* Manage technical aspects of manufacturing and quality control, including technology transfer, process optimization, investigations, and troubleshooting.
* Review and approve technical and GxP documentation to ensure compliance with cGMP, Quality Assurance, and regulatory requirements.
* Oversee Change Controls and support internal stakeholders, such as Regulatory Affairs and Quality Assurance.
* Provide expertise in pharmaceutical manufacturing, analytical methods (e.g., HPLC, sterility testing), and GxP compliance.
* Coordinate with external partners (CMOs, analytical labs, API suppliers) to ensure smooth technical exchanges.
* Support the follow-up of quality control activities, including stability studies and reference standards management.
* Master's degree in Life Sciences (Pharmacy, Chemistry, Biotechnology, etc.).
* At least 5 years of experience in a GMP-regulated pharmaceutical environment with expertise in manufacturing (oral forms, injectables) and analytics.
* Strong knowledge of quality assurance processes, including Change Controls, CAPAs, and investigations.
* Proactive, autonomous, and capable of managing multiple projects simultaneously.
* Strong communication skills and ability to work in cross-functional, international teams.
* Willingness to travel (approx. 5-10%).
* Fluency in English is required; French is highly desirable, and additional languages are a plus.
* A key role in a dynamic, fast-paced company with experienced professionals.
* The opportunity to contribute to strategic decisions and projects.
* A full-time position with competitive remuneration.
* A modern work environment that promotes work-life balance.
Would you like to take on this exciting challenge? We look forward to receiving your application.