AbbVie

Assist with creation and maintenance of labeling in RIM/global systems for products (Rx, OTC
Support lifecycle management of product submissions and authorizations in RIMGLS.
Manage US SPL and CA XML-PM listings and products in development.
Represent Regulatory Labeling-Operations in cross-functional meetings.
Provide guidance to internal customers on regulatory labeling issues.
Educate teams on regulatory information topics and ensure timely labeling responses.

🎯 Requirements

Bachelor’s in pharmacy, biology, chemistry, or related sciences; or Associate’s with 8+ years
3+ years in regulatory affairs, R&D, or related area.
Experience in global matrix environments with strong communication and attention to detail.
Experience with electronic submissions, software tools, and data standards; regulatory strategy

🎁 Benefits

Comprehensive benefits package
Opportunity for career development
Inclusive, diverse workplace

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