/"Expect to grow/", personally and professionally: At Siegfried, we offer exciting challenges and ample opportunities to showcase your talents. As a trusted and respected partner to the pharmaceutical industry, we uphold the highest standards in safety, quality and sustainability, while fostering a culture that empowers you to thrive. Join a rapidly expanding global company, where diverse perspectives and experiences come together in a collaborative environment. Here, you'll find a workplace that values both collective success and your individual contributions—offering long‑term opportunities to grow and make an impact.

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Your Role:
- Ensure compliance with GMP requirements, ISO 13485 standards, ICH guidelines, the Siegfried Quality Manual, and all applicable SOPs across site operations.
- Lead and manage the Quality Assurance (QA) and Quality Control (QC) functions.
- Ensure that all site products, projects, processes, strategies,



and decisions comply with applicable GMP, ISO 13485, and Siegfried Quality requirements.
- Serve as the primary point of contact for Global Quality matters and ensure the effective implementation and ongoing adherence to Siegfried Quality policies and standards.
- Define, execute, and monitor the annual departmental budget. Ensure the effective allocation and utilization of human and financial resources to achieve departmental objectives efficiently.
- Foster a quality‑first culture and continuous improvement mindset across the site.
- Provide overall leadership and accountability for product quality, patient safety, regulatory compliance, and quality performance.
- Lead the site's Quality Strategy and Quality Plan, ensuring continuous improvement and alignment with corporate objectives
- Act as the Medical Devices Management Representative, assuming the responsibilities and authority defined in ISO 13485.
- Ensure compliance

📌 Site Quality Head (Barberá del Vallés)
🏢 SIEGFRIED BARBERA
📍 Barberá del Vallés