Regulatory and Quality Compliance Manager

hace 5 días

madrid, España elemed A tiempo completo

The company Are 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? 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. 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 Maintain the Quality Management System for their Spanish Organization Work with the Regional Commercial leader to ensure the medical device portfolio remain commercially available and compliant Leading clinical data collection and surgeon feedback processes for submission and PMCFs Prepare and lead the quality management review meetings Training and coaching people in RAQA functions in other EMEA offices on the procedures and processes Identify local regulatory requirements and lead impact assessment which is driving quality management system changes Execute Local regulatory registrations where necessary EMEA regulatory affairs activities concerning importer and authorized representative requirements At least 5 years in a quality assurance or regulatory affairs role in the medical device industry Led the RAQA operations or projects for medical devices Fluent written & spoken in Spanish and English (bonus if Portuguese and Catalan as well) Office-presence 3 days per week in Barcelona city-centre ✉️ We serve within the Medical device, diagnostic and combination device arena, working with Managers up to VP of Quality and Regulatory. Our team helps medical device experts of today become leaders of tomorrow. #At Elemed, we recruit exceptional people that solve regulatory and compliance problems, so patients can have access to safe, innovative and life-changing Medical Devices. Learn and develop as a regulatory, quality or clinical professional with 1 : 1 mentorship from a highly experienced mentor. Our mentors are some of the most inspirational and talented senior professionals in the medical device and IVD industry. Join hundreds of fellow regulatory, quality and clinical professionals in Elemed’s RQC Network. We are an equal opportunity employer and value diversity at our company #J-18808-Ljbffr

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