Regulatory Documentation Specialist (Contract) – QC & Formatting

A biopharmaceutical company in Florham Park seeks a Regulatory Operations Documentation Specialist Contract to format documents to Shionogi standards. This role supports varying regulatory activities, including remediation efforts, to ensure compliance with electronic submissions. Candidates should possess at least 2 years in regulatory affairs within pharma/biotech, strong detail orientation, and proficiency in MS Office and Adobe. The role offers an hourly rate of $40-$57 and fosters a high-performance collaborative team environment. #J-18808-Ljbffr