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About Us
We are a leading manufacturer of medical devices, committed to innovation, patient safety, and product efficacy. Our team is dedicated to delivering high-quality solutions that meet the needs of healthcare professionals and patients worldwide.
Main Responsibilities:
- Quality and Regulatory Affairs: Ensure compliance with industry standards and regulations, managing QA/QC and RA processes.
- Cross-functional Collaboration: Work closely with the Technical Service Manager Iberia to develop annual training plans, implement CAPA initiatives, and maintain health and safety documentation.
- Regulatory Compliance: Register products, handle health and safety compliance, and ensure timely submissions to authorities.
Requirements
- Degree in a relevant field with certifications in quality standards.
- Experience in quality management, assurance, control, and regulatory affairs.
- Knowledge of Medical Devices and quality systems.
- Proficiency in ERP systems and MS Office.
- Fluency in Spanish, Catalan, and English.
