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…
As a Senior Clinical Development Lead and Medical Safety Physician, you will oversee the full product safety lifecycle for Roche-branded products.
As a Clinical Site Manager specializing in IVDR and Study Start-Up, you will lead end-to-end study start-up activities, including site selection, activation, and regulatory submissions.
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…
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.
Roche is hiring a Clinical Selling Specialist based in Toledo, Spain, to drive adoption of biomarkers and innovative solutions in the Castilla-La Mancha region.
This role involves executing test protocols and functional validation on in-vitro diagnostic (IVD) instruments during development, troubleshooting issues, and providing technical support.
SGS is hiring a Global Team Leader for IVDR to lead the team of IVDR product assessors and IHC, provide technical expertise on in vitro diagnostic medical device certification, and ensure compliance…
An R&D Specialist is needed to evaluate and test an in vitro diagnostic instrument in development, participating in nucleic acid assays using PCR and developing test workflows.
SpotLab, an AI laboratory in Madrid, seeks a Business Development Lead to drive AI oncology solutions to market, focusing on the MEDULAI product for blood cancer diagnosis.
SpotLab, a Madrid-based HealthTech startup, is seeking a Regulatory & Quality Lead to certify AI-based IVD diagnostic products, particularly for microscopy images in hematology and infectious…