Senior Specialist Quality & Regulatory Affairs EMEA

Supports EMEA-wide QA/RA operations, participating to EMEA QA/RA Management meetings, documenting EMEA policies, accompanying the Snr. Director QA/RA EMEA to perform quality visits to countries and issue gap analysis, ensures CAPA follow-up on identified issues and support countries in implementing solutions within the Global Distribution Group Henry Schein Sites in EMEA. ESSENTIAL DUTIES AND RESPONSIBILITIES: Supports EMEA-wide QA/RA operations, documenting EMEA policies and provides support to implement the EMEA Quality Management System.  Supports to perform quality & regulatory visits and /or audits  to countries and issues gap analysis, ensures CAPA follow-up  and related documentation on identified issues and support countries in implementing solutions. Organizing virtual, onsite, and offsite regional meetings, including logistics, agendas  and close follow-up on decided actions with related functional / country QA/RA Lead. Support and assistance to Exec. Director QA & RA EMEA and the EMEA QA/RA Team Support to multiple projects, tracking timelines, and ensuring successful outcomes for EMEA-wide QA/RA initiatives. Maintenance of eQMS and Quality Document Management Tool  Oversight of change control activities and CAPA follow-up, timely closure Provides support to the country QA/RA Teams in Quality related topics to ensure compliance according GDP and MDR.   Implementation of regulatory requirements and continuous improvement, support to ongoing transformation projects and product launch activities Support roll-out eQMS implementation in identified countries.  o Inspection readiness initiatives and to roll- of required tools o Conduct and oversee quality training and compliance communications. Assits PRRC and EC Rep responsibilities such as adverse event reporting, post-market surveillance and FSN management Other tasks and projects as needed Physical Activities: Job holder based in  any country in EMEA  Home based – ready to travel regularly (up to 30%) QUALIFICATIONS:

Quality Management, Project Management experiences, Medical Device Experiences, Pharmaceutical (GDP) experience is a plus MDR /IVDR Regulations/ ISO 13485  Validation of (computerized systems) and Risk management (FMEA) knowledge is  a plus               Education: Bachelor’s degree in Life Sciences, Pharmacist, Biomedical Engineering, Business management or a related field.          Specialise d Knowledge and Skills: Knowledge and understanding of Quality Management Systems  and Project Management Quality System process implementation and maintenance to meet ISO 13485:2016; GDP and MDR.   Solution oriented, problem-solving attitude, pragmatic, high adaptability and flexibility  Ability to work in a matrix, regional environment with different departments and countries  English speaker Good communication skills and stakeholder management                           Other: Balances a sense of urgency of time pressures with adherence to all regulatory requirements.  Sensitive in dealing with confidential Information Demonstrates advanced oral and written communication skills  Must be fluent in written and spoken English Information on pay transparency pursuant to Directive (EU) 2023/970 Please note that we comply with the relevant legal obligations regarding pay transparency, in particular those set forth in the EU Pay Transparency Directive (Directive (EU) 2023/970) and its respective national implementation. In this context, we will inform you of the starting salary or the corresponding salary range for the advertised position no later than before the first job interview or before a personal discussion of your application. This information is based on objective, gender-neutral criteria established for the position in question. Please note that we will not ask about your current or previous salary during the rest of the process in order to ensure equal pay. This notice does not