experience including 1-2 years in regulatory affairs, R&D, or Manufacturing (CTD Module 3) RA Associate Responsible... of regulatory filings. Manage, compile, and author CMC sections of marketed product variations including CTD content, structural...
Experience is 5 years pharmaceutical experience including 1-2 years in regulatory affairs, R&D, or Manufacturing (CTD Module 3...). Regulatory submission documentation creation background. Detail/accuracy oriented, collaborative and willing to learn...