Senior Manager CMC Regulatory Affairs

A company is looking for a Sr. Manager Global CMC Regulatory Affairs. Key Responsibilities Oversees deliverables for CMC strategy and submissions for an assigned portfolio of products Works with external stakeholders and seeks to influence regulatory policy globally Identifies regulatory risks across products and ensures aligned plans for mitigation Required Qualifications Doctorate degree and 2 years of experience in regulatory or pharmaceutical drug development, or Master's degree and 4 years of experience in regulatory or pharmaceutical drug development, or Bachelor's degree and 6 years of experience in regulatory or pharmaceutical drug development, or Associate's degree and 10 years of experience in regulatory or pharmaceutical drug development, or High school diploma/GED and 12 years of experience in regulatory or pharmaceutical drug development

Apr 2, 2025 - 00:22

A company is looking for a Sr. Manager Global CMC Regulatory Affairs. Key Responsibilities Oversees deliverables for CMC strategy and submissions for an assigned portfolio of products Works with external stakeholders and seeks to influence regulatory policy globally Identifies regulatory risks across products and ensures aligned plans for mitigation Required Qualifications Doctorate degree and 2 years of experience in regulatory or pharmaceutical drug development, or Master's degree and 4 years of experience in regulatory or pharmaceutical drug development, or Bachelor's degree and 6 years of experience in regulatory or pharmaceutical drug development, or Associate's degree and 10 years of experience in regulatory or pharmaceutical drug development, or High school diploma/GED and 12 years of experience in regulatory or pharmaceutical drug development