South San FranciscoFull TimeHealthcare
Remotely
regulatory affairsregulatory intelligencelabelingms officeedmsrimglsdocx tool
Job Description
📋 Description
- Assist creation and maintenance of product labeling in global labeling systems (RIM/GLS).
- Support lifecycle management of product submissions and authorizations in RIM.
- Manage US SPL and CA XML-PM listings; participate in cross-functional teams.
- Train internal customers on Regulatory information issues.
- Provide SME support on labeling systems and processes; troubleshoot GLS RIM issues.
- Prepare routine communications for leadership with core labeling info.
🎯 Requirements
- Bachelor’s in life sciences or Associate degree with 8+ years related experience.
- 3+ years in regulatory affairs, R&D, or related area.
- Experience in a complex global matrix with strong communication and detail orientation.
- Preferred: electronic regulatory submissions, software tools, data standards, strategy role
🎁 Benefits
- AbbVie offers comprehensive benefits package; see posting for details.
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