Iso 13485 Jobs

As a Validation Engineer at QIAGEN Barcelona, you will lead validation activities for injection molding tools and processes to ensure compliance with ISO 13485 and GMP standards.

The QA Product Release Section Manager will manage product release activities for both manufactured and distributed products, ensuring compliance with Technical Direction guidelines and applicable…

The role involves supervising and ensuring compliance with quality standards in production processes, performing quality controls on finished products and raw materials, managing technical…

Werfen, a medical diagnostics company, is seeking a Senior Software Test Engineer to autonomously participate in verification and validation activities for clinical solutions software, including…

This role supports EMEA-wide Quality Assurance and Regulatory Affairs operations, including documenting policies, performing quality visits and audits, managing CAPA follow-up, and maintaining the…

The Lead Internal Auditor is responsible for planning and executing risk-based internal audits within regulated medical device and pharmaceutical environments, ensuring compliance with global…

SENER seeks a Senior Quality & Regulatory Compliance Manager for its Cerdanyola del Vallès center to lead regulatory affairs for medical and in-vitro devices, acting as Technical Responsible (TR) and…

The QARA Specialist will maintain and ensure the company's quality system complies with FDA, EU, ISO 13485, IEC 62304, and international medical device and IVD requirements.

Veeva Systems is seeking an experienced consultant to lead MedTech Complaints implementations for its MedTech customers globally.

INBRAIN Neuroelectronics is seeking a Senior Quality Engineer (Production) to provide technical quality leadership across manufacturing, microfabrication, and final quality control activities for…

Deneb Medical, a Donostia-based company developing robotic surgical devices, seeks a Purchasing Manager to lead its procurement strategy.