Senior Quality Leader - ISO 13485 & Cleanroom Compliance

Celestica is seeking a Quality Manager for Medical Device QMS and controlled environments in Spain. Lead ISO 13485 alignment, update documentation, and support audits. Manage CAPAs, NCRs, and critical systems, while overseeing cleanrooms and supplier testing to ensure compliant production and release to customers. Requirements include 10 years in Microbiology/Lab Management in Medical Devices, plus strong regulatory knowledge and leadership. Fluency in English; Spanish preferred. J-18808-Ljbffr