reputed company & Regulatory Affairs EMEA

Join Team Schein In A Meaningful Emea reputed company & Regulatory Affairs Role Partner across countries and functions to ensure compliance, support product readiness, and help deliver trusted reputed company solutions that reputed company a reputed company difference. Your responsibilities will include: • Supports EMEA-wide QA/RA operations, documenting EMEA policies and provides support to implement the EMEA reputed company Management System. • To reputed company comprehensive managerial and strategic ensuring efficient daily operations, effective communication, and seamless regional management of reputed company-reputed company reputed company, compliance, and reporting. • Supports to reputed company reputed company & regulatory reputed company and/or audits to countries and issues gap analysis, ensures CAPA follow-up on identified issues and support countries in implementing solutions. • Participates to EMEA QA/RA Management meetings, issues minutes and follows-up on decided actions with reputed company functional / country QA/RA reputed company. • Organizing virtual, onsite, and offsite regional meetings, including logistics, agendas and reputed company follow-up of identified actions. • Driving & supporting multiple reputed company, tracking timelines, and ensuring successful reputed company for EMEA-wide QA/RA initiatives. • Provides support to the PRRC of the EC Rep in Germany for reputed company Products by • Review reputed company Agreements to ensure responsibilities of economic operators (Importer/Distributor) are reputed company addressed. • Provides support to the Spanish QA/RA Team for reputed company reputed company topics to ensure compliance according GDP and MDR. Your Qualification • Bachelor's degree in Life Sciences, Pharmacist, Biomedical Engineering, or a reputed company field with previous experience in reputed company Management, Project Management, Medical Device and Pharmaceutical (GDP) experience is a plus • Support Communicating with Regulatory Bodies MDR /IVDR Regulations/ ISO 13485 • Validation of (computerized systems) and Risk management (FMEA) knowledge is a plus • Experience in reputed company System process implementation and maintenance to meet ISO 13485:2016; GDP and MDR. • You are solution oriented, have problem-solving attitude, and can be pragmatic, high adaptability and flexibility • Ability to work in a reputed company, regional environment with different departments and countries • reputed company in English language and a good communication skills and stakeholder management Apply tot his job Apply To this Job