Compliance Specialist

Position Overview : In your role as Compliance Specialist in the EMEA region you support the development and implementation of our formal corporate compliance program for a globally focused Medical Device corporation. You assist the compliance department in EMEA in implementing internal controls, performing continuous monitoring, testing and maintaining databases according to the monitoring activities. You have a high degree of independence, you are data driven and not worried by a high volume of activities and would like to work in a well-known, global Medical Device company? Then move to the next section! We are looking for a positive, passionate & open-minded collaborator to join our EMEA Legal & Compliance team in Rueil-Malmaison, France. At our company, we value attitude as much as expertise—our culture is defined by passion, creativity, and adaptability. We are looking for someone who embodies these values. Key Responsibilities: Assist in monitoring and testing programs on HCP engagement process, external funding, third-party management programs, and other processes identified as high-risk business interactions Perform testing and monitoring (T&M) activities in accordance with internal program and timelines, interacting with Finance Support the Compliance team in project management and optimization of internal Compliance processes Prepare reports and analytics relevant to T&M activities and prepare follow-up communications and corrective actions Support Transparency Reporting program for the company Develop guidance and checklist to support associate compliance with company’s requirements and boost a working environment where decisions are driven by integrity Help develop and expand the Compliance program Actively interact with various corporate functions, and instruct and update associates on compliance risk areas, policies, and procedures Coordinate with other compliance professional teams across the organization to align monitoring and testing and leverage expertise and lessons learned Required Qualifications: Compliance certificate or relevant audit experience 3-5 years of relevant experience in Compliance or internal audit Working knowledge of or familiarity with project management Demonstrated abilities in the use of technologies, IT tools, data analytics system Experience in medical devices, pharmaceuticals, or healthcare business preferred Proficiency in MS Office, particularly Excel Excellent interpersonal and communication skills Strong organizational skills and ability to work independently Ability to effectively prioritize and manage shifting priorities Ability to review and synthesize data into meaningful reports Abilit to quickly assimilate a complex regulatory environment Strong English language skills, both written and spoken If you're detail-oriented, proactive, and experienced in Compliance and/or Audit we'd love to hear from you! This is an exciting opportunity to contribute to our Compliance efforts across the EMEA region. Apply now and help drive our commitment to Compliance excellence! TerumoNeuro ComplianceEMEA ConformitéSanté DispositifsMédicaux EMEACareers MedicalDevicesJobs

Location: Rueil-Malmaison, FR

Posted Date: 7/5/2025