Parexel seeks a Regulatory Affairs Consultant (CMC/Technical Regulatory Specialist) to join our team in a remote capacity. You will support post-approval regulatory activities, shaping CMC regulatory strategy, ensuring compliance, and driving accurate submissions across global markets.
You’ll collaborate with manufacturing, quality, and supply chain partners to plan submissions, assess changes, and manage regulatory information systems, advancing clinical product development and market expansion.
#J-18808-LjbffrRemote Post-Approval CMC Regulatory Strategist in carson city at Unknown Company
This position is listed as full time and able to be worked remotely.