CMC Project QA manager

About the Job At Excelya, we embody Audacity, Care, and Energy. We are seeking a dedicated CMC Project Quality Insurance professional to join our team, where you will be instrumental in ensuring quality throughout the CMC (Chemistry, Manufacturing, and Controls) processes. This role provides an exceptional opportunity to work in a supportive environment that prioritizes collaboration and innovation. In this position, you will work closely with cross‑functional teams to uphold the highest quality standards for our CMC projects, facilitating compliance with regulatory requirements and contributing to the overall success of product development. Main Responsibilities Quality monitoring of product development projects (in‑house or outsourced) for CMC (Chemical Manufacturing and Control) As a member of the CMC project team in the role of QA‑CMC, you will ensure the overall quality of pharmaceutical development activities from the active ingredient to the investigational medicinal product (end to end) Participating in the drafting and updating of quality agreements Evaluating and ensuring the compliance of deliverables and development support studies necessary for the preparation of drug specification files (PSF) with current quality standards (quality review of Product Specification Files, techniques, standards, protocols/stability reports/validation and analytical transfer, expiry dates, MBR, etc.) and deliverables supporting the drafting of marketing authorisation files Reviewing files for clinical batches of active ingredients and investigational injectable medicinal products with a view to their release Assessing deviations, change control, anomalies, OOX, CAPA, etc. Leading or contributing to the necessary risk analyses justifying the CMC development strategy Also participating in due diligence The products concerned may be injectables or dry forms. Requirements About You We are looking for a quality‑focused individual who is eager to contribute to our CMC projects while embracing the values that make Excelya unique. Preferably a Pharmacist or Engineer with experience in sterile products and dry forms, ideally in pharmaceutical development Experience: Experience in quality assurance, particularly in reviewing clinical or commercial files related to sterile products and dry forms. Skills: Proficiency in GMP (including Annexes 1 and 13) and ICH regulations Languages: Proficiency in English is required; French language skills are a plus. Benefits 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 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. At Excelya, Care lies at the heart of what we do. We provide equal opportunities for all and foster a diverse, equitable, and inclusive workplace where humility and boldness work hand in hand. Everyone has a space to feel valued, thrive, and collaborate with purpose. Your challenges become our shared mission. Together, we transform bold ideas into reality—the Excelya way. Apply today, become an Excelyate #J-18808-Ljbffr