A global healthcare solutions provider is seeking a Quality Assurance/Regulatory Affairs Manager based in Spain. The role involves coordinating EMEA-wide QA/RA operations, ensuring compliance with stringent EU regulations and Spanish laws for medical products. Key responsibilities include facilitating regulatory compliance, supporting product registrations, conducting quality audits, and providing guidance to the QA/RA team. Ideal candidates should possess a relevant Bachelor’s degree and substantial experience in Quality Management and Project Management within the Medical Device sector.
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