Senior Quality Assurance Manager

Role Overview We are seeking an experienced and motivated We are seeking an experienced and motivated Senior Quality Assurance (QA) Manager – Clinical Trials, with a focus on the GCP-regulated environment, to further develop our QA function within the clinical research environment. This role combines hands‑on quality expertise with close collaboration with cross-functional and international stakeholders. Key Responsibilities Plan, conduct, report and track internal and external audits (e.g. process audits, vendor qualification audits, system and study specific audits and inspections) Ensure compliance with GCP, ICH guidelines, FDA regulations, applicable regulatory requirements, and company standards Own and manage Deviation and CAPA processes, including root cause analysis, tracking, and effectiveness checks Drive risk management activities, including risk assessments and mitigation strategies Lead and support change management processes related to quality systems and clinical operations Responsible for the creation, review, approval, and lifecycle management of QA SOPs Preparation of role‑based training materials and conduct of training courses in the GCP/FDA regulated setting Prepare quality metrics, management reports, and audit summaries for upper management Act as a key QA contact for regulatory inspections and sponsor audits Collaborate closely with Clinical Operations, Project Management, Regulatory Affairs, Data Management, Medical Writing and external partners Support continuous improvement initiatives within the Quality Management System (QMS) Review and approve validation documentation (e.g. validation plans, risk assessments, test scripts, validation reports) for computerized systems, including eQMS and other GxP-relevant systems Qualifications & Experience University degree in Life Sciences, Pharmacy, Medicine, or a related field Several years of professional experience in Quality Assurance within clinical trials, ideally within a GCP regulated enviroment Familiarity with clinical trial processes across Phases I-III. Senior QA professional Strong knowledge of GCP, ICH and international regulatory requirements (e.g. FDA regulations) Act as the GCP Quality Assurance expert and primary point of contact for GCP compliance matters in global and multi-regional clinical trials. Demonstrated experience in: Audit planning and inspection readiness, performance, and reporting Deviation and CAPA management Risk management Change management SOP and training management Willingness to travel nationally and internationally, particularly within/to Germany, within Europe and the USA Strong organizational, analytical, and problem‑solving skills Confident communication style and ability to work with stakeholders at all levels What We Offer A responsible senior role in an international clinical research environment High level of autonomy and the opportunity to actively shape QA processes Collaboration with global teams and exposure to international projects A thorough and practice-oriented onboarding Performance-based compensation and flexible working hours A company culture strongly characterized by trust and collegiality An exciting workplace with opportunities for professional and personal development, for example development into a team lead function #J-18808-Ljbffr Tranquil Clinical Research and Consulting Services