Senior Associate, Regulatory Affairs - Chemistry, Manufacturing & Control (CMC) - Hybrid

**Senior Associate, Regulatory Affairs - Chemistry, Manufacturing & Control (CMC) at AbbVie** **What you'll do** - Manage, compile, and author CMC sections of marketed product variations - Partner with RA CMC Project Leads to develop content plans and project timelines - Collaborate with functional groups to ensure file-ability of CMC sections - Ensure thoroughness, accuracy, and timeliness of CMC dossiers and responses **What they're looking for** - BA/BS Degree in Chemical, Biological Sciences or relevant discipline - 4 years pharmaceutical or industry related experience - 1-2 years in quality systems or cross functional project management - Experience in regulatory affairs preferred **Details** - Location: Waltham, United States (Hybrid: 3 days in office, 2 days remote) - Type: Full-time - Salary: null