About this role
Quality Specialist Development (Leiden, NL) Pharming Group n.V. Quality Assurance Posted on Jul 30, 2026 Contribute to the development of innovative therapies for patients with rare diseases Are you an experienced Quality Assurance professional with a strong GMP background and experience in the pharmaceutical or biopharmaceutical industry? Would you like to play a key role in the development of innovative therapies that make a real difference in patients' lives worldwide? If so, we would love to hear from you. About Pharming Pharming is a global biotechnology company dedicated to developing innovative therapies for people living with rare diseases. Our mission is to improve patients' lives by addressing significant unmet medical needs. Quality, collaboration, and innovation are at the heart of everything we do. Your work environment As a Quality Specialist Development, you will be part of the Quality Assurance team within Pharming Technologies B.V. and serve as the dedicated QA Business Partner for one of our CMC Development Teams (Chemistry, Manufacturing & Controls). In this highly collaborative role, you will provide strategic quality oversight and expert guidance throughout the product lifecycle, from development and validation through technology transfer and commercialization. You will play a key role in influencing project decisions, and ensuring alignment with Pharming's quality standards and applicable EU and US GMP requirements. You will work closely with colleagues across QA, CMC, Manufacturing, QC, Regulatory Affairs, Supply Chain, and R&D, while also collaborating with external partners, including contract manufacturers, laboratories, and suppliers. What will you do? - Provide strategic QA guidance to the CMC Development Team throughout development, technology transfer and commercialization activities; - Support and review development, technology transfer, validation, and commercial manufacturing activities; - ...