South San FranciscoFull TimeOperations
Remotely
data analyticsregulatory submissionslabelingms officeedmsrimgls
Job Description
📋 Description
- Assist creation and maintenance of product labeling in RIM/global labeling systems.
- Contribute to labeling for marketed products and lifecycle management of submissions.
- Provide guidance on labeling for US SPL/CA XML-PM and products in development.
- Represent Regulatory Labeling-Operations in cross-functional meetings.
- Educate internal customers on regulatory information issues across functions.
- Execute business processes for product information management within RIM/GLS systems.
🎯 Requirements
- Bachelor’s in life sciences or 8 years related experience; or Associate’s with relevant background.
- 3+ years in regulatory affairs, R&D, or related area.
- Experience in global matrix environments; strong communication and detail orientation.
- Preferred: experience with electronic regulatory submissions, software tools, data standards; prior
🎁 Benefits
- AbbVie offers a comprehensive benefits package including PTO, medical/dental/vision, and 401(k).
- Competitive compensation with potential for additional incentives.
- AbbVie is an equal opportunity employer; inclusive workplace commitments.
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