment which is driving quality management system changesExecute Local regulatory registrations where necessarySupporting internal and external auditsEMEA regulatory affairs activities concerning importer and authorized representative requirementsQualificationsAt least 5 years in a quality assurance or regulatory affairs role in the medical device industryLed the RAQA operations or projects for medical devicesFluent written & spoken in Spanish and English (bonus if Portuguese and Catalan as well)✉️ If you are interested in this exciting role, please send your application directly to .Please note: Only candidates meeting the requirements set out in the role profile above, will be considered in the application process.Due to the high volume of applications we receive, our team might not be able to contact each applicant individually regarding the status of their application. If you do not hear from us after 10 days, please consider your application unsuccessful.Seniority levelMid‑Senior levelEmployment typeFull‑timeJob functionQuality Assurance, Business Development, and LegalIndustriesMedical Equipment Manufacturing and Hospitals and Health Care⚖️ We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.#J-18808-Ljbffr



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