Technical Quality Assurance Technician – France

Why Join Us?

At Excelya, we combine passion for science with enthusiasm for teamwork to redefine excellence in healthcare.

Here’s what makes us unique—

We are a young, ambitious health company representing 900 Excelyates, driven to become Europe’s leading mid-size CRO with the best employee experience. Our one-stop provider service model—offering full-service, functional service provider, and consulting—enables you to evolve through diverse projects. Working alongside preeminent experts, you will help improve scientific, operational, and human knowledge to enhance the patient’s journey.

Excelling with care means benefiting from an environment that values your natural talents, pushes boundaries with audacity, and nurtures your potential, allowing you to contribute fully to our shared mission.

About the Job

Join Excelya, where Audacity, Care, and Energy define who we are and how we work. We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand.

You will play a critical part in driving innovation and making an impact in the clinical research space, while enjoying a stimulating professional environment that encourages personal and intellectual growth.

Main Responsibilities

• Act as the Quality Assurance contact for support services across two production buildings (process maintenance, infrastructure & utilities, workplace environment, metrology).
• Contribute to the implementation and maintenance of the Quality Management System in compliance with regulations and Laboratory guidelines.
• Promote and develop adherence to Good Manufacturing Practices (GMP).
• Participate in new projects related to consolidating the pharmaceutical establishment and improving processes, equipment, and organization.
• Participate in GMP upgrades, assessing current state, proposing corrective actions, explaining them, and ensuring implementation.
• Monitor and track Quality indicators, ensuring timely follow-up and compliance with required deadlines.
• Provide internal and external responses to quality-related inquiries.
• Update and verify site documentation, including procedures, SOPs, and contracts.
• Manage quality risks (identification, analysis, control) and contribute to deviation processes.
• Draft and manage deviations, including impact assessment, investigations, action plans, and closure.
• Follow up on corrective/preventive actions to ensure effectiveness.
• Contribute to internal audits and ensure compliance with standards.