This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Regulatory Affairs Associate based in India. Join a regulatory affairs team supporting the lifecycle management of medicinal products across European markets. In this role, you will contribute to post-approval regulatory activities, helping ensure products remain compliant throughout their lifecycle. You will assess the regulatory impact of manufacturing, quality, labeling, and product-information changes and support the development of appropriate regulatory strategies. The position combines regulatory expertise, CMC documentation, dossier management, and cross-functional collaboration. You will work with established regulatory systems and processes while helping identify and resolve documentation gaps and compliance risks. This is an opportunity to contribute to the continued availability and compliance of medicinal products in a collaborative, international life sciences environment.