A BDN client is looking for a CMC Regulatory Affairs Consultant who will be responsible for supporting the CMC Regulatory Affairs team in developing, coordinating, and implementing global CMC regulatory strategies for assigned programs and tasks. Specifically, the contractor will be supporting the CMC Regulatory Affairs team in defining and optimizing global organizational strategy pertaining to the development, registration, commercialization, and lifecycle management in the United States and international markets. This individual will proactively contribute to the development and implementation of innovative CMC regulatory strategies in close collaboration with the Lead, CMC Regulatory Affairs and relevant R&D and Commercial functions to obtain, maintain and extend product registrations in the United States, Japan, the European Union, Canada, and emerging markets. A minimum of 2-6 years of experience in global drug/Biologics development in the Biopharmaceutical or Biotechnology industry or Government Health Authorities is desired. A minimum of 2-5 years of experience in a Regulatory Affairs CMC role is essential to this role. Experience in plasma-derived therapies or Biologics is preferable, but not required for this role.