Sr Regulatory CMC Consultant - Small Molecule & Veeva RIM Must Have

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Sr Regulatory CMC Consultant - Small Molecule & Veeva RIM Must Have based in Portugal. We are seeking an experienced Regulatory CMC Consultant to support regulatory affairs activities for small-molecule pharmaceutical products. In this senior consulting role, you will apply your expertise in regulatory requirements, drug development, and product lifecycle management to help ensure products remain compliant throughout their time on the market. You will assess regulatory guidelines, support ongoing regulatory obligations, and contribute to effective reporting and surveillance processes. Working in a collaborative, international life sciences environment, you will partner with cross-functional teams to address complex regulatory needs. This opportunity is suited to a knowledgeable professional who can combine strong technical judgment with clear communication and organized project execution.