WalthamFull TimeOperations
Remotely
regulatory affairsregulatory intelligencelabelingms officeedmsrimglsdocx tool
Job Description
📋 Description
- Assist with creation and maintenance of product labeling in global labeling systems (RIM GLS).
- Support lifecycle management of product submissions, applications and authorizations in RIM.
- Manage US SPL and CA XML-PM drug listings and products in development.
- Serve as regulatory labeling operations representative on project teams.
- Collaborate with cross-functional groups and provide guidance on labeling processes.
- Educate internal customers on Regulatory information issues and ensure data accuracy.
🎯 Requirements
- Bachelor’s degree in life sciences or equivalent, or Associate’s degree with 8 years related
- 3+ years in regulatory affairs, R&D, or related area
- Experience in global matrix environment; strong communication and attention to detail
- Experience with electronic regulatory submissions, software tools, and data standards preferred
🎁 Benefits
- AbbVie is an equal opportunity employer with a comprehensive benefits package
- Short-term incentive programs eligibility
- PTO and medical/dental/vision insurance
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