Quality Assurance Manager & GCP Auditor

Das ist der Job

Support vendor selection, qualification, and ongoing oversight.

Darum lohnt es sich

This position combines independent quality oversight with auditing responsibilities across internal processes, sites, systems, projects, and service providers, while supporting adherence to GCP-Service SOPs and alignment with national and international regulatory requirements.

Collaboration and Professional Contribution Communicate proactively with team leads and process and CAPA owners. Strong understanding of Good Clinical Practice (GCP) and applicable national and international regulatory requirements. Monitoring experience, ideally in an international setting, is an advantage.

Preferred Location: Germany (BREMEN) or the Czech Republic (PRAGUE) The Quality Assurance Manager plays a key role in safeguarding the quality, integrity, and compliance of our clinical research activities.

If you enjoy working in a structured environment, improving systems, and contributing to high-quality clinical research, this is an excellent opportunity to make a meaningful impact.

Responsibilities Documentation and SOP Management Provide QA guidance on SOPs and controlled documents, and manage the development, review, improvement, deviations, and follow-up actions for company SOPs, forms, and related documentation.

Audits and Vendor Oversight Conduct internal and external audits, including site, system, process, project compliance, service provider, sponsor, and vendor audits. Quality Systems and Compliance Manage CAPAs, track progress, and support continuous improvement of the QMS.

Support investigations into compliance issues reported to QA, including root-cause analysis. Escalate critical compliance issues and support Critical to Quality and risk identification and mitigation. Contribute to meetings, projects, and training, and propose solutions. Support QA administration and follow company SOPs.

Stay informed on services and stakeholder needs. Keep up to date with industry standards. Travel as needed, including overnight stays. Requirements Education and Clinical Research Experience Degree in Life Sciences or an equivalent biological or medical qualification, or relevant clinical research experience.

At least 3–5 years of experience in clinical research, life sciences, or a related QA environment. Auditing and Regulatory Expertise At least 3 years of experience as a Quality Assurance Manager and GCP auditor, with the ability to act independently and objectively.

Quality Systems and Process Knowledge Solid knowledge of the clinical research process and practical experience with quality systems, CAPA management, or compliance activities.

Communication and Working Style Strong communication skills and the ability to work independently, collaboratively, and with an open-minded, structured, solution-oriented approach. Proficiency in Microsoft Office. #J-18808-Ljbffr