Job Description People. Passion. Possibilities. Three words that make a world of difference. More than a job. It's a chance to make a real difference. Welcome to AbbVie! As part of an international company with 48,000 employees worldwide and around 3,000 employees in Germany, you will have the opportunity of addressing some of tomorrows unmet medical needs in close collaboration with your colleagues. Are you passionate about improving global health care? Do you want to contribute to improving patients' quality of life through your expertise? In a challenging work environment that offers opportunities of developing and increasing your own skills? Youve come to the right place! Together, we break through – as Senior Auditor - RDQA Clinical Quality Audit (all genders) (full-time) In this role, you are primarily responsible for the execution of the Clinical audit program, including scheduling, planning, reporting and resolution of Clinical audits. You ensure also alignment with RDQA policies and procedures wherever possible and take the lead in the development and implementation of the Clinical Audit quality system. Recognized as Subject Matter Expert, you will provide support on GCP and quality topics and advice business partners to ensure compliance with worldwide requirements and expectations. Could be based in the following European locations – UK/ Germany/ Italy/ France/ Spain Make your mark : Assure quality and compliance in a regulated environment that includes worldwide regulations, country specific and other applicable standards and AbbVie policies as well as procedures by continuous evaluation of Clinical processes through audit and QA oversight activities. Take a lead in the Clinical audit program by planning and executing all types of clinical audits and working with auditees to resolve any non-compliance identified. Regularly taking the lead in more complex/challenging audits. Manae risk-based assessments to identify potential audits. Advance the AbbVie Quality System through leading and/or contributing to the development and implementation of systems and processes required to support global quality assurance requirements. Contribute to continuous improvement initiatives to help assure compliance regulations and corporate policies. May act as Audit Lead/SME for an assigned audit type (responsible for maintaining standards including tools/templates and guidance documents and participate in onboarding new auditors for that audit type). Mentor Clinical Audit staff and participate in and support GCP inspections, as required. Provide support and consultation to RDQA and business partners with regards to Clinical Quality and GCP regulations (Recognized as a SME).