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Job Description The Quality Compliance Specialist is responsible for coordinating and executing the regional Quality Compliance program across EMEA. This role leads the planning and performance of internal audits, supports external regulatory and certification audits, prepares Management Review reports, and contributes to the effective operation and continuous improvement of the Quality Management System (QMS) throughout the region.
Analyze quality metrics and trends to support Management Review discussions and decision‑making.
Support maintenance and continuous improvement of the Quality Management System in accordance with applicable regulations and standards.
Provide guidance to functions and sites on quality compliance requirements,



audit readiness, and best practices.
Support Quality activities across the region, including CAPA management, quality risk management, document control, change management, training compliance, and quality reporting, as required.
Collaborate with regional and integral Quality teams to ensure alignment of compliance initiatives and quality objectives.
Promote a culture of quality, compliance, and continuous improvement throughout the organization.
Bachelor's degree in Life Sciences, Engineering, Quality Management, or a related discipline.
Minimum 3–5 years of experience in Quality Assurance, Quality Compliance, or Quality Systems within a regulated industry (Medical Devices, Pharmaceutical, Biotechnology, or similar).
Experience planning and conducting internal audits. Experience preparing management review materials and quality metrics analysis.
Strong knowledge of Quality Management Systems and applicable regulations and standards (e.g., Fluent in English;

📌 Quality Specialist - Training (Comunidad Valenciana)
🏢 BD
📍 Comunidad Valenciana