CMC Regulatory Affairs Manager — Lisbon

We are hiring a CMC Regulatory Affairs Manager for a multinational pharmaceutical company based in Lisbon. In this role, you will be responsible for planning, preparing, revising, and maintaining regulatory CMC documentation for designated products. You will also develop global CMC strategies in collaboration with internal and external stakeholders, offer regulatory guidance to manufacturing sites, suppliers, and partners, and support product lifecycle management. Additionally, you will assess product changes, identify risks and mitigation strategies, and collaborate closely with cross-functional teams and external partners to ensure alignment on product and process changes.